A multiplex CRISPR / Cas9-mediated targeted gene activation system

Abstract

Provided herein are multiple crRNAs and multiple sgRNAs, and RNA molecules thereof.Also provided are compositions and kits that include multiple crRNAs and sgRNAs, which can be used in multiple targeted gene activation (mTGA) systems.Also provided are methods that include administering a therapeutically effective amount of the mTGA system to a subject.In some examples, the methods treat diseases associated with reduced or non-expression of genes, such as type I diabetes, Duchenne muscular dystrophy, liver disease, or acute kidney disease.

Description

[Technical field]

[0001] CROSS-REFERENCE TO RELATED APPLICATIONS This claims the benefit of U.S. Provisional Application No. 63 / 181,059, filed April 28, 2021, which is incorporated herein by reference.

[0002] Field The present application provides multiple CRISPR RNAs (crRNAs) and multiple single guide RNAs (sgRNAs), as well as compositions and kits comprising multiple crRNAs and multiple sgRNAs, which can be used in multiple targeted gene activation (mTGA) systems, for example, to increase expression of genes, reprogram cells, or treat diseases in vivo. [Background technology]

[0003] background Duchenne muscular dystrophy (DMD) is a fatal muscle-wasting disease and one of the most frequent genetic disorders worldwide, affecting 1 in 3,500–5,000 male births. DMD results in progressive muscle weakness, eventually resulting in respiratory and cardiac failure in the teenage years (Blake et al. (2002) Physiological Reviews 82:291-329). DMD is caused by frameshift mutations in the dystrophin gene, with at least 726 different mutations identified throughout the coding region (Bladen et al. (2015) Hum Mutat 36:395-402). Within this gene, there are several mutational "hotspots," including exons 45–53, of which exon 51 is the most frequently mutated, accounting for approximately 13% of DMD cases. Currently, there is no effective treatment for DMD, and transplantation of muscle stem cells into damaged organs to halt disease progression has proven difficult. Due to the large size of the dystrophin gene (the cDNA is approximately 14 kb), it has also proven difficult to deliver a functional dystrophin transgene to affected tissues via traditional viral-mediated gene therapy (Janghra et al. (2016) PloS one 11, e0150818; Sicinski et al. (1989) Science 244: 1578-1580).

[0004] Recently, several groups have restored dystrophin gene function by using CRISPR / Cas9 technology to remove the mutated exon, thereby creating a truncated but functional version of the dystrophin gene (Amoasii et al.(2018) Science 362:86-91; Amoasii et al.(2017) Sci Transl Med 29:9(418); Bengtsson et al.(2017) Nat Commun 14:8,14454; Long et al.(2016) Science 351:400-403; Moretti et al.(2020) Nat Med 26:207-214; Nelson et al.(2016) Science 351:403-407; Nelson et al.(2019) Nat Med 25:427-432; Tabebourdbar ... al.(2016) Science 351:407-411; Zhang et al.(2017) Sci Adv 3,e1602814). Although this method shows promise, some exons within the dystrophin gene are important for protein function and cannot be removed to cure the disease. Only 55% of DMD patients could potentially benefit from these exon skipping / excision therapies (Bladen et al.(2015) Hum Mutat 36:395-402). Thus, there is a need for alternative approaches to restore muscle function in DMD, particularly approaches that are effective regardless of which dystrophin mutation a patient carries.

[0005] Utrophin is a functional analog of dystrophin and therefore likely can compensate for the loss of dystrophin in DMD patients (Rafael et al. (1998) Nat Gen 19,79-82; Tinsley et al. (1996) Nature 384:349-353). Therefore, a potential treatment strategy is to upregulate utrophin in DMD patients. Instead of inducing double-strand breaks in the target DNA, the CRISPR / Cas9 system can be modified to induce targeted gene expression by recruiting a transcription activation domain to the target promoter region (Qi et al. (2013) Cell 152:1173-1183; Liao et al. (2017) Cell 171:1495-1507 e1415). However, a major obstacle in implementing this system for the treatment of DMD is that utrophin induction by the CRISPR / Cas9 gene activation system is limited and a more robust system is needed. [Prior art documents] [Non-patent literature]

[0006] [Non-Patent Document 1] Blake et al. (2002)Physiological Reviews 82:291-329 [Non-Patent Document 2] Bladen et al. (2015) Hum Mutat 36:395-402 [Non-Patent Document 3] Janghra et al.(2016)PloS one 11,e0150818 [Non-Patent Document 4] Sicinski et al. (1989) Science 244:1578-1580 [Non-Patent Document 5] Amoasii et al. (2018) Science 362:86-91 [Non-Patent Document 6] Amoasii et al. (2017) Sci Transl Med 29:9(418) [Non-Patent Document 7] Bengtsson et al. (2017) Nat Commun 14:8,14454 [Non-Patent Document 8] Long et al. (2016) Science 351:400 - 403 [Non-Patent Document 9] Moretti et al. (2020) Nat Med 26:207 - 214 [Non-Patent Document 10] Nelson et al. (2016) Science 351:403 - 407 [Non-Patent Document 11] Nelson et al. (2019) Nat Med 25:427 - 432 [Non-Patent Document 12] Tabebordbar et al. (2016) Science 351:407 - 411 [Non-Patent Document 13] Zhang et al. (2017) Sci Adv 3,e1602814 [Non-Patent Document 14] Rafael et al. (1998) Nat Gen 19,79 - 82 [Non-Patent Document 15] Tinsley et al. (1996) Nature 384:349 - 353 [Non-Patent Document 16] Qi et al. (2013) Cell 152:1173 - 1183 [Non-Patent Document 17] Liao et al. (2017) Cell 171:1495 - 1507 e1415 [Summary of the Invention] [Means for Solving the Problems]

[0007] Summary Provided herein are nucleic acid molecules (such as DNA molecules) encoding multiple CRISPR RNAs (crRNAs) and multiple single guide RNAs (sgRNAs). The encoded multiple crRNAs include a first promoter operably linked to a nucleic acid molecule encoding a modified trans-activating CRISPR RNA (tracrRNA), a first cleavage site, a first nucleic acid molecule encoding the first crRNA, a second cleavage site, and a second nucleic acid molecule encoding the second crRNA. The modified tracrRNA encodes at least two modified MS2 binding loops. In some embodiments, the encoded multiple crRNAs further include a second promoter operably linked to a third nucleic acid molecule encoding a crRNA or a dead guide RNA (dgRNA). In some examples, the second promoter and the third crRNA (or dgRNA) are in a reverse orientation relative to the first promoter. In some examples, the second promoter and the third crRNA (or dgRNA) are located 5' of the first promoter. In some examples, the first cleavage site is a pre-transfer RNA (pre-tRNA) and the second cleavage site is a self-cleaving ribozyme, such as a hammerhead ribozyme. In further examples, the crRNA, sgRNA or dgRNA disclosed herein comprises a targeting sequence complementary to a sequence within the promoter region of EEF1α2 (eukaryotic translation elongation factor 1α2), Fst (follistatin), Pdx1 (pancreatic and duodenal homeobox 1), Klotho, utrophin, interleukin 10, or Six2 (SIX homeobox 2).

[0008] Also provided herein are nucleic acids (such as DNA molecules) encoding multiple single guide RNAs (sgRNAs). The multiple sgRNA comprises a first nucleic acid molecule encoding a first modified sgRNA in a reverse orientation operably linked to a first promoter, and a second nucleic acid molecule encoding a second modified sgRNA in a forward orientation operably linked to a second promoter. The first and second modified sgRNAs encode at least two modified MS2 binding loops. In some embodiments, the multiple sgRNA further comprises a third nucleic acid molecule located 3' of the second nucleic acid molecule, the third nucleic acid encoding a first cleavage site and a third modified sgRNA in a forward orientation. In some embodiments, the multiple sgRNA further comprises a fourth nucleic acid molecule located 5' of the first nucleic acid molecule, the fourth nucleic acid molecule encoding a second cleavage site and a fourth modified sgRNA in a reverse orientation. The third and fourth modified sgRNAs encode at least two modified MS2 binding loops. In some examples, the first and / or second cleavage sites encode pre-tRNA. In some examples, the sgRNA disclosed herein comprises a targeting sequence that is complementary to a sequence in the promoter region of EEF1α2, Fst, Pdx1, Klotho, utrophin, interleukin-10 or Six2. In some examples, the sgRNA is a dgRNA.

[0009] Also provided are RNA molecules encoded by the disclosed nucleic acids, and vectors comprising the disclosed nucleic acids (such as nucleic acids encoding multiple crRNAs or multiple sgRNAs), e.g., viral vectors, e.g., AAV vectors, such as AAV9 vectors. Also provided are compositions comprising the disclosed nucleic acids, or the RNA molecules thereof, or the disclosed vectors, and a pharma- ceutically acceptable carrier.

[0010] Kits comprising the disclosed nucleic acids, RNA, compositions, or viral vectors, as well as nucleic acids encoding Cas9 proteins or dead Cas9 (dCas9) proteins, and / or nucleic acids encoding MS2 transcription activator fusion proteins, are also provided.

[0011] A multiple targeted gene activation (mTGA) system is also provided. The system may include a first vector (e.g., a viral vector, e.g., AAV9) that includes a nucleic acid encoding Cas9 or dCas9, and a second vector (e.g., a viral vector, e.g., AAV9) that includes a nucleic acid disclosed herein (e.g., a nucleic acid encoding multiple crRNAs or multiple sgRNAs) and a nucleic acid encoding an MS2 transcription activator fusion protein (e.g., MS2-p65-HSF1).

[0012] Methods of using the disclosed nucleic acids, RNA, compositions, viral vectors, kits and mTGA systems are also provided. The methods include administering a therapeutically effective amount of the disclosed mTGA system to a subject. In some examples, the methods increase the expression of at least one target gene in a subject, thereby increasing the expression of at least one gene product. In some examples, the methods treat a disease in a subject caused by or associated with reduced or non-expression of a gene. In some examples, the target gene is a gene (causative gene) whose reduced expression causes the disease. In further examples, the target gene is a functional analog of the causative gene, and expression of the functional analog compensates for the loss of function of the causative gene. In some examples, the disease is muscular dystrophy, the causative gene is dystrophin, and the target gene is utrophin. In some examples, the disease is liver fibrosis or cirrhosis, and the target gene is Foxa3, Gata4, HNF1a and / or HNF4a.

[0013] The above and other objects and features of the present disclosure will become more apparent from the following detailed description which proceeds with reference to the accompanying drawings. [Brief description of the drawings]

[0014] [Figure 1] FIG. 1 shows an exemplary coding multiple CRISPR RNA (crRNA) construct 100 containing two crRNAs 101, 102. [Diagram 2]2A-2B show an exemplary coding multiple crRNA construct 100, comprising two crRNAs and a third nucleic acid molecule 103 encoding a third crRNA or dgRNA operably linked to a second promoter 111. The third nucleic acid molecule 103 can be located 3' of the second crRNA (FIG. 2A) or 5' of the first promoter (FIG. 2B). In some embodiments, the third nucleic acid molecule is located 5' of the first promoter and in a reverse orientation relative to the first promoter (FIG. 2B). [Diagram 3] Figures 3A-3E show an exemplary coding multiplex single guide RNA (sgRNA) construct 200. Figures 3A, 3C, and 3D show an exemplary DNA construct containing two sgRNAs. Figures 3B and 3E show an exemplary DNA construct containing three sgRNAs. [Figure 4] FIG. 4 shows an exemplary coding multiplex single guide RNA (sgRNA) construct 200 containing four sgRNAs. [Diagram 5] FIG. 5 shows utrophin activation of dgRNAs targeting different regions of the utrophin locus (sequence shown is SEQ ID NO: 56). [Figure 6] Figure 6A shows activation of utrophin (Utrn) analyzed by qRT-PCR 2 days after transfection. Cas9-expressing N2a (N2aCas9) cells were transfected with the indicated combinations of utrophin targeting dgRNA and plasmid containing MPH. Figure 6B shows dgRNA activation of Eef1a2 expression. [Figure 7] Figure 7 shows Western blot (top) and relative protein levels (bottom) of Utrn in N2aCas9 cells. The combination of dgEef1a2 and dgUtrnNT2 significantly enhances the upregulation of utrophin. [Figure 8] FIG. 8 shows a schematic diagram of AAV vectors containing one sgRNA (top) or multiple sgRNAs (middle and bottom). [Figure 9]Figure 9 shows the efficiency of different promoters in mouse N2 cells. Cas9-expressing N2a (N2aCas9) cells were transfected with the indicated plasmids and a plasmid containing MPH. Activation of Fst was analyzed by qRT-PCR 2 days after transfection. [Figure 10] FIG. 10 shows the activation efficiency of UtnNT2, Eef1α2, and MyoD using the hU6, mU6, H1, or 7SK promoters. [Figure 11] FIG. 11 shows targeted induction of gene expression using a two-multiplexed sgRNA system where the second sgRNA (dgFst) is in the forward (circle) or reverse (square) orientation relative to the first sgRNA (dgUtrn). [Figure 12] Figure 12 shows a schematic (top) and gel electrophoresis image (bottom) of the recombination that occurs when both sgRNAs are in the forward orientation. The presence of a "low band" in the gel confirms the presence of an undesired recombination product when both sgRNAs are in the forward orientation. Recombination was verified by Sanger sequencing (see Figure 13). Blue arrows indicate the primer positions for PCR amplification. [Figure 13] Figure 13 shows Sanger sequencing confirming the presence of the recombinant product. The top sequence is SEQ ID NO:57 and the bottom sequence is SEQ ID NO:58. [Figure 14] Figure 14 shows a schematic of duo-dgRNA using direct repeat (DR) or inverse repeat (IR) orientation. The fold activation of target genes by duo-dgRNA in DR (circle) or IR (square) orientation is shown below. [Figure 15] FIG. 15 shows that when the duo-dgRNA is in the direct repeat orientation, a truncated product is produced, indicating undesired recombination. [Figure 16] Figure 16 shows a schematic diagram of a skeletal muscle-specific mTGA construct with a duo-dgRNA oriented as an inverted repeat. Below is an exemplary design for in vivo experiments. [Figure 17] Figure 17 shows myofiber damage in TA muscles as indicated by EBD uptake. Damaged myofibers accumulate EBD and therefore show more fluorescence. TA muscle mass is also shown (top right). [Figure 18] Figures 18A and 18B show the expression of targeted genes. Figure 18A shows that AAV9-dgUtrnT2-dgFst-MPH treatment increased the expression of utrophin and Fst by 1.8-fold and 10-fold, respectively. Figure 18B shows that AAV9-dgUtrnNT2-dgEef1a2-MPH treatment increased the expression of utrophin and Eef1a2 by 2.6-fold and 2.2-fold, respectively. [Figure 19] Figure 19 shows Western blots (left) and relative protein levels (right) after in vivo treatment. The results show that AAV9-dgUtrnNT2-dgEef1a2-MPH(UE) treatment upregulated utrophin expression by 3.7-fold, while AAV9-dgUtrnT2-dgFst-MPH(UT) treatment upregulated utrophin by 1.5-fold. [Figure 20] FIG. 20 shows immunostaining for utrophin. [Figure 21] Figure 21 shows a schematic diagram of three multiplex sgRNAs driven by three individual RNA polymerase III promoters. Gel electrophoresis shows that undesired recombination occurred in the construct with three promoters (lower band). Blue arrows indicate the primer positions for amplification. Recombination was verified by Sanger sequencing (see Figure 22). [Figure 22] Figure 22 shows Sanger sequencing confirming unwanted recombination products in a construct with three promoters. The sequence shown is SEQ ID NO:59. [Diagram 23] Figure 23 shows a comparison of fold activation using a system with two individual promoters driving the expression of two gRNAs (bottom schematic), or a system with one promoter driving the expression of two gRNAs separated by a tRNA (top schematic). [Figure 24]Figure 24 compares gene activation with the indicated constructs using N2aCas9 cells. [Diagram 25] Figure 25 shows a comparison of recombination of two sgRNA systems with either two promoters (top schematic) or one promoter and tRNA cleavage site (bottom schematic). Gel electrophoresis and real-time qPCR results show that less recombination occurred in the construct containing one promoter with tRNA. Blue arrows indicate primer positions for amplification. [Figure 26] FIG. 26 shows the activation efficiency of hU6-tRNA and hU6-H1 constructs. [Figure 27] FIG. 27 shows a gel electrophoresis image showing that the hU6-tRNA construct had fewer recombination events than the hU6-H1 construct. [Figure 28] FIG. 28 shows the qPCR results of the ratio of tRNA or H1 to hU6 in plasmids and AAV recovered from C2C12Cas9 cells. [Figure 29] FIG. 29 shows efficient activation of MyoD, Mef2b and Pax7 in 3T3L1Cas9 cells treated with the indicated mTGA constructs (containing dgMyoD, dgMef2b and dgPax7). [Diagram 30] Figure 30 shows a comparison between the UtrnT2 TGA system (one sgRNA) and the UtrnTriple multiplex TGA (mTGA) system (three sgRNAs). N2aCas9 cells were transfected with AAV vectors containing the single TGA (UtrnT2) and mTGA (UtrnTriple) systems. Activation of utrophin was analyzed by qRT-PCR two days after transfection. C2C12 Cas9 cells were transduced with AAVs containing the single and mTGA systems. Activation of utrophin was analyzed by qRT-PCR 10 days after transfection. [Diagram 31] FIG. 31 shows that the multiplex TGA system simultaneously activates the expression of multiple genes in the tibialis anterior (TA) muscle of Cas9+Mdx mice. [Diagram 32] FIG. 32 shows gene activation using an mTGA construct containing four gRNAs. [Diagram 33] Figures 33A-33B show that the mTGA system enhances utrophin expression in vivo. Figure 33A: Cas9-expressing WT mice were injected with AAV containing single gRNA TGA (UtrnT2) or mTGA (UtrnTriple) systems. Two months after injection, utrophin activation was analyzed by qRT-PCR (n=5). Figure 33B: Western blot analysis of utrophin in tibialis anterior (TA) muscles injected with AAV containing single TGA (gUtrnT2-MPH), mTGA (gUtrnTriple-MPH), or MPH only. Hsp90 is a loading control. [Diagram 34] Figures 34A-34B show RNA-seq analysis of tibialis anterior (TA) muscles injected with AAVs containing gUtrnTriple-MPH or MPH alone (Figure 34A). Figure 34B shows immunostaining of utrophin in TA muscles injected with the indicated AAVs. Scale bar = 50 μm. [Diagram 35] Figure 35 shows the experimental design of the grip strength assay (top) and grip strength (bottom) of the indicated mice receiving the indicated AAV treatments. Sixty consecutive grip strength trials were performed for each mouse. Leads were averaged every 10 trials. [Diagram 36] FIG. 36 shows the assessment of sarcolemma integrity by intraperitoneal injection of EBD in mice receiving the indicated treatments. EBD accumulates in damaged cells. Two hours after EBD injection, mice were subjected to treadmill running for 2 min at a speed of 6 m / min, followed by 2 min of rest. Treadmill running was repeated three times. High levels of EBD uptake indicate muscle damage. Treatment with the mTGA system (UtrnTriple) significantly improved the disconnection of muscle fibers during contraction. [Figure 37]Figure 37 shows that the mTGA system enhances the expression of utrophin in Mdx mice. Cas9-expressing Mdx mice were injected with AAV containing single sgRNA TGA system (UtrnT2) or mTGA system (UtrnTriple). Two months after injection, the activation of utrophin was analyzed by qRT-PCR (n=4). [Figure 38] Figure 38 shows Cas9-expressing Mdx mice injected with AAVs containing the single sgRNA TGA system (UtrnT2) or the mTGA system (UtrnTriple). Immunostaining of utrophin in TA muscles injected with the indicated AAVs. [Figure 39] Figure 39 shows EBD uptake into the TA muscle of mdx mice 2 months after mTGA treatment. Extensive EBD uptake was found in control-treated mdx mice, but EBD uptake is significantly attenuated in mTGA-treated mice. Furthermore, Utrn immunostaining confirms utrophin activation. [Diagram 40] Figures 40A and 40B show quantification of utrophin expression by qPCR (Figure 40A) and Western blot (Figure 40B) in TA muscles treated with control (MPH) and the mTGA system (UtrnTriple). [Diagram 41] Figure 41A shows the experimental design. TA muscles of Cas9 / mdx mice are injected with 1x1011 GC AAV9-MPH, AAV9-hU6-dgUtrnT2-MPH, AAV9-UtrnDual, or AAV9-UtrnTriple. Figure 41B shows the mRNA levels of utrophin 2 months after AAV injection. [Diagram 42] FIG. 42 shows chromatin immunoprecipitation (ChIP) qRT-PCR of TA muscle samples. [Diagram 43] FIG. 43 shows chromatin immunoprecipitation (ChIP) qRT-PCR of TA muscle samples. [Diagram 44]Figure 44A shows the experimental design. The TA muscle of idCas9 mice was co-injected with AAV containing a luciferase reporter in which luciferase was placed downstream of the dgRNA (dgLuc) binding site and AAV containing a dgLuc-CAG-MPH sequence. Then, Dox water (1 mg / ml) was added and removed at intervals of 1 week or 2 weeks. Figure 44B shows that the luciferase signal was induced 1 week after Dox administration and returned to basal levels 2 weeks after administration. [Diagram 45] Figure 45 shows endogenous activation of utrophin in idCas9 mice injected with 1x1011 GC AAV9-UtrnTriple or AAV9-MPH. Mice were administered 30 consecutive days of Dox (30 On), 60 consecutive days of Dox (60 On), or 30 days without Dox (30 Off) followed by 30 consecutive days of Dox. [Figure 46] Figure 46A shows the experimental design for co-injection of AAV9-dCas9 and AAV9-UtrnTriple or AAV9-MPH. Muscle samples were collected after 13 months of treatment. Figure 46B shows that a three-fold increase in utrophin was observed in samples treated with the mTGA system. Figure 46C shows the immunostaining of utrophin, verifying Utrn activation. [Figure 47] Figures 47A and 47B show H&E staining (Figure 47A) and Mallory's trichrome staining (Figure 47B) to assess the histopathological phenotype of muscle samples. [Figure 48] Figure 48 shows the dgUtrnNT2-Eef1a2, dgUtrnNT2-dgUtrnT2-dgUtrnT16 (UtrnTriple), and UtrnDual-Eef1a2 mTGA constructs. [Figure 49] Figure 49A shows the expression of Eef1a2 and utrophin in the TA muscle of mdx mice after 2 months of treatment with dgUtrnNT2-Eef1a2, UtrnTriple, UtrnDual-Eef1a2, or MPH. Figure 49B shows Utrn protein levels. [Figure 50]Figure 50A is a schematic diagram showing intramuscular injection of MPH or dual AAV systems into multiple muscles of 2-month-old mdx mice. Figure 50B shows serum creatine kinase activity 2 months after AAV treatment. [Figure 51] Figures 51A and 51B show that mTGA treatment increases activity and endurance in mdx mice compared to control mice (MPH). Figure 51A shows the results of the open field test. Figure 51B shows the results of the treadmill test. [Figure 52] Figure 52 shows a sequencing map showing that recombination in the single promoter tRNA construct occurs between the first and fourth MS2 loops. Unlabeled bars indicate MS2 loops. The top sequence is SEQ ID NO:60 and the bottom sequence is SEQ ID NO:61. [Figure 53] Figures 53A and 53B show the activation of target genes using CRISPR RNA (crRNA) and a modified transactivating CRISPR RNA (tracrRNA-M2) containing two MS2 loops. Although the crRNA-tRNA-tracrRNA-M2 construct could activate target genes, its activation efficiency was 2.8-fold lower than that of dgRNA (Figure 53A). When the two crRNAs were driven by two different U6 promoters, only the crRNA that shared the same promoter as tracrRNA-M2 had strong activation efficiency (Figure 53B). [Figure 54] Figure 54 shows the design and testing of an alternative mTGA system utilizing tRNA and / or hammerhead RNA between the tracrRNA and crRNA elements. Gene 1 is Fst and gene 2 is utrophin. [Figure 55] FIG. 55 shows gel electrophoresis demonstrating that no recombination occurs in a construct containing tracrRNAM2 and two crRNA1 (crFst) and crRNA2 (crUtrn). [Figure 56]Figure 56A shows that the activation efficiency of AAVDJ-hU6-tracrRNA-M2-tRNA-crFst-HDV-HH-crUtrn-MPH is not higher than that of AAVDJ-hU6-dgUtrnT2-tRNA-dgFst-MPH in C2C12Cas9 cells. Figure 56B shows the in vivo activation of utrophin 2 months after intramuscular injection of different concentrations of AAV9-MPH, AAV9-UtrnTriple, or AAV9-UtrnTriple-crRNA into the TA muscle of Cas9 / mdx mice. [Figure 57] Figure 57 shows luciferase expression to follow the distribution of AAV after tail vein injection at the indicated titers. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0015] Sequence Listing Any nucleic acid and amino acid sequences listed herein or in the attached sequence listing are shown using standard letter abbreviations for nucleotide bases and amino acids as defined in 37 CFR § 1.822. In at least some cases, only one strand of each nucleic acid sequence is shown, but the complementary strand is understood to be included by any reference to the displayed strand. The sequence listing is submitted as an 81,920 byte ASCII text file "Sequence.txt", created on April 27, 2022, which is incorporated herein by reference. In the attached sequence listing:

[0016] SEQ ID NO:1 is an exemplary DNA sequence encoding the tracrRNA-tRNA-UT2-HH-UT16 multiple crRNA. [ka]

[0017] SEQ ID NO:2 is an exemplary DNA sequence encoding the dgUtnNT2-mU6-hU6-tracrRNA-tRNA-crUT2-HH-crUT16 multiple crRNA together with a dgRNA ("UtrnTriple-crRNA"). [ka] [ka]

[0018] SEQ ID NO:3 is an exemplary DNA sequence encoding the dgFst / dgUtrn multiple sgRNA. [ka]

[0019] SEQ ID NO:4 is an exemplary DNA sequence encoding a dgUtnNT2 / dgUtrnT2 / dgUtrnT16 multiple sgRNA ("UtrnTriple"). [ka] [ka]

[0020] SEQ ID NO:5 is an exemplary DNA sequence encoding dgUtnNT2-mU6-hU6-dgFst-tRNA-dgEef1a2 multiple sgRNAs. [ka]

[0021] SEQ ID NO:6 is an exemplary DNA sequence encoding the dgFst / dgEef1a2 / dgUtnNT2 / dgUtrnT2 multiple sgRNA. [ka] [ka]

[0022] SEQ ID NO:7 is an exemplary DNA sequence encoding a modified tracrRNA. [ka]

[0023] SEQ ID NO:8 is an exemplary DNA sequence encoding crUT2. [ka]

[0024] SEQ ID NO:9 is an exemplary DNA sequence encoding crUT16. [ka]

[0025] SEQ ID NO:10 is an exemplary DNA sequence encoding a dgFST. [ka]

[0026] SEQ ID NO:11 is an exemplary DNA sequence encoding dgEef1α2. [ka]

[0027] SEQ ID NO: 12 is an exemplary DNA sequence encoding dgUtrnNT2. [ka]

[0028] SEQ ID NO:13 is an exemplary DNA sequence encoding dgUtrn. [ka]

[0029] SEQ ID NO:14 is an exemplary DNA sequence encoding dgUtrnT2. [ka]

[0030] SEQ ID NO:15 is an exemplary DNA sequence encoding dgUtrnT16. [ka]

[0031] SEQ ID NO:16 is an exemplary DNA sequence encoding a native MS2 binding loop. [ka]

[0032] SEQ ID NO:17 is an exemplary DNA sequence encoding a modified MS2 binding loop. [ka]

[0033] SEQ ID NO:18 is an exemplary DNA sequence encoding a modified MS2 binding loop. [ka]

[0034] SEQ ID NO:19 is an exemplary DNA sequence encoding a modified MS2 binding loop. [ka]

[0035] SEQ ID NO:20 is an exemplary DNA sequence encoding a pre-tRNA of Saccharomyces cerevisiae. [ka]

[0036] SEQ ID NO:21 is an exemplary DNA sequence encoding a Zea mays pre-tRNA. [ka]

[0037] SEQ ID NO:22 is an exemplary DNA sequence encoding a hammerhead RNA. [ka]

[0038] SEQ ID NO:23 is an exemplary DNA sequence encoding the proximal promoter of human EEF1α2. [ka] [ka]

[0039] SEQ ID NO:24 is an exemplary DNA sequence encoding the proximal promoter of human Fst. [ka]

[0040] SEQ ID NO:25 is an exemplary DNA sequence encoding the proximal promoter of human Pdx1. [ka]

[0041] SEQ ID NO:26 is an exemplary DNA sequence encoding the proximal promoter of human Klotho. [ka]

[0042] SEQ ID NO:27 is an exemplary DNA sequence encoding the proximal promoter of human utrophin. [ka]

[0043] SEQ ID NO:28 is an exemplary DNA sequence encoding the proximal promoter of human interleukin-10. [ka]

[0044] SEQ ID NO:29 is an exemplary DNA sequence encoding the proximal promoter of human six2. [ka]

[0045] SEQ ID NO:30 is an exemplary DNA sequence encoding Cas9. [ka] [ka]

[0046] SEQ ID NO:31 is an exemplary Cas9 amino acid sequence. [ka] [ka]

[0047] SEQ ID NO:32 is an exemplary DNA sequence encoding dCas9. [ka] [ka]

[0048] SEQ ID NO:33 is an exemplary dCas9 amino acid sequence. [ka]

[0049] SEQ ID NO:34 is an exemplary DNA sequence encoding an MS2 transcriptional activator fusion protein. [ka] [ka]

[0050] SEQ ID NO:35 is an exemplary MS2-p65-HSF1 amino acid sequence. [ka]

[0051] SEQ ID NO:36 is an exemplary DNA sequence encoding the 7SK promoter. [ka]

[0052] SEQ ID NO:37 is an exemplary DNA sequence encoding the Spc5.12 promoter. [ka]

[0053] SEQ ID NO:38 is an exemplary DNA sequence encoding the Col1a2 promoter. [ka]

[0054] SEQ ID NO:39 is an exemplary DNA sequence encoding the mU6 promoter. [ka]

[0055] SEQ ID NO:40 is an exemplary DNA sequence encoding the hU6 promoter. [ka]

[0056] SEQ ID NO:41 is an exemplary DNA sequence encoding the H1 promoter. [ka]

[0057] SEQ ID NO:42 is an exemplary DNA sequence encoding dgMyoD. [ka]

[0058] SEQ ID NO:43 is an exemplary DNA sequence encoding dgMef2b. [ka]

[0059] SEQ ID NO:44 is an exemplary DNA sequence encoding dgPax7. [ka]

[0060] SEQ ID NO:45 is an exemplary DNA sequence encoding dgOCT4. [ka]

[0061] SEQ ID NO:46 is an exemplary DNA sequence encoding dgSOX2. [ka]

[0062] SEQ ID NO:47 is an exemplary DNA sequence encoding dgKLF. [ka]

[0063] SEQ ID NO:48 is an exemplary DNA sequence encoding dgMYC. [ka]

[0064] SEQ ID NO:49 is an exemplary DNA sequence encoding crUCP1. [ka]

[0065] SEQ ID NO:50 is an exemplary DNA sequence encoding crPgc1a. [ka]

[0066] SEQ ID NO:51 is an exemplary DNA sequence encoding a crFST. [ka]

[0067] SEQ ID NO:52 is an exemplary DNA sequence encoding crUtrn. [ka]

[0068] SEQ ID NO:53 is an exemplary DNA sequence encoding dgUtrnNT2-mU6-hU6-dgUtrnT2 ("UtrnDual"). [ka]

[0069] SEQ ID NO:54 is an exemplary DNA sequence encoding dgUtrnNT2-mU6-hU6-dgEef1a2 ("UtrnNT2-Eef1a2"). [ka] [ka]

[0070] SEQ ID NO:55 is an exemplary DNA sequence encoding dgUtrnT2-tRNA-dgUtrnNT2-mU6-hU6-dgEef1a2 ("UtrnDual-Eef1a2"). [ka]

[0071] SEQ ID NO:56 is the sequence shown in FIG. [ka]

[0072] SEQ ID NO:57 is the sequence of the upper band shown in FIG. [ka]

[0073] SEQ ID NO:58 is the sequence of the lower band shown in FIG. [ka]

[0074] SEQ ID NO:59 is the sequencing product shown in FIG. [ka]

[0075] SEQ ID NO:60 is the sequence product shown in Figure 52 (top). [ka]

[0076] SEQ ID NO:61 is the sequence product shown in Figure 52 (bottom). [ka]

[0077] Detailed Description The following explanations of terms and methods are provided to better describe the present disclosure and guide those skilled in the art in the practice of the present disclosure. The term "or" refers to a single element or a combination of two or more elements of the listed alternative elements, unless the context clearly indicates otherwise. As used herein, "comprises" means "includes." Thus, "comprises A or B" means "includes A, B, or A and B" without excluding additional elements.

[0078] Unless otherwise explained, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this disclosure belongs. Definitions of many common terms in molecular biology can be found in Krebs et al. (eds.), Lewin's genes XII, published by Jones&Bartlett Learning,2017. All references, including patent applications and patents, and sequences associated with the provided GenBank® accession numbers (as of April 28, 2021) are incorporated herein by reference in their entirety. Although methods and materials similar or equivalent to those described herein can be used in the practice or testing of this disclosure, suitable methods and materials are described below. All percentages and ratios are calculated by weight unless otherwise indicated. The term "about" refers to ±5% of the reference value. For example, "about" 100 refers to 95 to 105.

[0079] In case of conflict, the present specification, including explanations of terms, will control.Furthermore, the materials, methods, and examples are illustrative only and not intended to be limiting.

[0080] In order to facilitate review of the various embodiments of the disclosure, the following explanations of specific terms are provided:

[0081] I. Terminology Administration: Providing or giving to a subject an agent, such as the disclosed multiple target gene activation (mTGA) system or a portion thereof (e.g., multiple crRNAs or multiple sgRNAs, which may be part of a viral vector, or a nucleic acid encoding said RNAs, etc.), by any effective route. Administration can be local or systemic. Exemplary routes of administration include, but are not limited to, oral, injection (e.g., subcutaneous, intramuscular, intradermal, intraperitoneal, intrahepatic, transdermal (intracerebrovascular), and intravenous), sublingual, rectal, transdermal (e.g., topical), intranasal, vaginal, and inhalation routes. In some embodiments, administration is by injection.

[0082] Adeno-associated virus (AAV): A small, non-enveloped virus that can infect humans and some other primates. It can infect both non-dividing and dividing cells. AAV vectors can be used as gene therapy vectors, for example, to deliver nucleic acid molecules to target genes using the disclosed mTGA system and related methods. Exemplary AAV vectors that can be used in the methods and compositions provided herein include AAV1, AAV2, AAV3, AAV4, AAV5, AAV6, AAV7, AAV8, AAV9, AAV10, AAV11, AAV12, AAV-PHP.B, AAV-PHP.eB, and AAV-PHP.S. In some examples, AAV vectors containing, for example, multiple crRNAs, multiple sgRNAs, Cas9 coding sequences, dCas9 coding sequences, or MS2 transcription activator fusion protein coding sequences have tropism for specific tissues or cell types, for example, as shown below. [Table 3]

[0083] Cas9: RNA-guided DNA endonuclease enzyme involved in CRISPR-Cas immune defense against prokaryotic viruses. Cas9 has two active cleavage sites (HNH and RuvC), one on each strand of the double helix. An exemplary native Cas9 sequence from S. pyogenes is shown in SEQ ID NO:31.

[0084] The present disclosure also includes catalytically inactive (inactivated or dead) Cas9 (dCas9) that has reduced or eliminated endonuclease activity but still binds to dsDNA. In some examples, dCas9 includes one or more mutations in RuvC and HNH nuclease domains, such as one or more of the following point mutations: D10A, E762A, D839A, H840A, N854A, N863A, and D986A (e.g., based on the numbering of SEQ ID NO: 31). An exemplary dCas9 sequence with D10A and H840A substitutions is shown in SEQ ID NO: 33. In one example, dCas9 protein has mutations D10A, H840A, D839A, and N863A (see, e.g., Esvelt et al., Nat. Meth. 10:1116-21, 2013).

[0085] In some examples, Cas9 or dCas9 includes a transcription activation domain, such as VP64, P65, MyoD1, HSF1, RTA, SET7 / 9, or any combination thereof. In other examples, Cas9 or dCas9 does not include a transcription activation domain, such as VP64, P65, MyoD1, HSF1, RTA, SET7 / 9, or any combination thereof.

[0086] Cas9 sequences are publicly available. For example, GenBank® Accession Nos. CP012045.1, nucleotides 796693..800799 and CP014139.1, nucleotides 1100046..1104152 disclose Cas9 nucleic acids, and GenBank® Accession Nos. NP_269215.1, AMA70685.1, and AKP81606.1 disclose Cas9 proteins. In some examples, the Cas9 is an inactivated form of Cas9 (dCas9), such as one that is nuclease-deficient (e.g., one shown in GenBank® Accession Nos. AKA60242.1 and KR011748.1). An activatable Cas9 protein is provided in US Patent Application Publication No. 2018-0073002-A1.

[0087] In particular examples, the Cas9 or dCas9 used in the disclosed methods or kits has at least 80% sequence identity, e.g., at least 85%, at least 90%, at least 95%, at least 98%, or at least 99% sequence identity to such sequences (e.g., SEQ ID NOs: 31 and 33) and retains the ability to be used in the disclosed methods (e.g., can be used in an mTGA system to increase expression of a target gene).

[0088] Complementarity: The ability of a nucleic acid to form hydrogen bond(s) with another nucleic acid sequence, either by conventional Watson-Crick base pairing or other non-conventional methods. Percent complementarity indicates the percentage of residues in a nucleic acid molecule that can form hydrogen bonds (e.g., Watson-Crick base pairing) with a second nucleic acid sequence (e.g., 5, 6, 7, 8, 9 and 10 out of 10 are 50%, 60%, 70%, 80%, 90% and 100% complementary, respectively).

[0089] Control: Reference standard. In some embodiments, the control is a negative control sample obtained from a healthy subject. In other embodiments, the control is a positive control sample obtained from a subject diagnosed with a disease, for example, a disease associated with low expression of the target gene, such as muscular dystrophy. In still other embodiments, the control is a historical control or standard reference value or range of values ​​(e.g., a group of samples from subjects with known diagnosis and / or outcome, or a group of samples representing baseline or normal values).

[0090] The difference between the test sample and the control can be an increase or, conversely, a decrease. In some examples, the expression of the target gene increases compared to the control. The difference can be a qualitative difference or a quantitative difference, such as a statistically significant difference. In some examples, the difference is, for example, at least about 5%, for example, at least about 10%, at least about 20%, at least about 30%, at least about 40%, at least about 50%, at least about 60%, at least about 70%, at least about 80%, at least about 90%, at least about 100%, at least about 150%, at least about 200%, at least about 250%, at least about 300%, at least about 350%, at least about 400%, at least about 500%, or more than 500% increase compared to the control. In some examples, the difference is, for example, a reduction of at least about 5%, e.g., at least about 10%, at least about 20%, at least about 30%, at least about 40%, at least about 50%, at least about 60%, at least about 70%, at least about 80%, at least about 90%, at least about 95%, at least about 98%, at least about 99%, or 100% compared to the control.

[0091] CRISPR / Cas9 system: The CRISPR / Cas system is a prokaryotic immune system that confers resistance to foreign genetic elements such as plasmids and phages, providing a form of acquired immunity. CRISPR spacers recognize and cleave exogenous genetic elements in a manner similar to RNAi in eukaryotes. The CRISPR / Cas system can be used to regulate gene expression using the disclosed mTGA system, specifically, to activate expression by delivering dCas9 protein, dgRNA, or both, without cleaving double-stranded DNA (dsDNA). Activation of expression of target genes (or other nucleic acid molecules) can be achieved without cleaving dsDNA.

[0092] CRISPR RNA (crRNA): Part of the CRISPR / Cas9 system. The crRNA is an RNA molecule that hybridizes with the tracrRNA to form a unique dual RNA hybrid structure that binds to and guides the Cas9 endonuclease to the target sequence. In addition to the repeat sequence that hybridizes with the tracrRNA, the crisprRNA also contains a targeting sequence that has complementarity to the target gene. Similar to the dgRNA (described below), the crRNA can contain a truncated targeting sequence of about 14-15 base pairs, which allows the crRNA to guide wild-type Cas9 to the target sequence but does not induce double-stranded DNA breaks. In some examples, the crRNA is an RNA molecule (e.g., when expressed in a cell). In some examples, the crRNA is encoded by a DNA molecule (e.g., when in a vector, such as a viral vector).

[0093] Dead guide RNA (dgRNA): A truncated single-stranded guide RNA (sgRNA) that can guide Cas9 to a target sequence but does not induce double-stranded DNA cleavage. A truncated sgRNA contains a truncated targeting sequence of about 14-15 nucleotides, while a non-dead sgRNA contains a targeting sequence of about 20 nucleotides. dgRNAs are further described, for example, in Dahlman et al. (2015) Nat. Biotechnol. 33:1159-1161; Kiani et al. (2015) Nat. Methods, 12:1051-1054; and Hsin-Kai Liao et al. (2017) Cell, 171:1495-1507. In some examples, the dgRNA is an RNA molecule (e.g., when expressed in a cell). In some examples, the dgRNA is encoded by a DNA molecule (e.g., when in a vector, such as a viral vector).

[0094] Effective amount: A sufficient amount of an agent (e.g., multiplexed sgRNA, multiplexed crRNA or mTGA system provided herein) to produce a beneficial or desired result. The therapeutically effective amount may vary depending on one or more of the subject and disease state being treated, the subject's weight and age, the severity of the disease state, the mode of administration, etc., which can be easily determined by one of ordinary skill in the art. Beneficial therapeutic effects may include: feasibility of diagnostic determination; amelioration of a disease, symptom, disorder, or pathological condition; reduction or prevention of the onset of a disease, symptom, disorder, or pathological condition; and generally combating a disease, symptom, disorder, or pathological condition. An effective amount can be determined by varying the dosage and measuring the resulting response, such as expression of a target gene. An effective amount can also be determined by various in vitro, in vivo, or in situ assays.

[0095] In one embodiment, an "effective amount" is an amount sufficient to reduce a disease symptom by, for example, at least 10%, at least 20%, at least 30%, at least 40%, at least 50%, at least 60%, at least 70%, at least 90%, at least 95%, at least 99%, or 100% (compared to a suitable control, such as non-administration of a therapeutic agent). The term also applies to a dose that allows sufficient expression of Cas9 (or dCas9), multiple crRNAs, and / or multiple sgRNAs to allow targeting (e.g., alteration of expression) of a target gene.

[0096] Effective amount includes partial doses that contribute in combination with previous or subsequent administration to achieve effective response.For example, effective amount of drug can be administered in a single dose or in several doses, for example, hourly, daily, during the course of treatment that lasts for several days or weeks.However, effective amount can depend on the subject to be treated, the severity and type of the condition to be treated, and the mode of administration.The unit dosage form of drug can be packaged in a certain amount or in multiples of effective amount, for example, in vial (for example, with pierceable cap), tablet, or other form.

[0097] Fusion protein: A protein that includes at least a portion of the sequence of a full-length first protein (e.g., MS2) and at least a portion of the sequence of a full-length second protein (e.g., a transcription activator), where the first and second proteins are different. The two different peptides can be linked directly or indirectly, for example, using a linker (e.g., a linker of Gly, Ser, or combinations thereof, e.g., GGGGS). Exemplary fusion proteins include an MS2 domain (e.g., amino acids 1-130 of SEQ ID NO: 35) fused directly or indirectly to one or more transcription activation domains, such as one or more of VP64, p65, MyoD1, HSF1, RTA, or SET7 / 9, such as an MS2-P65-HSF1 fusion protein (e.g., SEQ ID NO: 35 and Konermann et al., Nature, 2015 Jan 29;517(7536):583-8).

[0098] Increase or decrease: A positive or negative change in amount from a reference value, respectively. An increase is a positive change, such as an increase of at least 25%, at least 50%, at least 75%, at least 100%, at least 200%, at least 300%, at least 400%, or at least 500% compared to the control value. For example, the increase can be about 25-500%, about 25-400%, about 25-300%, about 25-200%, about 25-100%, about 25-75%, about 25-50%, about 50-500%, about 75-500%, about 100-500%, about 200-500%, about 300-500%, about 400-500%, about 50-100%, about 50-200%, about 50-300%, about 50-400%, about 50-500%, about 100-200%, about 100-300%, about 100-400%, about 100-500%, or about 250-500%. A decrease is a negative change, such as a decrease of at least 20%, at least 25%, at least 50%, at least 75%, at least 80%, at least 90%, at least 95%, at least 98%, at least 99%, or at least 100% compared to a control value. For example, the reduction can be about 25-100%, about 25-98%, about 25-95%, about 25-90%, about 25-80%, about 25-75%, about 25-50%, about 50-100%, about 75-100%, about 90-100%, about 95-100%, about 98-100%, about 99-100%, about 50-75%, about 50-80%, about 50-90%, about 50-95%, about 50-98%, about 75-80%, about 75-90%, about 75-95%, or about 75-98%.

[0099] Inhibiting or Treating a Disease: "Treatment" refers to a therapeutic intervention that improves the signs or symptoms of a disease or pathological condition after infection when the disease begins to develop. The term "ameliorating" in relation to a disease or pathological condition refers to an observable beneficial effect of treatment. Inhibiting a disease can include alleviating the symptoms of a disease. A beneficial effect can be evidenced, for example, by a delay in the onset of clinical symptoms of the disease in a subject, a reduction in the severity of some or all clinical symptoms of the disease, a slower progression of the disease, an increase in the expression of a target gene, an improvement in the overall health or well-being of the subject, or other parameters specific to a particular disease.

[0100] A "prophylactic" treatment is a treatment administered to a subject who shows no signs of disease or who shows only early signs, for the purpose of reducing the risk of developing a pathological condition. In some embodiments, the disclosed methods are therapeutic, and not prophylactic.

[0101] Isolated: An "isolated" biological component (e.g., a protein, nucleic acid, or cell) is substantially separated from, produced separately from, or purified from other biological components, such as other cells, chromosomal and extrachromosomal DNA and RNA, and proteins, in the cells or tissues of the organism in which it is present. "Isolated" nucleic acids and proteins include nucleic acids and proteins purified by standard purification methods. The term also encompasses nucleic acids and proteins prepared by recombinant expression in a host cell, as well as chemically synthesized nucleic acids and proteins. For example, an isolated vector comprising a nucleic acid encoding the disclosed multiple crRNAs, multiple sgRNAs, or proteins (e.g., dCas9, Cas9, or MS2 transcription activator fusion proteins), or a cell comprising such a vector, is in some instances at least 50% pure, e.g., at least 75%, at least 80%, at least 90%, at least 95%, at least 98%, at least 99%, or 100% pure.

[0102] Label: A compound or composition that is directly or indirectly conjugated to another molecule (such as a nucleic acid molecule) to facilitate detection of the molecule. Specific non-limiting examples of labels include fluorescent and fluorogenic moieties, chromogenic moieties, haptens, affinity tags, and radioisotopes. Labels can be directly detectable (e.g., optically detectable) or indirectly detectable (e.g., through interaction with one or more additional molecules that can then be detected).

[0103] Liver disease: acute or chronic damage of the liver. In some examples, liver disease is treated with liver transplantation. Examples of liver diseases that can be treated with the disclosed methods and compositions include, but are not limited to, hepatitis (such as hepatitis A, B or C), liver fibrosis, liver cirrhosis, alcoholic liver disease, hepatocellular carcinoma, Alagille syndrome, alpha-1 antitrypsin deficiency (alpha-1), biliary atresia, galactosemia, Gilbert syndrome, hemochromatosis, lysosomal acid lipase deficiency (LAL-D), non-alcoholic fatty liver disease (NAFLD), primary biliary cholangitis (PBC), primary sclerosing cholangitis (PSC), glycogen storage disease type I (GSD I), blood clotting factor deficiency (e.g., factor I, factor II, factor V, factor V+VIII, factor VII, factor X, factor XI or factor XIII is missing or does not function properly) and Wilson's disease.

[0104] Male-specific bacteriophage 2 (MS2): An RNA virus that contains an RNA operator hairpin that binds to a coat protein (i.e., an MS2 domain or MS2 protein; e.g., amino acids 1-130 of SEQ ID NO:35). The MS2 binding loop (i.e., an MS2 hairpin or MS2 stem loop; e.g., SEQ ID NO:16) and the MS2 protein are incorporated into the synergistic activation mediator (SAM) complex in the second generation CRISPR-Cas9 system. Such modifications of the MS2 hairpin sequence can be incorporated into sgRNAs, e.g., dgRNAs, or as provided herein to modify tracrRNAs (e.g., SEQ ID NOs:17-19). The MS2 protein (e.g., amino acids 1-130 of SEQ ID NO:35) can be incorporated into fusion proteins to recruit transcription factors.

[0105] Operably linked: A first nucleic acid sequence is operably linked to a second nucleic acid sequence when the first nucleic acid sequence is in a functional relationship with the second nucleic acid sequence. For example, a promoter is operably linked to a coding sequence (such as the coding sequence of a crRNA, sgRNA, dCas9, Cas9, or MS2 transcription activator fusion protein) when the promoter affects the transcription or expression of the coding sequence. Generally, operably linked DNA sequences are contiguous and, where necessary to link two protein coding regions, are in the same reading frame.

[0106] Pharmaceutically acceptable carriers: Pharmaceutically acceptable carriers useful in the present invention are conventional. Remington's Pharmaceutical Sciences, by E. W. Martin, Mack Publishing Co., Easton, PA, 15th Edition (1975) describes compositions and formulations suitable for pharmaceutical delivery of the disclosed compositions provided herein (e.g., multiple crRNAs, multiple sgRNAs, RNA, vectors, RNP complexes, mTGA systems).

[0107] Generally, the nature of the carrier depends on the particular mode of administration used.For example, parenteral formulations usually contain injectable fluids that contain pharma- ceutical and physiologically acceptable fluids such as water, physiological saline, balanced salt solutions, aqueous dextrose, glycerol, etc. as vehicles.In addition to biologically neutral carriers, the pharmaceutical compositions to be administered can contain small amounts of non-toxic auxiliary substances, such as wetting agents or emulsifiers, preservatives and pH buffering agents, for example, sodium acetate or sorbitan monolaurate.

[0108] Promoter: A group of nucleic acid control sequences that direct the transcription of a nucleic acid. A promoter contains necessary nucleic acid sequences near the start site of transcription. A promoter also contains distal enhancer or repressor elements, as appropriate. A "constitutive promoter" is a promoter that is continuously active and is not subject to regulation by external signals or molecules. In contrast, the activity of an "inducible promoter" is regulated by an external signal or molecule (e.g., a transcription factor). In some examples, the vectors provided herein contain pol III promoters (e.g., U6 and H1 promoters), pol II promoters (e.g., retroviral Rous sarcoma virus (RSV) LTR promoter (optionally with an RSV enhancer), cytomegalovirus (CMV) promoter (optionally with a CMV enhancer), SV40 promoter, Spc5.12 promoter, CW3SL promoter, dihydrofolate reductase promoter, β-actin promoter, phosphoglycerol kinase (PGK) promoter and EF1α promoter), or combinations thereof.

[0109] Recombinant cell or host cell: A cell that has been genetically modified or can be genetically modified by the introduction of an exogenous polynucleotide, such as a recombinant plasmid or vector. Typically, a host cell is a cell that can propagate a vector and express its nucleic acid. Such cells can be eukaryotic or prokaryotic. This term also includes any progeny of the subject host cell. It is understood that all progeny may not be identical to the parent cell, since there may be mutations that occur during replication. However, such progeny are included when the term "host cell" is used.

[0110] Regulatory element: a phrase including promoters, enhancers, internal ribosome entry sites (IRES) and other expression control elements (e.g., transcription termination signals such as polyadenylation signals and polyU sequences). Such regulatory elements are described, for example, in Goeddel, Gene Expression Technology: Methods In Enzymology 185, Academic Press, San Diego, Calif. (1990). Regulatory elements include those that direct constitutive expression of a nucleotide sequence in many types of host cells and those that direct expression of a nucleotide sequence only in certain host cells (e.g., tissue-specific regulatory sequences). Tissue-specific promoters may direct expression primarily in a desired tissue of interest, such as muscle, neurons, bone, skin, blood, a specific organ (e.g., liver, pancreas), or a specific cell type (e.g., muscle or liver cells). Regulatory elements may also direct expression in a time-dependent manner, for example, in a cell cycle-dependent or developmental stage-dependent manner, which may or may not also be tissue or cell type specific.

[0111] The term "regulatory element" also encompasses enhancer elements such as the WPRE; the CMV enhancer; the R-U5' segment in the LTR of HTLV-I; the SV40 enhancer; and the intron sequence between exon 2 and exon 3 of rabbit β-globin.

[0112] Reporter protein: any protein whose expression is related to the expression of gene of interest. Exemplary reporter proteins include fluorescent proteins and chemiluminescent molecules, such as infrared fluorescent protein (IFP), mRFP1, mCherry, mOrange, DsRed, tdTomato, mKO, tagRFP, EGFP, mEGFP, mOrange2, maple, tagRFP-T, firefly luciferase, Renilla luciferase and click beetle luciferase (e.g., US Patent Application Publication No. 2010 / 0122355). In some examples, reporter protein is placed downstream of gene of interest and in frame with gene of interest, so that reporter protein is co-expressed with gene of interest.

[0113] Single guide RNA (sgRNA): A polynucleotide sequence used to guide Cas9 or dCas9 protein to a target nucleic acid sequence. In the endogenous Cas9 system, the trans-activating crRNA (tracrRNA) is an RNA molecule that hybridizes with a repeat sequence of another RNA molecule known as CRISPR RNA (crRNA) to form a unique dual RNA hybrid structure that binds to and guides the Cas9 endonuclease to the target sequence. The crRNA contains a targeting sequence complementary to the target gene, thus facilitating the binding of the Cas9 complex to the target sequence.

[0114] sgRNA is a synthetic chimera that combines crRNA and tracrRNA into a single RNA transcript. The use of sgRNA simplifies the system while retaining fully functional Cas9-mediated sequence-specific targeting. Changing the targeting sequence within the crRNA portion of the sgRNA allows for targeting of any DNA or RNA sequence of interest. (See CRISPR-Cas9 Structures and Mechanisms. Fuguo Jiang and Jennifer A. Doudna, Annual Review of Biophysics, 46:1, 505-529 (2017)).

[0115] In some examples, the sgRNA is an RNA molecule (e.g., when expressed in a cell). In some examples, the sgRNA is encoded by a DNA molecule (e.g., when in a vector, such as a viral vector). The sgRNA nucleic acid can include modified bases or chemical modifications (see, e.g., Latorre et al., Angewandte Chemie 55:3548-50, 2016). In some examples, the sgRNA includes two or more MS2-binding loop sequences that can be modified from the native MS2-binding loop sequence to increase the GC content and / or shorten the repetitive content. In some examples, the sgRNA is modified to increase the GC content and / or shorten the repetitive content. In some examples, the sgRNA is a dead guide RNA (dgRNA). Increasing the GC content and / or shortening the repetitive content of the sgRNA can be used to convert the sgRNA into a dgRNA, i.e., a guide nucleic acid molecule that can guide the Cas9 or dCas9 protein to a target sequence but does not induce DNA double-strand breaks.

[0116] Sequence identity / similarity: The similarity between amino acid (or nucleotide) sequences is expressed in terms of the similarity between the sequences, otherwise referred to as sequence identity. Sequence identity is frequently measured in terms of identity (or similarity or homology) percentage. The higher the percentage, the more similar the two sequences are.

[0117] Methods for aligning sequences for comparison are described.Various programs and alignment algorithms are described in Smith and Waterman, Adv. Appl. Math. 2:482, 1981; Needleman and Wunsch, J. Mol. Biol. 48:443, 1970; Pearson and Lipman, Proc. Natl. Acad. Sci. USA 85:2444, 1988; Higgins and Sharp, Gene 73:237, 1988; Higgins and Sharp, CABIOS 5:151, 1989; Corpet et al., Nucleic Acids Research 16:10881, 1988; and Pearson and Lipman, Proc. Natl. Acad. Sci. USA 85:2444, 1988. Altschul et al., Nature Genet. 6:119, 1994, presents a detailed discussion of sequence alignment methods and homology calculations.

[0118] The NCBI Basic Local Alignment Search Tool (BLAST) (Altschul et al., J. Mol. Biol. 215:403, 1990) is available from several sources, including the National Center for Biotechnology Information (NCBI, Bethesda, MD) and on the Internet, for use in conjunction with the sequence analysis programs blastp, blastn, blastx, tblastn, and tblastx. Instructions on how to use this program to determine sequence identity are available on the Internet at the NCBI website.

[0119] Variants of known protein and nucleic acid sequences and those disclosed herein are typically characterized as having at least about 80%, at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity counted over a full length alignment with an amino acid sequence using NCBI Blast set to default parameters. When less than the entire sequence is compared for sequence identity, homologs and variants typically have at least 80% sequence identity over a short window of 10-20 amino acids, and may have at least 85% or at least 90% or at least 95% sequence identity depending on their similarity to the reference sequence. Methods for determining sequence identity over such short windows are available on the Internet at the NCBI website.

[0120] In one example, the nucleic acid encoding the multiple crRNA or multiple sgRNA has at least 80%, at least 85%, at least 90%, at least 91%, at least 92%, at least 93%, at least 94%, at least 95%, at least 96%, at least 97%, at least 98%, or at least 99% sequence identity to SEQ ID NO:1, 2, 3, 4, 5, 6, 53, 54, or 55.

[0121] Subject: a vertebrate, such as a human or non-human mammal. Mammals include, but are not limited to, mice, monkeys, humans, farm animals, sports animals, and pets. In one embodiment, the subject is a non-human mammalian subject, such as a monkey or other non-human primate, mouse, rat, rabbit, pig, goat, sheep, dog, cat, horse, or cow. In some examples, the subject is a human. In some examples, the subject has a disorder or genetic disease that can be treated using the methods provided herein, such as a disorder resulting from reduced gene expression. In some examples, the subject is an experimental animal / organism, such as a zebrafish, Xenopus, C. elegans, Drosophila, mouse, rabbit, rat, or primate.

[0122] Target gene (or "target"): a gene (or group of genes) for which increased or decreased expression of a gene product (e.g., a protein) is desired, e.g., a gene for which activated expression is desired. A gene can be targeted directly or indirectly, as long as it affects the expression of the target gene. In some examples, a targeting sequence (such as a crRNA or sgRNA targeting sequence) has complementarity to the target gene. In some examples, a targeting sequence has complementarity to the promoter and / or regulatory elements of the target gene.

[0123] Targeting sequence: A portion of a crRNA or sgRNA that has complementarity to a target nucleic acid sequence. In some examples, the targeting sequence has complementarity to a promoter or regulatory element of a target gene for which activated expression is desired. In some examples, the targeting sequence is about 14-30 nt and has sufficient complementarity with the target nucleic acid sequence to hybridize with the target sequence and direct sequence-specific binding of Cas9 or dCas9 to the target nucleic acid sequence. In some embodiments, the degree of complementarity between a targeting sequence and its corresponding target sequence is about 50%, 60%, 75%, 80%, 85%, 90%, 95%, 97.5%, 98%, 99% or 100% or more when optimally aligned using a suitable alignment algorithm. In some embodiments, the degree of complementarity is 100%. Optimal alignment may be determined using any suitable algorithm for aligning sequences, non-limiting examples of which include the Smith-Waterman algorithm, the Needleman-Wunsch algorithm, algorithms based on the Burrows-Wheeler transformation (e.g., Burrows Wheeler Aligner), ClustalW, Clustal X, BLAT, Novoalign (Novocraft Technologies, ELAND (Illumina, San Diego, Calif.), SOAP (available at soap.genomics.org.cn) and Maq (available at maq.sourceforge.net).

[0124] Therapeutic Agent: refers to one or more molecules or compounds that provide some beneficial effect upon administration to a subject. Beneficial therapeutic effects can include enabling a diagnostic determination; ameliorating a disease, symptom, disorder, or pathological condition; reducing or preventing the onset of a disease, symptom, disorder, or pathological condition; and generally combating a disease, symptom, disorder, or pathological condition.

[0125] Transcriptional activator: A protein or protein domain that increases the transcription of a nucleic acid molecule, such as a gene. Such proteins can be used in the methods and mTGA systems provided herein, for example, to assist in the recruitment of cofactors and RNA polymerase for the transcription of a target gene. Such proteins and protein domains can have a DNA binding domain and a domain for transcriptional activation. These activators can be introduced into the system by binding to Cas9, dCas9, sgRNA, tracrRNA or crRNA. Examples of such activators include VP64, p65, myogenic differentiation 1 (MyoD1), heat shock transcription factor (HSF) 1, RTA, SET7 / 9 or any combination thereof, such as p65 and HSF1.

[0126] Transactivating crRNA (tracrRNA): An RNA molecule that hybridizes with a repeat sequence of another RNA molecule known as CRISPR RNA (crRNA) to form a unique dual RNA hybrid structure that binds and guides Cas9 endonuclease to a target sequence. Disclosed herein are modified tracrRNAs that contain two or more MS2-binding loop sequences that have been modified from the native MS2-binding loop sequence to increase GC content and / or shorten repetitive content. In some examples, the MS2-binding loop sequence promotes binding by an MS2 transcription activator fusion protein. In some examples, the tracrRNA is an RNA molecule (e.g., when expressed in a cell). In other examples, the tracrRNA is encoded by a DNA molecule (e.g., when in a vector such as a viral vector).

[0127] Transduction, transformation and transfect: A virus or vector "transduces" a cell when it transfers a nucleic acid molecule to the cell. A cell is "transformed" or "transfected" by a nucleic acid introduced into the cell when the nucleic acid is stably replicated by the cell, either by integration of the nucleic acid into the cell genome or by episomal replication.

[0128] These terms encompass all techniques that can introduce nucleic acid molecules into such cells, including transfection with viral vectors, transformation with plasmid vectors, and introduction of naked DNA by electroporation, lipofection, particle gun acceleration, and other methods in the art. In some examples, the methods are chemical methods (e.g., calcium phosphate transfection), physical methods (e.g., electroporation, microinjection, or particle bombardment), fusion (e.g., liposomes), receptor-mediated endocytosis (e.g., DNA-protein complexes or viral envelope / capsid-DNA complexes), and biological infection with viruses, such as recombinant viruses (Wolff, JA, ed, Gene Therapeutics, Birkhauser, Boston, USA, 1994). Methods for introducing nucleic acid molecules into cells are known (see, e.g., U.S. Pat. No. 6,110,743). These methods can be used to transduce cells with the disclosed agents to activate expression.

[0129] Transgene: An exogenous gene.

[0130] Vector: A nucleic acid molecule into which a foreign nucleic acid molecule can be introduced without destroying the vector's ability to replicate and / or integrate in a host cell. Vectors include, but are not limited to, single-stranded, double-stranded, or partially double-stranded nucleic acid molecules; nucleic acid molecules that contain one or more free ends or no free ends (e.g., circular); nucleic acid molecules that contain DNA, RNA, or both; and various other polynucleotides (e.g., LNA).

[0131] A vector can contain a nucleic acid sequence that allows replication in a host cell, such as an origin of replication. A vector can also contain one or more selectable marker genes and other genetic elements. An integrating vector can integrate itself into a host nucleic acid. An expression vector is a vector that contains the necessary regulatory sequences to allow transcription and translation of the inserted gene or genes.

[0132] One type of vector is a "plasmid", which refers to a circular double-stranded DNA loop into which additional DNA segments can be inserted, such as by standard molecular cloning techniques. Another type of vector is a viral vector, in which a DNA or RNA sequence derived from a virus is present in the vector for packaging into a virus (e.g., retrovirus, replication-defective retrovirus, adenovirus, replication-defective adenovirus, and adeno-associated virus). A viral vector also includes a polynucleotide carried by the virus for transfection into a host cell. In some embodiments, the vector is a lentivirus (such as an integration-defective lentivirus vector) or an adeno-associated virus (AAV) vector.

[0133] Certain vectors are capable of autonomous replication in a host cell into which they are introduced (e.g., bacterial vectors having a bacterial origin of replication and episomal mammalian vectors), while other vectors (e.g., non-episomal mammalian vectors) are integrated into the genome of a host cell upon introduction into the host cell, and thereby are replicated along with the host genome.

[0134] Certain vectors can direct the expression of genes to which they are operably linked. Such vectors are referred to herein as "expression vectors". Common expression vectors are often in the form of plasmids. A recombinant expression vector can contain the nucleic acids provided herein (e.g., nucleic acids encoding multiple crRNAs, multiple sgRNAs, or proteins such as Cas9, dCas9, or MS2 transcription activator fusion proteins, etc.) in a form suitable for expression of the nucleic acid in a host cell, meaning that the recombinant expression vector contains one or more regulatory elements operably linked to the nucleic acid sequence to be expressed, which may be selected based on the host cell used for expression. Within a recombinant expression vector, "operably linked" is intended to mean that the nucleotide sequence of interest is linked to the regulatory element(s) in a manner that allows expression of the nucleotide sequence (e.g., in an in vitro transcription / translation system or in a host cell when the vector is introduced into the host cell). It will be understood by those skilled in the art that the design of the expression vector may depend on factors such as the choice of the host cell to be transformed, the desired expression level, etc. The vectors can be introduced into host cells to thereby produce transcripts, proteins or peptides, including fusion proteins or peptides, encoded by the nucleic acids described herein.

[0135] II. Overview of Some Embodiments Duchenne muscular dystrophy (DMD) is caused by early mutations in the cytoplasmic protein dystrophin, leading to progressive muscle degeneration and weakness. A potential treatment strategy is the activation of the utrophin (Utrn) gene (>10 kbp), a homolog of dystrophin. However, traditional transgene methods cannot efficiently introduce utrophin into mature muscle due to large gene size and limited AAV capacity. Similar limitations affect the ability to treat other genetic diseases (e.g., see Tables 1 and 2 below).

[0136] The CRISPR / Cas9 targeted gene activation (TGA) system utilizes modified CRISPR / Cas9 machinery and co-transcriptional complexes to 1) rescue levels of gene expression (e.g., restore Klotho levels after acute kidney injury or in mdx models), 2) compensate for genetic defects (e.g., overexpress utrophin to compensate for loss of dystrophin), and 3) alter cell fate by inducing transdifferentiation factors (e.g., generate insulin-producing cells by ectopically expressing Pdx1) (see U.S. Patent Application No. 17 / 104,372, incorporated herein by reference in its entirety). Conventional transgene methods are limited by vector capacity, so the TGA system is unmatched in its ability to activate genes larger than 8 kbp. The CRISPR / Cas9-based TGA system uses modified tracrRNA, sgRNA, or dgRNA containing Cas9 and MS2-binding aptamer loops to recruit MS2-p65-HSF1 (MPH) fusion proteins to gRNA binding sites in gene promoters for gene activation without cleaving the genome. Previous studies have shown that the TGA system can induce endogenous expression of utrophin, but the activation level is mild (Liao et al. (2017) Cell, 171(7):1495-1507).

[0137] Disclosed herein is a multiplex target gene activation (mTGA) system that multiplexes CRISPR RNA (crRNA) and / or modified single guide RNA (sgRNA) to synergistically activate gene expression. In the examples, it is shown that simultaneous delivery of multiple crRNAs and / or sgRNAs enhances utrophin activation without the need to increase the total RNA concentration. Although several examples are provided in relation to utrophin activation and treatment of DMD, the system can be used to activate any other target gene or to treat other diseases in which target gene activation is desired.

[0138] III. Multiplex crRNA and multiplex sgRNA With reference to Figures 1-4, provided herein are nucleic acid molecules encoding multiple CRISPR RNAs (crRNAs) 100 and multiple single guide RNAs (sgRNAs) 200. One of skill in the art will recognize that the crRNAs and sgRNAs, when present in a vector (e.g., AAV vector), are encoded by DNA, and that "T" is replaced with "U" when expressed in a cell and transcribed as RNA. Thus, certain SEQ ID NOs herein show "T" for a crRNA, sgRNA, or portion thereof, but when expressed as RNA, "T" becomes "U". Additionally, Figures 1-4 show coding sequences (e.g., DNA) where a promoter (e.g., 110, 111, 112, 113) is shown, but the corresponding encoded RNA will not include a promoter sequence. Thus, in some examples, 100 and 200 are RNA molecules that do not include promoters 110, 111, 112, 113.

[0139] As shown in Figure 1, in some embodiments, the nucleic acid molecule encoding the multiple crRNA 100 encodes multiple crRNAs, such as two crRNAs (e.g., Figure 1), three crRNAs (e.g., Figures 2A-2B) or more. In some examples, the nucleic acid molecule encoding the multiple crRNA 100 includes, from 5' to 3', a first promoter 110, a nucleic acid molecule encoding a modified trans-activating CRISPR RNA (tracrRNA) 130, a first cleavage site 120, a first nucleic acid molecule encoding a first crRNA 101, a second cleavage site 121, and a second nucleic acid molecule encoding a second crRNA 102.

[0140] As shown in Figures 2A-2B, in some embodiments, the nucleic acid molecule encoding the multiple crRNA 100 further comprises a third nucleic acid molecule 103 encoding a third crRNA or modified single guide RNA (sgRNA) operably linked to a second promoter 111. In some examples, the second promoter 111 and the third nucleic acid molecule 103 are in a forward orientation and are located either i) 3' of the second nucleic acid molecule encoding the second crRNA 102 (e.g., Figure 2A) or ii) 5' of the first promoter (not shown). In other examples, the second promoter 111 and the third nucleic acid molecule 103 are in a reverse orientation and are located 5' of the first promoter 110 (e.g., Figure 2B). Whether the second promoter 111 and the third nucleic acid molecule 103 are in a "reverse orientation" is determined with respect to the orientation of the first promoter 110. Thus, when the second promoter 111 and the third nucleic acid 103 are in "reverse orientation," it means that the sequences of the second promoter and the third nucleic acid are read in the opposite direction to that of the first promoter 111 (e.g., Figure 2B).

[0141] Since the gene targets are selected independently, in some examples, the first nucleic acid molecule encoding the first crRNA101 and the second nucleic acid molecule encoding the second crRNA102 target different genes, for example, the first crRNA can target utrophin and the second crRNA can target EEF1α2, Fst, Pdx1, Klotho, Interleukin 10, or Six2. In other examples, the second crRNA targets utrophin and the first crRNA targets EEF1α2, Fst, Pdx1, Klotho, Interleukin 10, or Six2. In a specific, non-limiting example, the first crRNA101 targets utrophin and the second crRNA102 targets EEF1a2.

[0142] In some embodiments, the first and second crRNA101, 102 target the same gene, such as both targeting utrophin. The first and second crRNA101, 102 can target the same gene using the same targeting sequence. For example, the first crRNA101 and the second crRNA102 can both consist of SEQ ID NO:8 or SEQ ID NO:9. The first crRNA101 and the second crRNA102 can also target the same gene using different targeting sequences, for example, the first crRNA101 can consist of SEQ ID NO:8 and the second crRNA102 can consist of SEQ ID NO:9.

[0143] In some examples, the first nucleic acid molecule encoding the first crRNA101 or the second nucleic acid molecule encoding the second crRNA102 has at least 70%, at least 80%, at least 85%, at least 90%, at least 95%, at least 98%, at least 99%, or 100% sequence identity with, or consists of, SEQ ID NO:8 or SEQ ID NO:9, 49, 50, 51, or 52. In some examples, the first nucleic acid molecule encoding the first crRNA101 has at least 95% sequence identity with, or consists of, SEQ ID NO:8 or SEQ ID NO:51. In further examples, the second nucleic acid molecule encoding the second crRNA102 has at least 95% sequence identity with, or consists of, SEQ ID NO:9 or SEQ ID NO:52.

[0144] In some examples, the third nucleic acid molecule 103 encodes a modified single guide RNA (sgRNA). The modified sgRNA encodes at least one modified MS2 binding loop sequence. In some examples, the sgRNA encodes two or more modified MS2 binding loop sequences. In some examples, the modified sgRNA is a dgRNA.

[0145] In some examples, the modified sgRNA includes a targeting sequence that targets the same gene or sequence as the first crRNA101, the second crRNA102, or both. In some examples, the modified sgRNA includes a targeting sequence that targets a different gene or sequence than the first crRNA101, the second crRNA102, or both. In a specific, non-limiting example, the first crRNA101, the second crRNA102, and the modified sgRNA103 all target the same gene, such as utrophin. In some examples, the modified sgRNA targets the same gene as the first crRNA101, the second crRNA102, or both, but includes a targeting sequence that is different from the first crRNA101, the second crRNA102, or both (e.g., SEQ ID NO: 2). In a further example, the first crRNA101, the second crRNA102, and the modified sgRNA all target different genes or sequences, for example, the targets of the first crRNA101, the second crRNA102, and the modified sgRNA can be utrophin, EEF1α2, and Fst, respectively. In another non-limiting example, the targets of the first crRNA101, the second crRNA102, and the modified sgRNA can be utrophin, EEF1a2, and Klotho, respectively.

[0146] In some examples, the third nucleic acid molecule 103 encoding the modified sgRNA has at least 70%, at least 80%, at least 85%, at least 90%, at least 95%, at least 98%, at least 99%, or 100% sequence identity to SEQ ID NO: 10, 11, 12, 13, 14, 15, 42, 43, 44, 45, 46, 47, or 48. In some examples, the third nucleic acid molecule 103 encoding the modified sgRNA has at least 95% sequence identity to SEQ ID NO: 10, 11, 12, 13, 14, 15, 42, 43, 44, 45, 46, 47, or 48. In certain non-limiting examples, the third nucleic acid molecule 103 encoding the modified sgRNA comprises or consists of SEQ ID NO: 10, 11, 12, 13, 14, 15, 42, 43, 44, 45, 46, 47, or 48. In another specific, non-limiting example, the third nucleic acid molecule encoding the modified sgRNA103 has at least 95% sequence identity to, or comprises, or consists of, SEQ ID NO:12.

[0147] In a particular non-limiting example, the first nucleic acid molecule encoding the first crRNA101 has 90% sequence identity to SEQ ID NO:8, the second nucleic acid molecule encoding the second crRNA102 has 90% sequence identity to SEQ ID NO:9, and the third nucleic acid molecule encoding the modified sgRNA 103 has 90% sequence identity to SEQ ID NO:12. In another non-limiting example, the first nucleic acid molecule encoding the first crRNA101 comprises or consists of SEQ ID NO:8, the second nucleic acid molecule encoding the second crRNA102 comprises or consists of SEQ ID NO:9, and the third nucleic acid molecule encoding the modified sgRNA 103 comprises or consists of SEQ ID NO:12. In a further non-limiting example, the first nucleic acid molecule encoding the first crRNA101 has 90% sequence identity to SEQ ID NO:51, and the second nucleic acid molecule encoding the second crRNA102 has 90% sequence identity to SEQ ID NO:52. In another example, the first nucleic acid molecule encoding the first crRNA101 comprises or consists of SEQ ID NO:51, and the second nucleic acid molecule encoding the second crRNA102 comprises or consists of SEQ ID NO:52.

[0148] In some examples, the third nucleic acid molecule 103 encodes a third crRNA. In some examples, the third crRNA includes a targeting sequence that targets the same gene or sequence as the first crRNA, the second crRNA, or both. In some examples, the third crRNA includes a targeting sequence that targets a different gene or sequence than the first crRNA, the second crRNA, or both. In certain non-limiting examples, the first, second and third crRNAs all target the same gene or sequence, for example, all target utrophin. In some examples, the third crRNA targets the same gene as the first crRNA, the second crRNA, or both, but includes a targeting sequence that is different from the first crRNA, the second crRNA, or both. In a specific, non-limiting example, the first and second crRNA target the same gene or sequence, such as utrophin, and the third crRNA targets a different gene or sequence than the first and second crRNA, such as targeting Fst1 or EEF1α2.

[0149] In some examples, the third nucleic acid molecule encoding the third crRNA103 comprises at least 70%, at least 80%, at least 85%, at least 90%, at least 95%, at least 98%, at least 99%, or 100% sequence identity with SEQ ID NO: 8, 9, 51 or 52. In a particular non-limiting example, the third nucleic acid molecule encoding the third crRNA103 has at least 95% sequence identity with SEQ ID NO: 8, 9, 51 or 52. In another non-limiting example, the third nucleic acid molecule encoding the third crRNA103 consists of or comprises SEQ ID NO: 8, 9, 51 or 52.

[0150] The nucleic acid molecule encoding the modified tracrRNA130 further encodes at least one modified MS2 binding loop. In some examples, the modified tracrRNA encodes at least two modified MS2 binding loops. In some examples, the modified tracrRNA comprises one or more of SEQ ID NO: 17, 18, or 19. In certain non-limiting examples, the nucleic acid molecule encoding the modified tracrRNA130 comprises at least 70%, at least 80%, at least 85%, at least 90%, at least 95%, at least 98%, at least 99%, or 100% sequence identity with SEQ ID NO: 7. In certain non-limiting examples, the nucleic acid molecule encoding the modified tracrRNA103 comprises at least 95% sequence identity with SEQ ID NO: 7. In other non-limiting examples, the nucleic acid molecule encoding the modified tracrRNA130 comprises or consists of SEQ ID NO: 7.

[0151] In some examples, the nucleic acid molecule encoding the multiple crRNA100 comprises at least 70%, at least 80%, at least 85%, at least 90%, at least 95%, at least 98%, at least 99%, or 100% sequence identity with SEQ ID NO:1. In particular examples, the nucleic acid molecule encoding the multiple crRNA100 has at least 95% sequence identity with SEQ ID NO:1. In further examples, the nucleic acid molecule encoding the multiple crRNA100 comprises or consists of SEQ ID NO:1. In some examples, the nucleic acid molecule encoding the multiple crRNA100 has at least 70%, at least 80%, at least 85%, at least 90%, at least 95%, at least 98%, at least 99%, or 100% sequence identity with SEQ ID NO:2. In particular examples, the nucleic acid molecule encoding the multiple crRNA100 has at least 95% sequence identity with SEQ ID NO:2. In further examples, the nucleic acid molecule encoding the multiple crRNA100 comprises or consists of SEQ ID NO:2.

[0152] Also described herein are nucleic acid molecules encoding multiple sgRNA 200 containing two or more modified sgRNAs, as shown in Figures 3-4. The modified sgRNA encodes at least one modified MS2 binding loop sequence. In some examples, the modified sgRNA encodes two or more modified MS2 binding loop sequences. In some examples, the modified sgRNA comprises one or more of SEQ ID NO: 17, 18, or 19. In some examples, the modified sgRNA is a dgRNA.

[0153] In some embodiments, the nucleic acid encoding the multiple sgRNA 200 encodes two modified sgRNAs (e.g., FIG. 3A, FIG. 3C, and FIG. 3D). In some examples, the nucleic acid encoding the multiple sgRNA 200 includes, from 5' to 3', a first nucleic acid molecule encoding a first modified sgRNA 201 in a reverse orientation operably linked to a first promoter 112, and a second nucleic acid molecule encoding a second modified sgRNA 202 in a forward orientation operably linked to a second promoter 113 (see, e.g., FIG. 3A). Whether the first promoter 112 and the first modified sgRNA 201 are in a "reverse orientation" is determined with respect to the orientation of the second promoter 113. Thus, when the first promoter 112 and the first modified sgRNA 201 are in a "reverse orientation", it means that the sequence is read in the opposite direction to the direction of the second promoter 113 (e.g., FIG. 3A, FIG. 3B, FIG. 3E, and FIG. 4). In some examples, the nucleic acid encoding the multiple sgRNA 200 includes a first promoter 112 operably linked 5' to 3' to a first nucleic acid molecule encoding a first modified sgRNA 201, a cleavage site 122, and a second nucleic acid molecule 202 (see, e.g., FIG. 3C). In some examples, the nucleic acid encoding the multiple sgRNA 200 includes a first promoter 112 operably linked 5' to 3' to a first nucleic acid molecule encoding a first modified sgRNA 201, and a second promoter 113 operably linked to a second nucleic acid molecule 202 (see, e.g., FIG. 3D).

[0154] In some embodiments, the nucleic acid encoding the multiplex sgRNA 200 encodes three modified sgRNAs (e.g., Figures 3B and 3E). The third modified sgRNA 203 is separated from either the first modified sgRNA 201 or the second modified sgRNA 202 by the first cleavage site 122. When the third modified sgRNA 203 is located 3' of the second modified sgRNA 202, the first cleavage site 122 and the third modified sgRNA 203 are in a forward orientation (i.e., the same orientation as the second promoter 113) and are operably linked to the second promoter 113 (see, e.g., Figure 3B). Alternatively, the third nucleic acid molecule may be located 5' of the first modified sgRNA 201 (see, e.g., Figure 3E). When the third nucleic acid is 5' of the first modified sgRNA 201, the first cleavage site 122 and the third modified sgRNA 203 are encoded in the reverse orientation (i.e., the same orientation as the first promoter 112) and are operably linked to the first promoter 112.

[0155] In a further example, the nucleic acid encoding the multiplex sgRNA 200 comprises four modified sgRNAs (e.g., FIG. 4). When the multiplex sgRNA 200 comprises four modified sgRNA coding sequences, the third nucleic acid molecule is located 3' of the second modified sgRNA 202 and encodes the first cleavage site 122 and the third modified sgRNA 203 in a forward orientation (i.e., the same orientation as the second promoter 113) and is operably linked to the second promoter 113. The fourth nucleic acid is located 5' of the first modified sgRNA 201 and encodes the second cleavage site 123 and the fourth modified sgRNA 204 in a reverse orientation (i.e., the same orientation as the first promoter 112) and is operably linked to the first promoter 112.

[0156] In some examples, the nucleic acid sequence of any of the disclosed modified sgRNAs 201, 202, 203, 204, 103 comprises at least 70%, at least 80%, at least 85%, at least 90%, at least 95%, at least 98%, at least 99% or 100% sequence identity to SEQ ID NO: 10, 11, 12, 13, 14, 15, 42, 43, 44, 45, 46, 47, or 48; or consists of or comprises SEQ ID NO: 10, 11, 12, 13, 14, 15, 42, 43, 44, 45, 46, 47, or 48.

[0157] In some examples, the nucleic acid sequence encoding the first modified sgRNA201 comprises at least 70%, at least 80%, at least 85%, at least 90%, at least 95%, at least 98%, at least 99%, or 100% sequence identity to SEQ ID NO: 10, 12, or 13; or comprises or consists of SEQ ID NO: 10, 11, or 13. In some examples, the nucleic acid sequence encoding the second modified sgRNA202 comprises at least 70%, at least 80%, at least 85%, at least 90%, at least 95%, at least 98%, at least 99%, or 100% sequence identity to SEQ ID NO: 10, 11, 13, or 14; or comprises or consists of SEQ ID NO: 10, 11, 13, or 14. In some examples, the nucleic acid sequence encoding the third modified sgRNA 203 comprises at least 70%, at least 80%, at least 85%, at least 90%, at least 95%, at least 98%, at least 99%, or 100% sequence identity to SEQ ID NO: 10, 11, 14, or 15; or comprises or consists of SEQ ID NO: 10, 11, 14, or 15. In some examples, the nucleic acid sequence encoding the fourth modified sgRNA 204 comprises at least 70%, at least 80%, at least 85%, at least 90%, at least 95%, at least 98%, at least 99%, or 100% sequence identity to SEQ ID NO: 10, 11, 12, 13, 14, or 15; or comprises or consists of SEQ ID NO: 10, 11, 12, 13, 14, or 15.

[0158] In non-limiting examples, the nucleic acid molecule encoding the multiple sgRNA200 comprises at least 70%, at least 80%, at least 85%, at least 90%, at least 95%, at least 98%, at least 99%, or 100% sequence identity to SEQ ID NO: 3, 4, 5, 6, 53, 54, or 55. In some examples, the nucleic acid molecule encoding the multiple sgRNA200 comprises at least 95% sequence identity to SEQ ID NO: 3, 4, 5, 6, 53, 54, or 55. In further examples, the nucleic acid molecule encoding the multiple sgRNA200 comprises or consists of SEQ ID NO: 3, 4, 5, 6, 53, 54, or 55.

[0159] Exemplary targeting sequences The disclosed crRNA101, 102, 103 and modified sgRNA201, 202, 203, 204, 103 contain targeting sequences that facilitate targeting of Cas9 to a sequence of interest. The targeting sequences are selected independently for each crRNA101, 102, 103 or modified sgRNA201, 202, 203, 204, 103. Thus, the crRNA101, 102, 103 or modified sgRNA201, 202, 203, 204, 103 contained in the multiple crRNA100 or multiple sgRNA200 may contain the same targeting sequence, different sequences, or a combination thereof. Thus, each individual crRNA101, 102, 103 or modified sgRNA201, 202, 203, 204, 103 may target the same gene, different genes, or a combination thereof.

[0160] The targeting sequence has sufficient complementarity to hybridize with the target sequence (e.g., a sequence found in a gene of interest or in the promoter or regulatory element of the gene of interest). In some examples, the target sequence is targeted to modulate the expression of the target gene. For example, activate the expression of the target gene. In some examples, the targeting sequence has sufficient complementarity with the target sequence to hybridize with the target sequence and direct the sequence-specific binding of Cas9 or dCas9 to the target sequence.

[0161] In some examples, the degree of complementarity between the targeting sequence and its corresponding target sequence is about 50%, about 60%, about 70%, about 80%, about 85%, about 90%, about 95%, about 97.5%, about 98%, about 99% or 100% when optimally aligned. In certain examples, the degree of complementarity between the targeting sequence and its corresponding target sequence is about 90% or more. In certain examples, the degree of complementarity between the targeting sequence and its corresponding target sequence is about 95% or more. Optimal alignment can be determined using any suitable algorithm for aligning sequences. Non-limiting examples include the Smith-Waterman algorithm, the Needleman-Wunsch algorithm, algorithms based on the Burrows-Wheeler transformation (e.g., Burrows Wheeler Aligner), ClustalW, Clustal X, BLAT, Novoalign (Novocraft Technologies, ELAND (Illumina, San Diego, Calif.), SOAP (available at soap.genomics.org.cn), and Maq (available at maq.sourceforge.net).

[0162] In some embodiments, the targeting sequence is about 14-30 nucleotides in length. For example, about 14, about 15, about 16, about 17, about 18, about 19, about 20, about 21, about 22, about 23, about 24, about 25, about 26, about 27, about 28, about 29 or about 30 nucleotides in length. In further examples, the targeting sequence is about 14-28, about 14-26, about 14-24, about 14-22, about 14-20, about 14-18, about 14-17, about 14-16, about 14-15, about 16-30, about 18-30, about 20-30, about 22-30, about 24-30, about 26-30, about 28-30 nucleotides. In a specific non-limiting example, the targeting sequence is about 14-16 nucleotides.

[0163] In some examples, the targeting sequence is complementary to the sequence near the transcription start site of the target gene, for example, in the promoter region of the target gene.In some examples, the targeting sequence is complementary to the sequence within about 10, about 25, about 50, about 60, about 70, about 80, about 90, about 100, about 110, about 120, about 130, about 140, about 150, about 175, about 200, about 300, about 400 or about 500 nucleotides of the transcription start site. In further examples, the targeting sequence may be located within about 1-50, about 1-100, about 1-150, about 1-200, about 1-300, about 1-400, about 1-500, about 10-500, about 50-500, about 100-500, about 150-500, about 200-500, about 250-500, about 300-500, about 350-500, about 400-500, about 10-50, about 10-100, about 10-150, about 10-200, about 10-250, about 10-300, about 10-350, about 1 The targeting sequence is complementary to a sequence located within about 0-400, about 10-450, about 25-50, about 25-100, about 25-150, about 25-200, about 25-250, about 25-300, about 25-350, about 25-400, about 25-450, about 50-100, about 50-150, about 50-200, about 50-250, about 50-300, about 50-350, about 50-400, about 50-450, about 100-200, about 100-250, about 100-300, or about 100-400 nucleotides. In a specific, non-limiting example, the targeting sequence is complementary to a sequence located within about 200 nucleotides of the transcription start site.

[0164] Targeting sequence can be designed to target multiple genes.For example, targeting sequence can be designed to target sequences that are conserved among a group of gene targets.For example, target sequences that are conserved among about 2, about 3, about 4, about 5, about 6, about 7, about 8, about 9, about 10 or more target genes.Therefore, the term "target" used in relation to gene includes a single gene target, or multiple gene targets that can be targeted by a single targeting sequence.

[0165] In some embodiments, gene target is a gene whose decreased expression leads to disease or disorder in a subject, or whose increased expression can alleviate the symptoms of disease or disorder.Therefore, activated gene expression is desired.Non-limiting examples of disease and exemplary gene target for activation are shown in Table 1 and Table 2 below. [Table 1-1] [Table 1-2]

[0166] Additional non-limiting examples of gene targets and diseases are provided in Table 2. [Table 2-1] [Table 2-2] [Table 2-3]

[0167] Additional examples can be found in US Pat. No. 10,550,372.

[0168] In some examples, the crRNA (e.g., 101, 102, 103) or modified sgRNA (e.g., 201, 202, 203, 204, 103) targets a gene for which activated expression is desired, for example, one or more genes listed in Table 1 or Table 2. In some examples, the gene target is activated by using a targeting sequence complementary to the promoter or regulatory region of the target gene, for example, one or more genes listed in Table 1 or Table 2. In certain non-limiting examples, the crRNA (e.g., 101, 102, 103) or modified sgRNA (e.g., 201, 202, 203, 204, 103) comprises a targeting sequence complementary to a sequence in the promoter region of EEF1α2, Fst, Pdx1, Klotho, utrophin, interleukin 10, Six2, OCT4, SOX2, KLF4, c-MYC, MyoD, Mef2b, or Pax7. In another non-limiting example, the crRNA (e.g., 101, 102, 103) or modified sgRNA (e.g., 201, 202, 203, 204, 103) comprises a targeting sequence complementary to a sequence in the promoter region of utrophin, EEF1a2, or Fst. In further examples, the crRNA (e.g., 101, 102, 103) or modified sgRNA (e.g., 201, 202, 203, 204, 103) comprises a targeting sequence complementary to a sequence in the promoter region of utrophin, EEF1a2, or Klotho. In some examples, the crRNA (e.g., 101, 102, 103) or modified sgRNA (e.g., 201, 202, 203, 204, 103) comprises a targeting sequence complementary to a sequence in the promoter region of utrophin. In another specific non-limiting example, the crRNA (e.g., 101, 102, 103) or modified sgRNA (e.g., 201, 202, 203, 204), 103 comprises a targeting sequence complementary to a sequence in the promoter region of Foxa3, Gata4, HNF1a, HNF4a.

[0169] Exemplary Modified MS2 Binding Loops In some embodiments, the modified sgRNA (e.g., 201, 202, 203, 204, 103) or modified tracrRNA (e.g., 130) comprises two or more modified MS2-binding loops. The sequence of the modified MS2-binding loop contains at least two nucleotide changes from the native MS2-binding loop sequence of ggccaacatgaggatcacccatgtctgcagggcc (SEQ ID NO: 16), thereby increasing the GC content and / or shortening the repetitive content of the modified MS2-binding loop sequence compared to the native MS2-binding loop sequence. For example, the modified MS2 binding loop sequence can include about 2, about 3, about 4, about 5, about 6, about 7, about 8, about 9 or about 10 nucleotide changes relative to the native MS2 binding loop sequence ggccaacatgaggatcacccatgtctgcagggcc (SEQ ID NO: 16) that increase the GC content of the native sequence, e.g., increase the GC content by about 5%, about 10%, about 15%, about 20%, about 25%, about 30%, about 35%, about 40%, about 45%, about 50% or more. In a further example, there are at least four nucleotide changes. Suitable percentage increases include, for example, about 1-5%, about 1-8%, about 1-10%, about 1-12%, about 1-15%, about 1-20%, about 1-30%, about 1-40%, about 1-50%, about 1-60%, about 5-10%, about 5-20%, about 5-30%, about 5-40%, about 5-50%, about 5-60%, about 10-20%, about 10-30%, about 10-40%, about 10-50%, about 10-60%, about 20-30%, about 20-40%, about 20-50%, about 20-60%, about 30-40%, about 30-50%, about 30-60%, about 40-50%, about 40-60%, or about 50-60%. In some examples, the GC content of the nucleic acid molecule is increased by adding "G" and / or "C" nucleotides to the molecule, by substituting one or more native "A"s with "G", or substituting one or more native "T"s with "C", or a combination thereof. In some examples, the modified MS2 binding loop sequence contains about two nucleotide changes, thereby increasing the GC content of the MS2 binding loop sequence.In some instances, the modified MS2 binding loop sequence contains about six nucleotide changes, thereby increasing the GC content of the MS2 binding loop sequence.

[0170] In some examples, the nucleotide changes to the native MS2 binding loop sequence shorten the repetitive content, such as reducing the repetitive content by about 5%, about 8%, about 10%, about 15%, about 20%, about 30%, about 40%, or about 50% or more. In some examples, the decrease is about 1-5%, about 1-8%, about 1-10%, about 1-15%, about 5-10%, about 5-20%, about 5-30%, about 5-40%, about 5-50%, about 5-60%, about 5-75%, about 10-20%, about 10-30%, about 10-40%, about 10-50%, about 10-60%, about 10-75%, about 20-30%, about 20-40%, about 20-50%, about 20-60%, about 20-75%, about 30-40%, about 30-50%, about 30-60%, about 30-75%, about 40-50%, about 40-60%, about 40-75%, about 50-60%, or about 50-75%. In some examples, the modified MS2 binding loop sequence contains about 2 nucleotide changes, thereby reducing the repetitive content of the MS2 binding loop sequence. In some examples, the modified MS2 binding loop sequence contains about 6 nucleotide changes, thereby reducing the repetitive content of the MS2 binding loop sequence. In further examples, the repetitive content is shortened or reduced by deleting one or more repetitive nucleotides.

[0171] In particular examples, the modified MS2 binding loop sequence comprises at least 70%, at least 80%, at least 85%, at least 90%, at least 95%, at least 98%, at least 99% or 100% sequence identity to one or more of SEQ ID NOs: 17, 18 or 19. In non-limiting examples, the modified MS2 binding loop sequence comprises at least 95% sequence identity to one or more of SEQ ID NOs: 17, 18 or 19. In further examples, the modified MS2 binding loop sequence comprises or consists of the sequence tgctgaacatgaggatcacccatgtctgcagcagca (SEQ ID NO: 17), gggccaacatgaggatcacccatgtctgcagggccc (SEQ ID NO: 18), or ggccagcatgaggatcacccatgcctgcagggcc (SEQ ID NO: 19).

[0172] Exemplary Promoters The promoter (e.g., the first or second promoter of the multiple crRNA or multiple sgRNA, e.g., 110, 111, 112, 113) can be any suitable promoter. For example, a pol III promoter (e.g., a U6 or H1 promoter); a pol II promoter (e.g., a retroviral Rous sarcoma virus (RSV) LTR promoter, optionally with an RSV enhancer); a cytomegalovirus (CMV) promoter, optionally with a CMV enhancer; an SV40 promoter; a dihydrofolate reductase promoter; a β-actin promoter; a phosphoglycerol kinase (PGK) promoter; Spc5.12 (muscle-specific); CW3SL; and / or an EF1α promoter. In some examples, the promoter is specific to a particular cell type or organ (e.g., Spc5.12). In other examples, the promoter is ubiquitous (e.g., EF1α). In some examples, the promoter is a minimal promoter such as the cytomegalovirus (CMV), human b-actin (hACTB), human elongation factor-1a (hEF-1a) and / or cytomegalovirus early enhancer / chicken b-actin (CAG) promoter (e.g., promoters described in Papadakis et al., Current Gene Therapy, 4:89-113, 2004; Damdindorj et al., PLoS ONE 9(8):e106472, 2014). In one example, one or more of promoters 110, 111, 112, 113 are liver-specific promoters such as albumin promoter, hepatitis B virus core protein promoter, hemopexin promoter, or human alpha 1-antitrypsin promoter.

[0173] In some examples, the first promoter 110, 112 and the second promoter 111, 113 consist of or include different sequences. In other examples, the first promoter 110, 112 and the second promoter 111, 113 consist of or include the same sequence. In some examples, the first promoter 110, 112 and / or the second promoter 111, 113 are mU6, hU6, H1 or 7SK promoters. In specific, non-limiting examples, the first promoter 110, 112 is hU6 or mU6 and the second promoter 111, 113 is hU6 or mU6. In some examples, the promoters 110-113 confer tropism to a particular tissue or cell type, for example, Spc 5.12 (muscle specific) or Col1a2 (fibroblast specific), or are inducible in response to a stimulus. It will be appreciated by those skilled in the art that promoter selection may depend on factors such as the choice of tissue or cellular target, the host cell to be transformed, the desired expression level, and the like.

[0174] Exemplary Cleavage Sites The cleavage site, e.g., the first cleavage site 120 or the second cleavage site 121 of the multiple crRNA, or the first cleavage site 122 or the second cleavage site 123 of the multiple sgRNA, is a sequence that can be cleaved when transcribed into RNA. Suitable cleavage mechanisms include self-cleavage, e.g., a self-cleaving ribozyme, or cleavage by endogenous mechanisms of the host cell, e.g., pre-tRNA cleavage.

[0175] In some examples, the cleavage sites (e.g., 120, 121, 122, 123) are self-cleaving RNAs. In some examples, the cleavage sites (e.g., 120, 121, 122, 123) comprise or consist of a pre-tRNA sequence. In other examples, the cleavage sites (e.g., 120, 121, 122, 123) comprise or consist of a self-cleaving ribozyme, such as the Hepatitis Delta Virus Hammerhead Ribozyme (HDV-HH). The first cleavage site 120, 122 and the second cleavage site 121, 123 may comprise or consist of different sequences, or may comprise or consist of the same sequence. In a specific, non-limiting example, the first cleavage site 120, 122 is a pre-tRNA sequence and the second cleavage site 121, 123 is a self-cleaving ribozyme, such as a hammerhead. In other non-limiting examples, the first cleavage site 120, 122 is a pre-tRNA sequence and the second cleavage site 121, 123 is also a pre-tRNA sequence. In some examples, the first cleavage site 120, 122 is a pre-tRNA sequence and the second cleavage site 121, 123 is a pre-tRNA sequence from a different organism. In a non-limiting example, one cleavage site can be a pre-tRNA from yeast and the other can be a pre-tRNA from a plant, such as Zea mays. In a particular non-limiting example, the first cleavage site 120 of the multiple crRNA 100 comprises or consists of SEQ ID NO: 20 or SEQ ID NO: 21 and the second cleavage site 121 comprises or consists of SEQ ID NO: 22. In other particular non-limiting examples, the first cleavage site 122 of the multiple sgRNA 200 comprises or consists of SEQ ID NO: 20 or SEQ ID NO: 21 and the second cleavage site 123 of the multiple sgRNA 200 comprises or consists of SEQ ID NO: 20 or SEQ ID NO: 21.

[0176] A. A vector containing multiple crRNAs and multiple sgRNAs Also provided are vectors, such as viral vectors (e.g., retroviruses, lentiviruses, adenoviruses, adeno-associated viruses, or herpes simplex viruses) or plasmids that contain one or more nucleic acid molecules encoding multiple crRNAs, multiple sgRNAs, or both. In some examples, the vector is an AAV vector, such as an AAV1 vector, an AAV2 vector, an AAV3 vector, an AAV4 vector, an AAV5 vector, an AAV6 vector, an AAV7 vector, an AAV8 vector, an AAV9 vector, an AAV10 vector, an AAV11 vector, an AAV12 vector, an AAV-PHP.B vector, an AAV-PHP.eB vector, or an AAV-PHP.S vector. In certain non-limiting examples, the vector is an AAV9 vector. In some examples, the vector is an adenoviral vector, such as Ad5. The vector may contain other elements, such as a selection marker, such as an antibiotic, e.g., puromycin, hygromycin, or a gene encoding a detectable marker, such as a fluorophore (e.g., GFP or RFP) or a luciferase protein. Vectors can include naturally occurring or non-naturally occurring nucleotides or ribonucleotides. The disclosed vectors can be used in the methods, compositions and kits provided herein.

[0177] B. Compositions and kits comprising multiple crRNAs and multiple sgRNAs Also provided are compositions and kits comprising the multiple crRNAs or multiple sgRNAs provided herein, or one or more nucleic acids encoding one or more multiple crRNAs or multiple sgRNAs provided herein. For example, the compositions may comprise one or more nucleic acids encoding the disclosed multiple crRNAs or multiple sgRNAs, the disclosed RNA molecules encoded by the multiple crRNAs or multiple sgRNAs, the disclosed vectors encoding the multiple crRNAs or multiple sgRNAs, or the ribonucleoprotein (RNP) complexes comprising the multiple crRNAs or multiple sgRNAs, and a pharma- ceutically acceptable carrier (e.g., saline, water, or PBS). In some examples, the multiple crRNAs or multiple sgRNAs, or one or more nucleic acids encoding those RNAs, are present in cells that are part of the composition. In some examples, the composition is liquid, lyophilized powder, or frozen.

[0178] The composition is suitable for formulation and administration in vitro or in vivo. Suitable carriers and their formulations are described in Remington: The Science and Practice of Pharmacy, 22nd Edition, Loyd V. Allen et al., editors, Pharmaceutical Press (2012). Pharmaceutically acceptable carriers include materials that are not biologically or otherwise undesirable, i.e., the material is administered to a subject without causing undesirable biological effects or interacting in a deleterious manner with other components of the pharmaceutical composition in which it is contained. When administered to a subject, the carrier is selected to minimize the degradation of the active ingredient (e.g., the vector containing multiple crRNAs and / or multiple sgRNAs) as necessary and to minimize adverse side effects in the subject.

[0179] In some embodiments, the disclosed compositions for administration are dissolved in a pharma- ceutically acceptable carrier, such as an aqueous carrier. A variety of aqueous carriers can be used, such as buffered saline, etc. These solutions can be sterile and generally free of undesirable substances. These compositions can be sterilized. The compositions can contain pharma-ceutically acceptable auxiliary substances required to approximate physiological conditions, such as pH adjusting and buffering agents, toxicity adjusting agents, etc., such as sodium acetate, sodium chloride, potassium chloride, calcium chloride, sodium lactate, etc. The concentration of the active agent in these formulations can vary and can be selected primarily based on bodily fluid volume, viscosity, body weight, etc., according to the particular mode of administration selected and the needs of the subject.

[0180] Pharmaceutical preparations can be prepared by mixing the disclosed nucleic acid molecules, RNA molecules, vectors, or RNP complexes having the desired purity with any pharma- ceutically acceptable carrier, excipient, or stabilizer. Such preparations can be lyophilized preparations or aqueous solutions.

[0181] Acceptable carriers, excipients or stabilizers are non-toxic to recipients at the dosage and concentration used.Acceptable carriers, excipients or stabilizers can be acetate, phosphate, citrate and other organic acids; antioxidants (e.g., ascorbic acid) preservatives, and low molecular weight polypeptides; proteins such as serum albumin or gelatin, or hydrophilic polymers such as polyvinylpyrrolidone; and amino acids, monosaccharides, disaccharides, and other carbohydrates, including glucose, mannose, or dextrin; chelating agents; ionic and nonionic surfactants (e.g., polysorbates); salt-forming counterions such as sodium; metal complexes (e.g., Zn-protein complexes); and / or nonionic surfactants.

[0182] Formulations suitable for oral administration can include: (a) liquids such as an effective amount of the disclosed nucleic acid molecules, RNA, or vectors, RNP complexes, or combinations thereof suspended in a diluent such as water, saline, or PEG 400; (b) capsules, sachets, or tablets containing a predetermined amount of the active ingredient as a liquid, solid, granules, or gelatin, respectively; (c) a suspension in a suitable liquid; and (d) a suitable emulsion. Tablet forms can include one or more of lactose, sucrose, mannitol, sorbitol, calcium phosphate, corn starch, potato starch, microcrystalline cellulose, gelatin, colloidal silicon dioxide, talc, magnesium stearate, stearic acid, and other excipients, colorants, fillers, binders, diluents, buffers, wetting agents, preservatives, flavorings, dyes, disintegrants, and pharma- ceutically compatible carriers. Lozenge forms can contain the active ingredient in a flavoring, such as sucrose, and can also include pastilles which contain the active ingredient in an inert base, such as an emulsion, gel of gelatin and glycerin or sucrose and acacia, which contains a carrier in addition to the active ingredient.

[0183] The disclosed nucleic acid molecules (e.g., DNA, e.g., cDNA), RNA molecules, vectors, or RNP complexes, alone or in combination with other suitable components, can be made into aerosol formulations (i.e., they can be "nebulized") to be administered via inhalation. Aerosol formulations can be placed into pressurized acceptable propellants, such as dichlorodifluoromethane, propane, nitrogen, and the like.

[0184] Formulations suitable for parenteral administration, such as by intra-articular (into a joint), intravenous, intramuscular, intratumoral, intradermal, intraperitoneal, and subcutaneous routes, include aqueous and non-aqueous isotonic sterile injection solutions that may contain antioxidants, buffers, bacteriostats, and solutes that render the formulation isotonic with the blood of the intended recipient, as well as aqueous and non-aqueous sterile suspensions that may contain suspending agents, solubilizers, thickening agents, stabilizers, and preservatives. In the provided methods, the compositions may be administered, for example, by intravenous injection, orally, topically, intraperitoneally, intravesically, intratumorally, or intrathecally. Parenteral, intratumoral, and intravenous administration are preferred methods of administration. Formulations of the compounds may be provided in unit-dose or multi-dose sealed containers, such as ampoules and vials.

[0185] Injection solutions and suspensions can be prepared from sterile powders, granules, and tablets of the kind previously described. For ex vivo therapy, cells transduced or infected with the disclosed nucleic acids may also be administered intravenously or parenterally as described above.

[0186] Pharmaceutical preparations can be in unit dosage form. In such form, the preparation is divided into unit doses containing an appropriate amount of active ingredient. Thus, pharmaceutical compositions can be administered in various unit dosage forms depending on the method of administration. For example, unit dosage forms suitable for oral administration include, but are not limited to, powder, tablets, pills, capsules and lozenges.

[0187] Also provided are kits that include one or more nucleic acids encoding the disclosed multiple crRNAs or multiple sgRNAs (which may be part of a vector, such as an AAV vector, and / or may be present in a cell, such as a mammalian cell) or one or more multiple crRNAs or multiple sgRNAs provided herein. The kits may further include a nucleic acid encoding a Cas9 protein or a dCas9 protein (which may be part of a vector, such as an AAV vector, and / or may be present in a cell, such as a mammalian cell). In some examples, the kits may further include a nucleic acid encoding an MS2 transcription activator fusion protein (e.g., MS2-p65-HSF1), which may be part of a vector (e.g., an AAV vector) and / or may be present in a cell, such as a mammalian cell. In some examples, the nucleic acid encoding the Cas9 protein or the dCas9 protein and the nucleic acid encoding the MS2 transcription activator fusion protein are part of a single viral vector (e.g., an AAV vector). In some examples, the nucleic acid encoding the MS2 transcription activator fusion protein encodes a sequence that encodes a protein sequence having at least 90%, at least 95%, at least 98%, at least 99%, or 100% sequence identity to MS2-p65-HSF1, e.g., SEQ ID NO:35.

[0188] In one example, the composition or kit comprises a ribonucleoprotein (RNP) complex (e.g., mTGA complex) comprised of one or more Cas9 or dCas9 proteins and one or more disclosed crRNAs and modified tracrRNAs, or modified sgRNAs, and one or more transcriptional activators (e.g., MS2-p65-HSF1). In some examples, the RNP complex comprises a disclosed crRNA and modified tracrRNA. In further examples, the RNP complex comprises a disclosed modified sgRNA (including a disclosed dgRNA).

[0189] In a further example, the composition or kit comprises a vector encoding a Cas9 or dCas9 protein and a vector encoding one or more of the disclosed crRNAs or modified sgRNAs (including dgRNAs) and encoding an MS2 transcription activator fusion protein. In one example, the composition or kit comprises a cell, such as a bacterial cell or a eukaryotic cell, that comprises a Cas9 or dCas9 protein, a Cas9 or dCas9 protein coding sequence, a crRNA or modified sgRNA molecule, a nucleic acid encoding an MS2 transcription activator fusion protein, an MS2 transcription activator fusion protein (e.g., MS2-p65-HSF1), or a combination thereof. In one example, the composition or kit comprises a cell-free system comprising a Cas9 or dCas9 protein, a Cas9 or dCas9 protein coding sequence, a disclosed RNA molecule (e.g., crRNA, modified tracrRNA, modified sgRNA, multiple crRNA, multiple sgRNA), a nucleic acid encoding multiple crRNAs or multiple sgRNAs, an MS2 transcriptional activator fusion protein (e.g., MS2-p65-HSF 1), a nucleic acid encoding an MS2 transcriptional activator fusion protein, or a combination thereof.

[0190] In some examples, the kit includes a delivery system (e.g., a liposome, particle, exosome, microvesicle, viral vector or plasmid) and / or a label (e.g., a peptide or antibody that can be directly conjugated to either the RNP or a particle containing the RNP to direct cell type specific uptake / enhance endosomal escape / enable blood-brain barrier crossing, etc.). In some examples, the kit further includes a cell culture or growth medium, such as a medium suitable for growing bacterial, plant, insect, or mammalian cells. In some examples, the components of the kit are in separate containers (such as glass or plastic vials).

[0191] C. Cells containing multiple crRNAs and multiple sgRNAs Cells are provided that contain multiple crRNAs or multiple sgRNAs provided herein, or one or more nucleic acids encoding one or more multiple crRNAs or multiple sgRNAs provided herein. In some examples, such cells also contain Cas9 or dCas9 proteins. In some examples, such cells also contain MS2 transcription activator fusion proteins. Nucleic acid molecules encoding multiple crRNAs and multiple sgRNAs (including their RNA molecules), as well as nucleic acid molecules encoding Cas9, dCas9, and / or MS2 transcription activator fusion proteins, can be introduced into cells to generate transformed (e.g., recombinant) cells. Such recombinant cells can be used in the methods, compositions, and kits provided herein. In some examples, such cells are generated by introducing Cas9, dCas9, and / or MS2 transcription activator fusion proteins and one or more multiple crRNA molecules and multiple sgRNA molecules into cells, for example, as a ribonucleoprotein (RNP) complex.

[0192] Such recombinant cells can be eukaryotic or prokaryotic. Examples of such cells include, but are not limited to, bacteria, archaea, plants, fungi, yeast, insects, and mammalian cells, such as Lactobacillus, Lactococcus, Bacillus (e.g., B.subtilis), Escherichia (e.g., E.coli), Clostridium, Saccharomyces or Pichia (e.g., S.cerevisiae or P.pastoris), Kluyveromyces lactis, Salmonella typhimurium, Drosophila cells, C.elegans cells, Xenopus cells, SF9 cells, C129 cells, 293 cells, Neurospora, and immortalized mammalian cell lines (e.g., Hela cells, myeloid cell lines, hepatic cell lines, and lymphoid cell lines). In one example, the cell is a prokaryotic cell, such as a bacterial cell, such as E.coli.

[0193] In one example, the cell is a eukaryotic cell, such as a mammalian cell, such as a human cell. In one example, the cell is a primary eukaryotic cell, a stem cell, a tumor / cancer cell, a circulating tumor cell (CTC), a blood cell (e.g., T cell, B cell, NK cell, Treg, etc.), a hematopoietic stem cell, a specialized immune cell (e.g., tumor-infiltrating lymphocyte or tumor-suppressing lymphocyte), a stromal cell in the tumor microenvironment (e.g., cancer-associated fibroblast, etc.), a pancreatic cell, a kidney cell, a liver cell, or a muscle cell. In one example, the cell is a brain cell (e.g., a neuron, an astrocyte, a microglia, a retinal ganglion cell, a rod / cone, etc.) of the central or peripheral nervous system.

[0194] In one example, the cell is part of (or is obtained from) a biological sample, such as a biological specimen containing genomic DNA, RNA (e.g., mRNA), protein, or a combination thereof, obtained from a subject. Examples include, but are not limited to, peripheral blood, serum, plasma, urine, saliva, sputum, tissue biopsy, fine needle aspirate, surgical specimen, and autopsy material.

[0195] In one example, the cell is a tumor, e.g., a hematological tumor (e.g., acute leukemia (e.g., acute lymphocytic leukemia, acute myelocytic leukemia, acute myeloid leukemia, and leukemias including myeloblastic, promyelocytic, myelomonocytic, monocytic, and erythroleukemia), chronic leukemia (e.g., chronic myelocytic (granulocytic) leukemia, chronic myeloid leukemia, and chronic lymphocytic leukemia), polycythemia vera, lymphoma, Hodgkin's disease, non-Hodgkin's lymphoma (including low grade, intermediate grade, and high grade), multiple myeloma, Waldenstrom's macroglobulinemia, heavy chain disease, myelodysplastic syndrome, mantle cell lymphoma, and myelodysplasia) or a solid tumor (e.g., sarcoma and cancer: from fibrosarcoma, myxosarcoma, liposarcoma, chondrosarcoma, osteogenic sarcoma and other sarcomas, synovium, mesothelioma, Ewing's tumor, leiomyosarcoma, rhabdomyosarcoma, colon cancer, lymphoid malignancies, pancreatic cancer, breast cancer, lung cancer, ovarian cancer, prostate cancer, hepatocellular carcinoma, squamous cell carcinoma, basal cell carcinoma, adenocarcinoma, sweat gland carcinoma, sebaceous gland carcinoma, papillary carcinoma, papillary adenocarcinoma, medullary carcinoma, bronchogenic carcinoma, renal cell carcinoma, hepatoma, cholangiocarcinoma, choriocarcinoma, Wilms' tumor, cervical cancer, testicular tumors, bladder cancer, and CNS tumors (such as glioma, astrocytoma, medulloblastoma, craniopharyngioma, ependymoma, pinealoma, hemangioblastoma, acoustic neuroma, oligodendroglioma, meningioma, melanoma, neuroblastoma, and retinoblastoma).

[0196] IV. Multiplex Targeted Gene Activation (mTGA) System A multiple targeted gene activation (mTGA) system is also provided. The system may include a first vector (e.g., a viral vector, e.g., AAV, or lentiviral vector) that includes a nucleic acid encoding Cas9 or dCas9 (whose expression may be driven by a promoter), and a second vector (e.g., a viral vector, e.g., AAV, or lentiviral vector) that includes one or more nucleic acids encoding one or more of the multiple crRNAs or multiple sgRNAs disclosed herein and a nucleic acid encoding an MS2 transcription activator fusion protein (e.g., MS2-p65-HSF1, whose expression may be driven by a promoter). In some examples, the nucleic acid encoding the MS2 transcription activator fusion protein encodes a sequence that encodes a protein sequence that has at least 90%, at least 95%, at least 98%, at least 99%, or 100% sequence identity to MS2-p65-HSF1, e.g., SEQ ID NO:35.

[0197] In some examples, the first and second vectors are adeno-associated virus (AAV) vectors (e.g., AAV1 vector, AAV2 vector, AAV3 vector, AAV4 vector, AAV5 vector, AAV6 vector, AAV7 vector, AAV8 vector, AAV9 vector, AAV10 vector, AAV11 vector, AAV12 vector AAV-PHP.B vector, AAV-PHP.eB vector, or AAV-PHP.S vector) or adenovirus vectors (e.g., Ad5). In one example, the first and second vectors are AAV9 or Ad5 vectors. In some examples, the first and first and second vectors are AAV8 vectors. In some examples, the AAV vector used has tropism for a particular tissue or cell type, such as kidney cells, muscle cells, or pancreatic cells.

[0198] In some examples, the first vector comprises a nucleic acid encoding a Cas9 protein, such as a Streptococcus pyogenes Cas9 protein. In some examples, the first vector comprises a nucleic acid encoding a Cas9 protein, such as a nucleic acid molecule encoding a protein having at least 90%, at least 95%, at least 98%, at least 99%, or 100% sequence identity to SEQ ID NO: 31, and the Cas9 protein has endonuclease activity. In some examples, the first vector comprises a nucleic acid encoding a dCas9 protein, such as a dCas9 protein with reduced or no endonuclease activity. In some examples, the first vector comprises a nucleic acid encoding a dCas9 protein, such as a nucleic acid molecule encoding a protein having at least 90%, at least 95%, at least 98%, at least 99%, or 100% sequence identity to SEQ ID NO: 33, and the dCas9 protein has reduced endonuclease activity or endonuclease activity. In some examples, the dCas9 protein encoded by the nucleic acid molecule has a mutation at D10A, E762A, D839A, H840A, N854A, N863A, D986A, or a combination thereof.

[0199] In some examples, the first vector comprises a nucleic acid encoding a Cas9 or dCas9 protein and does not encode a transcription activator, such as VP64, P65, MyoD1, HSF1, RTA, SET7 / 9, or any combination thereof. Thus, in some examples, the Cas9 or dCas9 protein encoded by the first vector is not a Cas9 transcription activator fusion protein or a dCas9 transcription activator fusion protein.

[0200] The second vector comprises one or more nucleic acids encoding multiple crRNAs or multiple sgRNAs disclosed herein, such as those having at least 90%, at least 95%, at least 98%, at least 99% or 100% sequence identity to SEQ ID NO: 1, 2, 3, 4, 5, 6, 53, 54 or 55. In one example, the encoded multiplexed crRNAs or modified sgRNAs have at least 95% sequence identity to SEQ ID NO: 1, 2, 3, 4, 5, 6, 53, 54 or 55.

[0201] The second vector also includes a nucleic acid encoding an MS2 transcription activator fusion protein. The MS2 transcription activator fusion protein includes an MS2 domain fused directly or indirectly (e.g., via a linker) to a transcription activation domain. Exemplary transcription activation domains include VP64, P65, MyoD1, HSF1, RTA, SET7 / 9, or any combination thereof. In some examples, the nucleic acid encoding the MS2 transcription activator fusion protein encodes a sequence encoding a protein sequence having at least 90%, at least 95%, at least 98%, at least 99%, or 100% sequence identity to MS2-p65-HSF1, e.g., SEQ ID NO:35.

[0202] In some examples, the mTGA system allows for targeting multiple genes. In some examples, the mTGA system further comprises one or more additional multiple crRNAs, multiple sgRNAs, crRNAs, modified sgRNAs (including dgRNAs). The additional multiple crRNAs, multiple sgRNAs, crRNAs, or modified sgRNAs can be used, for example, to target different genes of interest. Such additional multiple crRNAs, multiple sgRNAs, crRNAs, or modified sgRNAs can be present on additional vectors or can be present on a second vector.

[0203] V. Methods for Targeted Gene Activation Provided herein is a method for increasing (e.g., activating) the expression of at least one gene product in vitro or in a subject. The gene product whose expression is increased can be a gene itself (e.g., DNA), RNA (such as mRNA, miRNA, and non-coding RNA), or a gene product (e.g., protein). When used in vitro, expression can be increased in cells such as eukaryotic or prokaryotic cells, for example, mammalian cells. When used in vivo, expression can be increased in subjects such as mammals (e.g., mice, non-human primates, or other veterinary subjects) or humans.

[0204] Methods of using the disclosed multiplex crRNA, multiplex sgRNA, and mTGA systems are also provided herein. Such methods can be used to increase the expression of at least one target gene product in a subject, for example, a gene whose expression is under-regulated in the subject. In some examples, the disclosed methods treat a disease in a subject caused by under-expression of a gene (causative gene). In some examples, the target gene is a causative gene. In other examples, the target gene is not a causative gene, and instead, increased expression of the target gene compensates for the loss of function of the causative gene, for example, when the target gene is a functional analog of the causative gene. In some examples, the methods increase expression of the target gene or gene product by at least about 10%, about 20%, about 30%, about 40%, about 50%, about 60%, about 70%, about 80%, about 90%, about 95%, about 100%, about 200%, about 300%, about 400%, or about 500%. In further examples, the methods can be used to increase expression of a target gene or gene product by about 10-500%, about 10-400%, about 10-300%, about 10-200%, about 10-100%, about 10-90%, about 10-80%, about 10-70%, about 10-60%, about 10-50%, about 10-40%, about 10-30%, about 10-20%, about 20-500%, about 30-500%, about 40-500%, about 50-500%, about 60-500%, about 70-500%, about 80-900%, about 90-1000%, about 1 ... Increase by 0-500%, about 90-500%, about 100-500%, about 200-500%, about 300-500%, about 400-500%, about 25-100%, about 25-200%, about 50-100%, about 50-200%, about 50-300%, about 50-400%, about 50-500%, about 100-200%, about 100-300%, about 100-400%, about 100-500%, about 200-300%, about 200-400%, or about 200-500%.

[0205] In some examples, the method is an in vivo method of increasing (e.g., activating) expression of at least one gene product in a subject. In some examples, the gene product is a product of a target gene. The method includes administering a therapeutically effective amount of a multiple targeted gene activation (mTGA) system to a subject. Components of the mTGA system infect cells (e.g., cells in the subject, such as muscle, liver, heart, lung, kidney, spinal cord, or stomach cells, such as liver or muscle cells), thereby increasing expression of at least one gene product in the subject.

[0206] In some examples, the method is an in vitro method of increasing (e.g., activating) expression of at least one gene product in a cell or cell-free system. In some examples, the gene product is a product of a target gene. The method includes contacting an effective amount of a multiple targeted gene activation (mTGA) system with a cell or cell-free system. Components of the mTGA system infect an in vitro cell (e.g., a mammalian cell) or are expressed in the cell-free system, thereby increasing expression of at least one gene product in the infected cell or cell-free system.

[0207] The mTGA system is administered according to known methods, such as systemic or local administration. In certain examples, intravenous administration, such as as a bolus or by continuous infusion over a period of time, or intramuscular, intraperitoneal, intraspinal, subcutaneous, intraarticular, intrasynovial, intrathecal, oral, local, intratumoral, or inhalation routes are used. In one example, administration is direct administration to the liver or hepatic vein or hepatic artery. Thus, the disclosed mTGA system can be administered locally via any of several administration routes, including oral, parenteral, intravenous, intraarticular, intraperitoneal, intramuscular, subcutaneous, intracavity, transdermal, intrahepatic, intracranial, intratumoral, intraosseous, spray / inhalation, into the liver or its vasculature, or by bronchoscopic installation. Thus, the composition is administered in several ways, depending on whether local or systemic treatment is desired and the area to be treated.

[0208] An effective amount of the mTGA system disclosed herein may be based, at least in part, on the particular vector used; the size, age, and sex of the individual; and the size and other characteristics of the proliferating cells. For example, for human treatment, at least 10 3 A viral vector of at least 10 viral genomes (vg) is used, e.g. 4 , at least 10 5 , at least 10 6 , at least 10 7 , at least 10 8 , at least 10 9 , at least 10 10 , at least 10 11 , at least 10 12 , at least 10 13 , at least 10 14 , at least 10 15 , at least 10 16 , at least 10 17 , at least 10 18 , at least 10 19 , or at least 10 20 vg / kg body weight, e.g., about 10 3 ~10 20 , 10 9 ~10 16 , 10 12 ~10 15 , or 10 13 ~10 14 vg / kg body weight of viral genome is used.

[0209] The disclosed compositions, e.g., viral vectors (e.g., AAV vectors), can be administered in a single dose or multiple doses (e.g., 2, 3, 4, 6, or more doses). Multiple doses can be administered simultaneously or sequentially (e.g., over the course of days or weeks).

[0210] The mTGA system used in the present method may include (1) a first vector comprising a nucleic acid encoding a Cas9 protein or a dCas9 protein, and (2) a second vector comprising a nucleic acid encoding a multiplexed crRNA or multiplexed sgRNA and an MS2 transcription activator fusion protein disclosed herein. In some examples, the first and second vectors are adeno-associated virus (AAV) vectors, such as AAV1 vectors, AAV2 vectors, AAV3 vectors, AAV4 vectors, AAV5 vectors, AAV6 vectors, AAV7 vectors, AAV8 vectors, AAV9 vectors, AAV10 vectors, AAV11 vectors, AAV12 vectors, AAV-PHP.B vectors, AAV-PHP.eB vectors, or AAV-PHP.S vectors. In one example, the first and second vectors are AAV9 vectors. In some examples, the AAV vectors used have tropism for a particular tissue or cell type, such as kidney cells, skeletal muscle cells, liver cells, or pancreatic cells (examples are provided elsewhere herein).

[0211] When selecting elements for the disclosed mTGA system that allow gene activation without introducing DNA double-strand breaks, it is necessary that either the Cas9 protein or the modified sgRNA used is in a dead form, or both. Thus, in some examples, a dCas9 protein (e.g., SEQ ID NO: 33) is used with multiple crRNAs or multiple sgRNAs. In some examples, a Cas9 protein (e.g., SEQ ID NO: 31) is used with multiple crRNAs or multiple sgRNAs, and the modified sgRNA is a dgRNA.

[0212] In some examples, the first vector comprises a nucleic acid encoding a Cas9 protein, such as a Streptococcus pyogenes Cas9 protein. In some examples, the first vector comprises a nucleic acid encoding a Cas9 protein, such as a nucleic acid molecule encoding a protein having at least 90%, at least 95%, at least 98%, at least 99%, or 100% sequence identity to SEQ ID NO: 31, and the Cas9 protein has endonuclease activity. In some examples, the first vector comprises a nucleic acid encoding a dCas9 protein, such as a dCas9 protein with reduced or no endonuclease activity. In some examples, the first vector comprises a nucleic acid encoding a dCas9 protein, such as a nucleic acid molecule encoding a protein having at least 90%, at least 95%, at least 98%, at least 99%, or 100% sequence identity to SEQ ID NO: 33, and the dCas9 protein has reduced endonuclease activity or endonuclease activity. In some examples, the dCas9 protein encoded by the nucleic acid molecule has a mutation at D10A, E762A, D839A, H840A, N854A, N863A, D986A, or a combination thereof.

[0213] In some examples, the first vector comprises a nucleic acid encoding a Cas9 or dCas9 protein and does not encode a transcription activator, such as VP64, P65, MyoD1, HSF1, RTA, SET7 / 9, or any combination thereof. Thus, in some examples, the Cas9 or dCas9 protein encoded by the first vector is not a Cas9 transcription activator fusion protein or a dCas9 transcription activator fusion protein.

[0214] In some embodiments, the second vector encodes multiple crRNAs or multiple sgRNAs disclosed herein, such as those with at least 90%, at least 95%, at least 98%, at least 99% or 100% sequence identity to SEQ ID NO: 1, 2, 3, 4, 5, 6, 53, 54 or 55. In a non-limiting example, the encoded multiplexed crRNA has at least 95% sequence identity to SEQ ID NO: 1 or 2. In another non-limiting example, the encoded multiplexed sgRNA has at least 95% sequence identity to SEQ ID NO: 3, 4, 5, 6, 53, 54 or 55.

[0215] The second vector also includes a nucleic acid encoding an MS2 transcription activator fusion protein. The MS2 transcription activator fusion protein includes an MS2 domain fused directly or indirectly (e.g., via a linker) to a transcription activation domain. Exemplary transcription activation domains include VP64, P65, MyoD1, HSF1, RTA, SET7 / 9, or any combination thereof. In some examples, the nucleic acid encoding the MS2 transcription activator fusion protein encodes a sequence encoding a protein sequence having at least 90%, at least 95%, at least 98%, at least 99%, or 100% sequence identity to MS2-p65-HSF1, e.g., SEQ ID NO:35.

[0216] In some examples, the mTGA system further comprises one or more additional multiple crRNAs, multiple sgRNAs, crRNAs, or modified sgRNAs (including dgRNAs), or nucleic acid molecules encoding the same. The additional multiple crRNAs, multiple sgRNAs, crRNAs, or sgRNAs, or nucleic acid molecules encoding the same, can be used, for example, to target different genes of interest. Such additional multiple crRNAs, multiple sgRNAs, crRNAs, or modified sgRNAs can be present on additional vectors or can be present on a second vector.

[0217] In one example, Cas9, dCas9 and / or MS2 transcription activator fusion proteins are expressed and purified in recombinant cells such as E. coli. The resulting purified Cas9, dCas9 and / or MS2 transcription activator fusion proteins are then introduced into a cell or organism in which one or more genes can be upregulated, together with one or more of the disclosed encoded multiple crRNAs, multiple sgRNAs or their RNA products. In some examples, Cas9, dCas9 and / or MS2 transcription activator fusion proteins and the encoded multiple crRNAs, multiple sgRNAs or their RNA products are introduced into a cell / organism as separate components. In other examples, purified Cas9, dCas9 and / or MS2 transcription activator fusions are complexed with the disclosed RNA molecules (e.g., the disclosed multiple crRNA or multiple sgRNA RNA molecules) and this ribonucleoprotein (RNP) complex is introduced into a target cell (e.g., using transfection or injection). In some examples, Cas9, dCas9 and / or MS2 transcription activator fusion proteins and RNA molecules (or nucleic acid molecules encoding same) are injected into embryos (e.g., human, mouse, zebrafish, or Xenopus embryos). Once inside the cell, the Cas9 or dCas9 protein, MS2 transcription activator fusion protein, and RNA molecules (or nucleic acid molecules encoding same) can activate expression of one or more target nucleic acid molecules.

[0218] In a cell or organism, one or more nucleic acid molecules or genes, for example, about 1, about 2, about 3, about 4, or about 5, about 6, about 7, about 8, about 9, or about 10 different nucleic acid molecules or genes, can be targeted by the disclosed methods. In some examples, about 1-10, about 1-9, about 1-8, about 1-7, about 1-6, about 1-5, about 1-4, about 1-3, about 1-2, about 2-10, about 3-10, about 4-10, about 5-10, about 6-10, about 7-10, about 8-10, about 9-10, about 2-4, about 2-6, about 2-8, about 2-10, about 4-6, about 4-8, about 4-10, about 6-8, about 6-10, or about 8-10 different nucleic acid molecules or genes are targeted by the disclosed methods. In some examples, the disclosed methods are used to treat or prevent a disease associated with non-expression or reduced expression (e.g., at least 10%, at least 20%, at least 30%, at least 40%, at least 50%, at least 60%, at least 70%, at least 80%, at least 90%, at least 95%, at least 99%, or 100% reduction) of one or more genes. In one example, the target is associated with a disease such as type I diabetes, Duchenne muscular dystrophy, or acute kidney disease. In some examples, the disease is a disease of the liver, muscle, pancreas, or kidney. In some examples, the disease is liver disease such as Alagille syndrome; alpha-1 antitrypsin deficiency (alpha-1); biliary atresia; liver cirrhosis; galactosemia; Gilbert's syndrome; hemochromatosis; lysosomal acid lipase deficiency (LAL-D); non-alcoholic fatty liver disease (NAFLD); primary biliary cholangitis (PBC); primary sclerosing cholangitis (PSC); glycogen storage disease type I (GSD I); and Wilson's disease. In some examples, the gene or gene product that is targeted (e.g., activated) is one or more of Fst, Pdx1, Klotho, utrophin, interleukin 10, insulin 1, insulin 2, Pcsk1, Six2, Foxa3, Gata4, HNF1a and HNF4a. In a specific, non-limiting example, the disease is muscular dystrophy, the causative gene is dystrophin, and the target gene is utrophin.In another non-limiting example, the disease is a liver disease, such as liver fibrosis and / or cirrhosis, and the target genes are Foxa3, Gata4, HNF1a and / or HNF4a.

[0219] Specific examples of genes that can be targeted (e.g., activated) with the disclosed methods and diseases that can be treated are provided in Tables 1 and 2. In certain embodiments, the targeting sequence is complementary to a sequence that is within at least about 10 nt, about 25 nt, about 50 nt, about 60 nt, about 70 nt, about 80 nt, about 90 nt, about 100 nt, about 110 nt, about 120 nt, about 130 nt, about 140 nt, about 150 nt, about 175 nt, about 200 nt, about 300 nt, about 400 nt, or about 500 nt of the transcription start site of the target gene.

[0220] VI. Reporter Disclosed herein are systems, kits and methods for measuring gene activation, such as when Cas9 (e.g., Cas9 or dCas9) is expressed or has a Cas9 expression step.The systems, kits and methods for measuring gene activation herein can be used to, for example, assay the efficiency of gene activation (e.g., the efficiency of gene activation by the mTGA system disclosed herein) and / or cell isolation or sorting (e.g., cell isolation or sorting with gene activation, or cell isolation or sorting without gene activation).

[0221] Systems and kits are provided herein for measuring gene activation when Cas9 is expressed. In some examples, the systems and kits include at least one gene activation vector and at least one reporter vector. Cas9 or Cas9, including dCas9, can be expressed constitutively or inducibly, and endogenously or exogenously, using any suitable method, kit, system, or composition, including the methods, kits, systems, and compositions disclosed herein, such as using a vector (e.g., a viral vector, e.g., an AAV vector) encoding Cas9 (e.g., Cas9 or dCas9). In some examples, at least one gene activation vector includes multiple crRNAs or multiple sgRNAs and at least one transcription activator protein. In some examples, at least one reporter vector includes target sequences of multiple crRNAs or multiple sgRNAs and at least one reporter protein, where the reporter protein is located downstream of the target sequence.

[0222] In some examples, the method includes injecting at least one gene activation vector and at least one reporter vector into a subject.Any suitable injection method can be used, including subcutaneous, intramuscular, intravenous, intraperitoneal, intracardiac, intraarticular, liver or its vasculature injection, and / or intracavity injection of any amount of at least one gene activation vector and at least one reporter vector (e.g., an effective amount of the vector as described herein).

[0223] The vector of at least one gene activation vector or at least one reporter vector can be any suitable vector, for example, any vector described herein. In some examples, the vector is a viral vector or a plasmid (e.g., a retrovirus, a lentivirus, an adenovirus, an adeno-associated virus, or a herpes simplex virus). In certain examples, the vector is an AAV vector (e.g., an AAV9 vector). In some examples, the AAV vector has a tropism for a specific tissue or cell type. In some examples, the guide nucleic acid molecule is operably linked to a promoter or an expression control element (examples of which are provided elsewhere in this application). In certain examples, the promoter is a minimal promoter such as cytomegalovirus (CMV), human b-actin (hACTB), human elongation factor-1a (hEF1a) and cytomegalovirus early enhancer / chicken b-actin (CAG) promoter (e.g., promoters described in Papadakis et al., Current Gene Therapy, 4:89-113, 2004; Damdindorj et al., PLoS ONE 9(8):e106472, 2014, both of which are incorporated by reference in their entirety). The vector may contain other elements, such as a gene encoding a selection marker, such as an antibiotic, such as puromycin or hygromycin, or a detectable marker, such as GFP, another fluorophore, or luciferase protein. Such vectors may contain naturally occurring or non-naturally occurring nucleotides or ribonucleotides. Such vectors may be used in the methods, compositions and kits provided herein.

[0224] At least one reporter vector may include at least one reporter protein located downstream of the target sequence. Any suitable reporter protein can be used, such as a fluorescent protein, a bioluminescent protein, or any combination thereof. Exemplary reporter proteins include infrared fluorescent protein (IFP), mRFP1, mCherry, mOrange, DsRed, dTomato (or tdTomato), mKO, tagRFP, EGFP, mEGFP, mOrange2, maple, tagRFP-T, firefly luciferase, Renilla luciferase, and click beetle luciferase (e.g., U.S. Patent Application Publication No. 2010 / 0122355, the entirety of which is incorporated herein by reference). In some examples, the at least one reporter protein can include about 1, about 2, about 3, about 4, or about 5 reporter proteins. In further examples, the at least one reporter protein can include about 1-5, about 1-4, about 1-3, about 1-2, about 2-5, about 3-5, about 4-5, or about 2-4 reporter proteins. In particular examples, the at least one reporter protein includes luciferase, mCherry, dTomato, or any combination thereof (e.g., a combination of luciferase and mCherry or a combination of luciferase and dTomato). The target sequence can be any target sequence of interest that is complementary to the crRNA or modified sgRNA (including dgRNA) of the gene activation vector.

[0225] At least one gene activation vector comprises at least one multiple crRNA or multiple sgRNA and at least one transcription activator protein.Multiple crRNAs and multiple sgRNAs are disclosed herein.Transcription activator proteins, such as VP64, P65, MyoD1, HSF1, RTA, SET7 / 9, or any combination thereof, are also described herein.In a specific, non-limiting example, at least one transcription protein comprises P65 and HSF1 (e.g., SEQ ID NO: 35). EXAMPLES

[0226] Example 1 material and method mouse Gt(ROSA)26Sor tm1.1(CAG-cas9*,-EGFP)Fezh / J (herein Rosa26-Cas9 knock-in or post-Rosa26-Cas9; stock no. 024858) and C57BL / 10ScSn-Dmd mdx / J (herein Mdx post-J; stock number 001801) mice were obtained from Jackson Laboratory. Rosa26-Cas9 mice were crossed with Mdx mice to express Cas9 + / - Mdx + / - We generated mice with Cas9 + / - Mdx + / - Mice were bred to generate Cas9Mdx mice. Both male and female mice aged 6 weeks to 4 months were used for this study.

[0227] Plasmid design and construction The sequence of MS2-P65-HSF1 (MPH) was cloned from the plasmid lenti_MS2-P65-HSF1_Hygro (Addgene 61426). The sequences of Spc5.12 promoter and CW3SL were directly synthesized by Gene Universal®. EF1-MPH-CW3SL and Spc-MPH-CW3SL vectors were constructed by subcloning EF1 or Spc5.12 promoter, MPH and CW3SL into the AAV backbone using In-Fusion® cloning (Takara Bio). mTGA constructs were synthesized by Gene Universal®. The mTGA constructs were inserted into the EF1-MPH-CW3SL and Spc-MPH-CW3SL vectors by the In-Fusion® cloning method to generate UtrnTriple AAV or UtrnTriple-crRNA AAV vectors. An AAV dCas9 vector (AAV-Spc-dCas9) was constructed by replacing the nEF promoter of AAV-nEF-Cas9 (Liao, et al. (2017) Cell 171:1495-1507 e1415) with the Spc5.12 promoter.

[0228] AAV production AAV-DJ or AAV-Cas9 (AAV2 inverted terminal repeat (ITR) vector pseudotyped with AAV-DJ or AAV9 capsid) viral particles were generated according to the Gene Transfer Targeting and Therapeutics Core procedures at the Salk Institute for Biological Studies. Briefly, AAVpro HEK293T cells were maintained in 15 cm Petri dishes containing 20 ml of complete DMEM (+10% FBS, GlutaMAX (100x), NEAA (100x)) with 30 plates for high titer preparation. Cells were approximately 70% confluent for transfection. HEK293 cells were transiently transfected using the polyethylenimine transfection method. Cells were harvested 72 hours after transfection and virus was released into the supernatant after three cycles of freeze-thaw. Virus was purified using CsCl gradient centrifugation followed by dialysis against two cycles of PBS and one cycle of 5% sorbitol-PBS. The virus was then concentrated using an Amicon® Ultra-4 Centrifugal Filter Unit (Ultracel®-100K).

[0229] Intramuscular injection of AAV and collection and excision of tibialis anterior muscle Mice were anesthetized using an intraperitoneal injection of ketamine (100 mg / kg) and xylazine (10 mg / kg). Tibialis anterior (TA) muscles were collected and embedded in Tissue-Tek OCT compound for cryosectioning according to the protocol of Wang and Kuang (Bio-Protocol 7:e2279, 2017). 10 μm thick sections were collected on positively charged microscope slides at room temperature. These slides were further processed for immunostaining.

[0230] Immunostaining of muscle sections Muscle sections were fixed with 4% paraformaldehyde. After washing with PBS and glycine, sections were blocked with blocking buffer (5% goat serum, 2% BSA, 0.2% triton® X-100 and 0.1% sodium azide in PBS) for at least 30 min. Anti-utrophin (sc-15377 from Santa Cruz Biotechnology®) was diluted 200-fold in blocking buffer, and sections were incubated with primary antibody at 4°C overnight. The next day, after washing with PBS, samples were incubated with donkey anti-rabbit IgG (H+L) (Alexa Fluor® 488, A-21206) and DAPI for 45 min at room temperature. Immunostaining images were captured using a Zeiss® LSM 710 laser scanning confocal microscope.

[0231] RNA extraction and real-time qPCR Total RNA of muscles and myoblasts was extracted using Trizol® Reagent (Ambion®). Muscles and myofibers were homogenized using an EpiShear™ Probe Sonicator. RNA was treated with RNase-free DNase I to remove genomic DNA. Purity and concentration of total RNA were measured by Synergy™ H1 (BioTek®). cDNA was generated by reverse transcription using Maxima H Minus Reverse Transcriptase (ThermoFisher Scientific). qPCR analysis was performed on a CFX 384 Real-Time System (Bio-Rad) using SsoAdvanced™ Universal SYBR® Green Supermix (Bio-Rad). Expression levels of each gene were normalized to the housekeeping gene GADPH. Primer sequences were the same as in Liao, et al. (Cell 171:1495-1507 e1415,2017).

[0232] RNA-seq analysis Total RNA of isolated cells was collected using the TRIzol® method. RNA quality and quantity were assessed using Agilent 2200 TapeStation™ and Invitrogen® Qubit®. RNA-Seq libraries were constructed using Illumina® Smart-Seq2® with Nextera® XT DNA Library Prep kit, and 2 × 150 bp paired-end sequencing was performed on an Illumina® HiSeq X™ Ten system. Raw reads were aligned to the mm10 genome using STAR [v2.5.3a] with default parameters. The number of reads was then uniquely aligned to RefSeq (available from the National Center for Biotechnology Information (NCBI)), and exons were quantified by HOMER [v4.9.1].

[0233] Protein extraction and Western blot analysis Muscle samples were washed with PBS and homogenized in radioimmunoprecipitation assay buffer (50 mM Tris-HCl (pH 8.0), 150 mM NaCl, 1% NP-40, 0.5% sodium deoxycholate, and 0.1% SDS). Proteins (100ug) were separated by 3-8% Criterion™ Tris-Acetate protein gel (Bio-Rad), electrotransferred to PVDF membrane (Millipore), and incubated with specific primary antibodies. Anti-utrophin (sc-15377 from Santa Cruz Biotechnology®) and anti-Gapdh (2188S from Cell Signaling) were diluted in 5% w / v nonfat dry milk at a ratio of 1:1000. Immunodetection was performed using SuperSignal™ West Pico PLUS Chemiluminescent Substrate (Thermo Scientific).

[0234] statistical analysis Data presented were obtained from separate samples with mean and standard deviation (SD). P values ​​were calculated using a two-tailed unpaired Student's t-test. All analyses were performed using Prism 7 software. A P value of less than 0.05 was considered statistically significant.

[0235] Example 2 Development of a multiplex TGA (mTGA) system with two dgRNAs dgRNAs targeting different regions of the utrophin locus were screened for utrophin activation. One gRNA (dgUtrnNT2, SEQ ID NO: 12) was observed to outperform dgUtrnT2 and dgUtrnT16, which were the most efficient gRNAs in the original screen (Figure 5). The combination of gRNA and MPH was compared with N2a Cas9 To determine whether synergistic effects could be achieved by transfecting cells, dgUtrnNT2, dgUtrnT2 and dgUtrnT16 were selected for further testing. When multiplexed dgRNAs were utilized, utrophin activation was enhanced without increasing the total dgRNA concentration. The mixture of three dgRNAs (SEQ ID NO: 12, 14 and 15) showed the strongest synergistic effect, with an 18-fold upregulation (7-fold higher than using a single dgRNA) (Figure 6A).

[0236] Eukaryotic translation elongation factor 1 alpha 2 (Eef1a2) is responsible for the translation of utrophin. We identified an efficient dgRNA to induce the expression of Eef1a2 (Figure 6B) and investigated whether the duplex of Eef1a2 and utrophin dgRNA could enhance the protein level of utrophin by simultaneously enhancing transcription and translation. dgEef1a2 (dgRNAT2) is a dgRNA that expresses N2a Cas9 dgEef1a2 and dgUtrnNT2 duplex significantly enhanced utrophin upregulation by 3.7-fold in cells (Figure 7). These results indicate that multiplexed gRNAs can enhance the efficiency of the TGA system.

[0237] Based on these findings, an mTGA system containing multiple utrophin and / or Eef1a2 dgRNAs and the MPH activation complex was developed in a single AAV vector for in vivo application. Multiple modifications were made to develop the mTGA system. For example, to create space for inserting additional dgRNAs in the same AAV vector, the expression of the MPH transcription activation complex is driven by a shorter promoter. The original CAG promoter was replaced with either a ubiquitous promoter (EF1a) or a muscle-specific promoter (Spc5.12) (Figure 8). The WPRE-pA cassette was replaced with a shorter but equally efficient element, CW3SL (Choi et al., Molecular brain, 7:17, 2014). In addition, deleterious recombination events, such as truncation and rearrangements, are often observed in AAV vectors containing multiple repeat fragments. Recombination can dramatically reduce the efficiency of AAV and cause by-products with undesired rearrangements. The two main sources of repeat sequences are derived from the dgRNAs, their respective promoters. To address undesired recombination, different RNA polymerase III promoters (hU6, mU6, and H1) were first used to drive the expression of different sgRNAs. hU6 and mU6 had approximately two-fold higher activation efficiency than H1 (Figure 9; see also Figure 10), and therefore hU6 and mU6 were selected for the mTGA system containing two sgRNAs.

[0238] The activities of two mTGA systems containing two sgRNAs (in different orientations) were compared. The activity of targeted gene induction by the mTGA system with inverted repeats (one sgRNA in forward orientation, one sgRNA in reverse orientation) was found to be higher than that of the mTGA system with direct repeats (both sgRNAs in forward orientation) (see also Figure 11, Figure 14). It was also observed that the mTGA system with two sgRNAs in forward orientation was prone to undesired recombination, whereas such recombination did not occur in the mTGA system with inverted repeats (see also Figure 12 and Figure 13, Figure 15). The results demonstrate that undesired recombination of duo-dgRNA can be reduced by the inverted repeat orientation.

[0239] Example 3 Duo mTGA System in vivo A skeletal muscle-specific duplex TGA system was designed in which duo-dgRNA is oriented under an inverted repeat with the MPH complex driven by the muscle-specific promoter Spc5.12 (Figure 16). The duplex TGA system was transfected into the tibialis anterior (TA) muscle of Cas9 / mdx mice at 1x10 11 GCs AAV9-dgUtrnT2-dgFst-MPH, AAV9-dgUtrnNT2-dgEef1a2-MPH or AAV9-MPH were applied in vivo by intramuscular injection. dgUtrnT2 and follistatin (Fst) dgRNA were applied individually to increase utrophin expression and induce muscle hypertrophy, respectively (Liao et al., Cell 171:1495-1507, e1415, 2017). The duplex effect of dgUtrnT2 / dgFst and dgUtrnNT2 / dgEef1a2 on the vulnerability of mdx muscles, which are susceptible to contraction-induced injury, was investigated. AAV injection (1 × 10 11 Sarcolemma integrity was monitored 8 weeks after GC with an Evans Blue dye (EBD) assay. Damaged muscle fibers accumulate EBD and produce red fluorescence.

[0240] Extensive EBD uptake was observed in TA muscles injected with AAV9-MPH and AAV9-dgUtrnT2-dgFst-MPH (Figure 17). In contrast, EBD uptake was significantly reduced in muscles treated with AAV9-dgUtrnNT2-dgEef1a2-MPH. Although AAV9-dgUtrnT2-dgFst-MPH treatment induced muscle hypertrophy, the increase in muscle mass did not prevent muscle fragility (Figure 17). Next, we examined the expression of the targeted genes. AAV9-dgUtrnT2-dgFst-MPH treatment increased the expression of utrophin and Fst by 1.8-fold and 10-fold, respectively (Figure 18A). AAV9-dgUtrnNT2-dgEef1a2-MPH treatment increased the expression of utrophin and Eef1a2 by 2.6-fold and 2.2-fold, respectively (Figure 18B). The protein level of utrophin was also measured. After AAV9-dgUtrnT2-dgFst-MPH treatment, utrophin expression was upregulated 1.5-fold. In contrast, AAV9-dgUtrnNT2-dgEef1a2-MPH treatment enhanced utrophin expression 3.7-fold (Figure 19). Immunostaining revealed stronger utrophin signals in myofiber sarcomas treated with AAV9-dgUtrnNT2-dgEef1a2-MPH than AAV9-dgUtrnT2-dgFst-MPH or AAV9-MPH (Figure 20). The results indicate that the duplex mTGA system works efficiently in vivo to induce phenotypic changes. Furthermore, it is shown that this system can be designed to enhance utrophin expression to help prevent myofiber fragility.

[0241] Example 4 Development of an mTGA system with three dgRNAs Although the use of two different RNA polymerase III promoters in inverted orientation helped to reduce recombination when using two dgRNAs in the same AAV vector, additional challenges were faced when adding a third sgRNA. As shown in Figures 21 and 22, the addition of a third sgRNA, with a direct repeat to one of the previously inverted sgRNAs, causes significant truncation and induces undesired loss of the dgRNA.

[0242] To address this issue, we incorporated an additional sgRNA using a technique that exploits the endogenous tRNA processing system. We found that the activity of the sgRNA (dgFst) following the tRNA was approximately half that of the inverted construct containing dgFst driven directly by hU6 (Figure 23).

[0243] The hU6-dgUtrnNT2-tRNA-dgFst construct was also compared with the hU6-dgUtrnNT2-H1-dgFst construct in which the third gRNA is driven by the H1 promoter (Figure 24). Due to the incomplete processing and maturation of gRNA from the tRNA-gRNA transcript (Xu et al., Science advances 3:e1602814,2017), the activation efficiency of the gRNA upstream of the tRNA (dgUtrnNT2) and the gRNA downstream of the tRNA (dgFst) was 10% and 44% lower, respectively, than those directly driven by hU6. There was no significant difference between the gRNA in the hU6-dgUtrnNT2-tRNA-dgFst construct and the gRNA in the hU6-dgUtrnNT2-H1-dgFst construct by non-viral plasmid transfection.

[0244] Considering that the third sgRNA needed to be driven by the H1 promoter (to avoid recombination), which also showed half the activation efficiency compared to the mU6 and hU6 promoters, the reduction in sgRNA activity after tRNA was tolerable. A construct with a single promoter driving the expression of two sgRNAs separated by a tRNA reduced deleterious recombination events when the two sgRNAs were both in the forward orientation (Figure 25). In this way, an mTGA system containing three sgRNAs was constructed.

[0245] AAV containing hU6-tRNA or hU6-H1 constructs was added at 1x10 10 C2C12 with genome copies (GC) of AAVDJ-hU6-dgUtrnNT2-tRNA-dgFst-MPH, AAVDJ-hU6-dgUtrnNT2-H1-dgFst-MPH or AAVDJ-MPH Cas9 The activation efficiency of dgUtrnNT2 was comparable between the hU6-tRNA and hU6-H1 constructs, while dgFst had a 2.2-fold higher activation efficiency in the hU6-tRNA construct compared to the hU6-H1 construct (Figure 26). There were fewer deleterious recombination events in the hU6-tRNA construct than in the hU6-H1 construct (Figure 27). Then, C2C12 Cas9 The ratio of tRNA or H1 to hU6 in the plasmid and AAV recovered from the cells was quantified using qPCR. Because tRNA or H1 was removed after recombination, the ratio reflects the recombination events that occurred during AAV production and infection. The ratio of tRNA to hU6 in AAV was 51% of that in the plasmid, while the ratio of H1 to hU6 in AAV was 22% of that in the plasmid, indicating that 59% (78% vs. 49%) more recombination events occurred in the hU6-H1 construct compared to the hU6-tRNA construct (Figure 28). Based on these observations, an mTGA system was constructed containing three gRNAs targeting MyoD, Mef2b, and Pax7. 3T3L1 Cas9 Efficient activation of MyoD, Mef2b and Pax7 in 1 × 10 cells containing only MPH 10reported after processing of the AAVDJ or mTGA systems (Figure 29).

[0246] We developed an mTGA system containing a combination of three tandem utrophin-targeting sgRNAs (UtrnTriple) and expressed N2 Cas9 or C2C12 using non-viral transfection in cells Cas9 Tested in vitro using AAV (serotype DJ) transfection into myoblasts. Controls included AAV vectors with a single utrophin dgRNA and MPH (UtrnT2), or MPH alone. Activation of utrophin was higher using mTGA compared to either control (MPH alone or single dgRNA TGA system) (Figure 30).

[0247] It was also confirmed that the mTGA system containing three dgRNAs activated the expression of multiple target genes in the tibialis anterior (TA) muscles of Cas9+Mdx mice (Figure 31).

[0248] Example 5 Development of an mTGA system with four dgRNAs The mTGA system was expanded to contain four gRNAs. The third and fourth gRNAs were driven by mU6 and hU6 after tRNA processing (Figure 32). Two different tRNAs (from yeast and maize) were selected to minimize repetitive sequences (Xie et al., PNAS, 112:3570-3575, 2015; Zhang et al., Nature Communications, 10:1053, 2019). The mTGA system was used to synthesize 1 × 10 GFP containing only MPH or the mTGA system. 10 AAVDJ processing results in BJ Cas9 The AAV-mediated mTGA system activated the expression of OCT4, SOX2, KLF4 and c-MYC in cells (Figure 32). The results indicate that the AAV-mediated mTGA system works efficiently to activate at least four genes.

[0249] Example 6 In vivo UtrnTriple mTGA system The mTGA system was administered using 2 × 10 GFP-containing MPH only (AAV-MPH), TGA system (single utrophin sgRNA, AAV-UtrnT2, see U.S. Patent Application Publication No. US-2021-0102206-A1) or mTGA system (triple utrophin sgRNA, AAV-UtrnTriple). 11 The expression of utrophin was tested in vivo by intramuscular injection of vg AAV (serotype 9) into the TA muscle of Cas9-expressing mice. Two months after AAV injection, utrophin expression increased up to 24-fold (average 16-fold) in muscles injected with the mTGA system (Figure 33A). In contrast, the average level of increase was only 2.5-fold for the original TGA system (UtrnT2). RNA-seq analysis was also performed for an unbiased analysis of utrophin expression. The norm read of utrophin was about 16-fold higher in muscles treated with the mTGA system compared to MPH alone (Figure 33B). It was also confirmed that the level of utrophin protein was higher when using the mTGA system (Figure 34A). Immunostaining using an antibody against utrophin showed increased sarcolemmal localization in UtrnTriple-treated muscles compared to UtrnT2-treated TA muscles (Figure 34B).

[0250] The new mTGA system was administered intravenously via 2 × 10 transfection into the TA and gastrocnemius (GA) muscles of Cas9 / Mdx mice. 11The mice were further tested in vivo by intramuscular injection of vg of AAV-MPH, AAV-UtrnT2 or AAV-UtrnTriple. Grip strength and Evans Blue Dye (EBD) uptake were assessed 2 months after AAV injection. Grip strength tests were repeated 60 times consecutively for each mouse. Readings for every 10 trials were averaged. Grip strength of Cas9 mice was found to be constant in consecutive trials. In contrast, grip strength of Mdx / Cas9 mice and Mdx mice decreased in a linear regression pattern with a slope of approximately -10 (Figure 35). TGA treatment delayed the decreasing trend with a slope of -5, whereas mTGA treatment rescued the decrease in grip strength (Figure 35). Sarcolemma integrity was also monitored by the uptake of EBD, which accumulates in damaged cells. The data show extensive EBD uptake in Mdx mice with AAV-MPH and AAV-UtrnT2 injections (Figure 36). In contrast, EBD uptake is greatly reduced in AAV-UtrnTriple-treated mice (Figure 36). We also measured utrophin expression in TA muscles with one utrophin gRNA or multiple utrophin gRNAs. There was significant activation of utrophin in mTGA-treated mice compared to other samples (Figures 37 and 38).

[0251] mTGA system, 1×10 11The dual AAV system was used to test GC in wild-type (WT) mdx mice by injecting AAV9-dCas9 and AAV9-UtrnTriple into the TA muscle of one side of the mouse (Figure 39). The contralateral TA muscle control was injected with AAV9-dCas9 and AAV9-MPH. Sarcolemma integrity was assessed by EBD uptake 2 months after treatment (Figure 39). Extensive EBD uptake was seen in the control treatment. In contrast, EBD uptake is significantly alleviated by mTGA treatment. Immunostaining also confirmed efficient activation of utrophin (Figure 39). Utrophin expression was quantified by qPCR and Western blot. Compared to the control leg, utrophin mRNA levels were increased 4.6-fold in TA muscles treated with the mTGA system (Figure 40A). Western blot showed that Utrn protein levels were significantly elevated 4-fold (Figure 40B). Thus, the disclosed mTGA system can be utilized as a treatment for DMD.

[0252] Example 7 Multiplexed gRNAs synergistically enhance epigenetic modifications The TGA system can modify histone modifications near targeted genomic loci (Liao et al., Cell 171:1495-1507, e1415, 2017). To identify histone modifications after mTGA treatment, TA muscles of Cas9 / mdx mice were inoculated with 1 × 10 11 GCs were injected with AAV9-MPH, AAV9-hU6-dgUtrnT2-MPH, AAV9-UtrnDual, or AAV9-UtrnTriple (Figure 41A). Utrophin mRNA levels were only slightly increased by dgUtrnT2 2 months after AAV injection (Figure 41B). In contrast, the levels were increased 4-fold by AAV9-UtrnDual and 5.5-fold by AAV9-UtrnTriple.

[0253] Chromatin immunoprecipitation (ChIP) qRT-PCR of TA muscle samples was performed. H3K4me3 and H3K27ac epigenetic marks, typically associated with transcriptionally active genes, were enriched at the target locus in AAV9-hU6-dgUtrnT2-MPH injected mice compared to AAV9-MPH controls (Figure 42 and Figure 43). Interestingly, AAV9-UtrnDual and AAV9-UtrnTriple not only enhanced the enrichment of H3K4me3 and H3K27ac marks but also extended the epigenetic changes compared to AAV9-hU6-dgUtrnT2-MPH. AAV9-UtrnTriple further altered epigenetic marks near UtrnT16 compared to AAV9-UtrnDual. The data indicate that the mTGA system synergistically enhances epigenetic changes around the target site.

[0254] Example 8 Sustained utrophin activation induced by the mTGA system Although the mTGA system induced strong epigenetic changes, it was unclear whether long-term gene activation could be achieved with short-term expression of the system. To investigate, a mouse line (idCas9) carrying tetO-driven dCas9 + reverse tetracycline transactivator (rtTA) was generated, allowing the regulation of dCas9 expression by doxycycline (Dox) administration (Figure 44A). The TA muscle of idCas9 mice was co-injected with AAV containing a luciferase reporter in which luciferase was placed downstream of the dgRNA (dgLuc) binding site and AAV containing the dgLuc-CAG-MPH sequence. Dox water (1 mg / ml) was then added and removed at 1- or 2-week intervals. The luciferase signal was significantly induced 1 week after Dox administration and returned to basal levels 2 weeks after Dox removal (Figure 44B). Since dCas9 was required for luciferase activation, the data demonstrate that expression of dCas9 was regulated by Dox administration in idCas9 mice. 11We investigated the endogenous activation of utrophin in idCas9 mice injected with GC AAV9-UtrnTriple or AAV9-MPH. Utrophin expression was increased approximately 8-fold after 30 or 60 days of continuous Dox administration (Figure 45). In contrast, no overexpression of utrophin was observed after 30 days of Dox withdrawal. These data demonstrate that the mTGA system is required for gene activation.

[0255] Sustained transgene expression has been reported in human skeletal muscle 10 years after injection of AAV carrying the transgene (Buchlis et al., Blood 119:3038-3041, 2012). To follow up on the persistence of the AAV-mediated mTGA system, 1 × 10 11 GCs were co-injected with AAV9-dCas9 and AAV9-UtrnTriple or AAV9-MPH (Figure 46A). Muscle samples were collected 13 months later, and a three-fold increase in utrophin was seen in samples treated with the mTGA system (Figure 46B). Immunostaining confirmed efficient activation of utrophin (Figure 46C). H&E and Mallory-Trichrome staining were utilized to evaluate the histopathological phenotype of mdx muscles. H&E staining showed that muscle interstitial spaces were larger and myofiber size was smaller in control treatment compared to mTGA treatment (Figure 47A). Furthermore, Mallory-Trichrome staining showed that mTGA-treated muscles had less fibrosis compared to control muscles (Figure 47B). Thus, the AAV-mediated mTGA system has a long-lasting effect on gene activation and pathological phenotype improvement.

[0256] Example 9 Enhancement of mTGA efficiency by optimizing gRNA combinations We optimized gRNA combinations to enhance utrophin expression. Because dgUtrnNT2-dgUtrnT2 (UtrnDual) and dgUtrnNT2-dgUtrnT2-dgUtrnT16 (UtrnTriple) similarly altered histone modifications in the utrophin promoter, we generated AAV9-UtrnDual-Eef1a2 to simultaneously enhance utrophin transcription and translation and compared it with AAV9-UtrnTriple and AAV9-UtrnNT2-Eef1a2 (Figure 48). Dual AAV injections (1x10 11 Two months after GC, AAV9-UtrnDual-Eef1a2 / AAV9-dCas9 treatment increased Eef1a2 expression by 2.2-fold and utrophin expression by 3.5-fold (Figure 49A). In contrast, AAV9-UtrnNT2-Eef1a2 / AAV9-dCas9 increased Eef1a2 and utrophin expression by 1.9-fold and 2-fold, respectively, and AAV9-UtrnTriple / AAV9-dCas9 upregulated utrophin expression by 4.9-fold without changing Eef1a2 expression (Figure 49A). Interestingly, AAV9-UtrnDual-Eef1a2 / AAV9-dCas9 treatment enhanced utrophin protein by 5.3-fold and improved utrophin protein upregulation by 27% compared to AAV9-UtrnNT2-Eef1a2 / AAV9-dCas9 and AAV9-UtrnTriple / AAV9-dCas9 treatments (Figure 49B).

[0257] The optimized mTGA system containing AAV9-UtrnDual-Eef1a2 and AAV9-dCas9 was also used to treat adult mdx mice. Systemic treatment by tail vein injection was examined, but the use of a luciferase reporter (AAV9-Spc5.12-Luc) to track the distribution of AAV after tail vein injection revealed that AAV did not efficiently enter muscle cells even at high AAV titers (1 × 10 12 GC; Figure 57). Therefore, instead of using tail vein injections, we injected the TA muscle (1 × 10 11 GC), GA muscle (2 × 1011 GC), quadriceps (2×10 11 GC), deltoid muscle (5×10 10 GC), triceps (5×10 10 GC), trapezius muscle (1×10 11 Intramuscular injection of the dual AAV system into multiple muscles of 2-month-old mdx mice (at titers according to muscle size) containing AAV9-MPH / AAV9-dCas9 (Figure 50A). Two months after AAV treatment, serum creatine kinase activity was reduced 3-fold in mice treated with the mTGA system compared to mice treated with AAV9-MPH / AAV9-dCas9 (Figure 50B). In the open field test, control mdx mice jumped less and had longer resting times compared to WT mice. mTGA treatment rescued the reduced activity of mdx mice (Figure 51A). Treadmill testing also revealed that mTGA treatment improved the speed and endurance of treated mdx mice compared to control mdx mice (Figure 51B).

[0258] Example 10 Development of multiplex crRNA mTGA constructs The disclosed mTGA system was further optimized to reduce recombination of promoter-tRNA constructs. Recombination events were monitored by generating hU6-tRNA constructs containing gRNAs with different backbones (Figure 52). After sequencing the truncated bands of the hU6-tRNA constructs, recombination was found to occur between the first and fourth MS2 loops (each gRNA contains two MS2 loops), reducing the four MS2 loops to two. We hypothesized that recombination could be minimized if the repetitive dgRNA scaffold was reduced. Since gRNAs can be split into crisper RNA (crRNA) and trans-activating crisper RNA (tracrRNA) elements, a single tracrRNA can be used with multiple crRNAs for multiplexing purposes. To test this, we split the dgRNA into a CRISPR RNA (crRNA) and a modified trans-activating CRISPR RNA (tracrRNA-M2) containing two MS2 loops, and linked the polycistronic system with tRNA (Figure 53A). The crRNA-tRNA-tracrRNA-M2 construct activated the target gene, but its activation efficiency was 2.8-fold lower than dgRNA. Its activation efficiency was also compared using tRNAs from different species. tRNAs from yeast and maize were 5-fold more efficient compared to tRNAs from flies (Figure 53A). We then investigated whether a single tracrRNA-M2 could be used with two crRNAs to activate the corresponding targets. Interestingly, when the two crRNAs were driven by two different U6 promoters, only the crRNAs that shared the same promoter as tracrRNA-M2 had strong activation efficiency (Figure 53B). Therefore, a single promoter driving tracrRNA-M2 and two crRNAs (separated by different combinations of self-cleaving RNAs) was developed (see Figure 54). The activation efficiency of different constructs was compared using N2 Cas9 Tested in vitro using non-viral transfection in cells, the best construct was determined to be the one with tracrRNA-M2 preceding two crRNAs linked by tRNA and HDV-HH (Figure 54). The sgRNA following the second tRNA was found to have low activation efficiency in the construct with two tRNAs (Figure 54). Interestingly, the recombination found to occur in the construct with one promoter and two sgRNAs separated by tRNA was eliminated from the construct containing one promoter driving the expression of tracrRNA-M2 and two crRNAs (Figure 55). However, the activation efficiency of AAVDJ-hU6-tracrRNA-M2-tRNA-crFst-HDV-HH-crUtrn-MPH was not higher than that of AAVDJ-hU6-dgUtrnT2-tRNA-dgFst-MPH (Figure 56A).

[0259] Example 11 In vivo multiplex crRNA mTGA system In vivo activation of utrophin was compared between UtrnTriple, in which two gRNAs are driven by hU6-tRNA constructs, and UtrnTriple-crRNA, in which two gRNAs are driven by tracrRNA-crRNA constructs (Figure 56B). Two months after intramuscular injection of different concentrations of AAV9-MPH, AAV9-UtrnTriple, or AAV9-UtrnTriple-crRNA into the TA muscle of Cas9 / mdx mice, AAV9-UtrnTriple increased utrophin activation by 5×10 10 GC has a significantly higher activation efficiency than AAV9-UtrnTriple-crRNA, but at an AAV concentration of 1 × 10 11 The difference was found to be not significant over GC (Figure 56B). The data show that the efficiency of the mTGA system is AAV concentration dependent (Figure 56B).

[0260] Example 12 Treatment of Liver Disease This embodiment describes the method that can be used to treat liver fibrosis and / or cirrhosis in vivo.Although specific method is provided, those skilled in the art will recognize that methods that deviate from these specific methods can also be used, including adding or omitting one or more steps.

[0261] In this example, crRNAs and / or sgRNAs targeting one or more of HNF1a, HNF4a, FoxA3 and Gata4 are designed for use in the mTGA system described herein. CMV and / or Col1a2 promoters are used to drive expression of multiple crRNAs or sgRNAs. The mTGA constructs are cloned into an AAV vector, such as AAV9 (hereinafter referred to as AAV-mTGA).

[0262] Mice were injected with AAV-MPH (control) or AAV-mTGA. Activation efficiency is assessed using qPCR and Western blot analysis of the target genes. Mouse livers can also be harvested to determine whether fibrosis and / or cirrhosis is reduced following treatment.

[0263] In view of the many possible embodiments to which the principles of this disclosure may be applied, it should be recognized that the illustrated embodiments are merely examples of the invention and should not be construed as limiting the scope of the invention. Rather, the scope of the invention is defined by the following claims. We therefore claim as our invention all that comes within the scope and spirit of these claims.

Claims

1. A nucleic acid encoding multiple single guide RNAs (sgRNAs), comprising, from 5' to 3': a first nucleic acid molecule encoding a first modified sgRNA in a reverse orientation operably linked to a first promoter; a second nucleic acid molecule encoding a second modified sgRNA in a forward orientation operably linked to a second promoter; A nucleic acid, wherein the encoded first and second modified sgRNAs comprise at least two modified MS2 binding loops comprising at least two nucleotide changes relative to the native MS2 binding loop sequence of SEQ ID NO: 16, wherein the at least two nucleotide changes increase the GC content and / or shorten the repetitive content of the modified MS2 binding loop sequence compared to the native MS2 binding loop sequence.

2. a third nucleic acid molecule located 3' of the second nucleic acid molecule, the third nucleic acid encoding a first cleavage site and a third modified sgRNA in a forward orientation; 2. The nucleic acid of claim 1, wherein the third modified sgRNA is operably linked to the second promoter and comprises at least two modified MS2 binding loops comprising at least two nucleotide changes relative to the native MS2 binding loop sequence of SEQ ID NO: 16, wherein the at least two nucleotide changes increase the GC content and / or shorten the repetitive content of the modified MS2 binding loop sequence compared to the native MS2 binding loop sequence.

3. a third nucleic acid molecule located 5' of the first nucleic acid molecule, the third nucleic acid encoding a first cleavage site and a third modified sgRNA in a reverse orientation; 2. The nucleic acid of claim 1, wherein the third modified sgRNA is operably linked to the first promoter and comprises at least two modified MS2 binding loops comprising at least two nucleotide changes relative to the native MS2 binding loop sequence of SEQ ID NO: 16, wherein the at least two nucleotide changes increase the GC content and / or shorten the repetitive content of the modified MS2 binding loop sequence compared to the native MS2 binding loop sequence.

4. a fourth nucleic acid molecule located 5' of the first nucleic acid molecule, the fourth nucleic acid molecule encoding a second cleavage site and a fourth modified sgRNA in a reverse orientation; 3. The nucleic acid of claim 2, wherein the fourth modified sgRNA is operably linked to the first promoter and comprises at least two modified MS2 binding loops comprising at least two nucleotide changes relative to the native MS2 binding loop sequence of SEQ ID NO: 16, wherein the at least two nucleotide changes increase the GC content and / or shorten the repetitive content of the modified MS2 binding loop sequence compared to the native MS2 binding loop sequence.

5. 5. The nucleic acid of claim 4, wherein one or more of the first, second, third, or fourth modified sgRNA comprises SEQ ID NO: 17, 18, or 19.

6. 5. The nucleic acid of claim 4, wherein the first cleavage site, the second cleavage site, or both, encode a self-cleaving RNA.

7. The nucleic acid of claim 6 , wherein the self-cleaving RNA is a pre-transfer RNA (pre-tRNA) or a self-cleaving ribozyme.

8. 8. The nucleic acid of claim 7, wherein the first cleavage site encodes a pre-tRNA and the second cleavage site encodes a pre-tRNA from a different organism.

9. 5. The nucleic acid of claim 4, wherein one or more of the first, second, third or fourth modified sgRNA comprises a targeting sequence complementary to a sequence within the promoter region of EEF1α2, Fst, Pdx1, Klotho, utrophin, interleukin-10, Six2, OCT4, SOX2, KLF4, c-MYC, MyoD, Mef2b or Pax7.

10. 5. The nucleic acid of claim 4, wherein one or more of the first, second, third, or fourth modified sgRNA comprises a sequence having at least 90% sequence identity to, comprises, or consists of, any one of SEQ ID NOs: 10-15 or 42-48.

11. The first modified sgRNA sequence comprises: comprises a sequence having at least 90% sequence identity to SEQ ID NO: 10, 11, 12, 13, 14 or 15; comprising SEQ ID NO: 10, 11, 12, 13, 14 or 15; or The nucleic acid of claim 1, consisting of SEQ ID NO: 10, 11, 12, 13, 14 or 15.

12. The second modified sgRNA sequence comprises: comprises a sequence having at least 90% sequence identity to SEQ ID NO: 10, 11, 12, 13, 14 or 15; comprising SEQ ID NO: 10, 11, 12, 13, 14 or 15; or The nucleic acid of claim 1, consisting of SEQ ID NO: 10, 11, 12, 13, 14 or 15.

13. The third modified sgRNA sequence comprises: comprises a sequence having at least 90% sequence identity to SEQ ID NO: 10, 11, 12, 13, 14 or 15; comprising SEQ ID NO: 10, 11, 12, 13, 14 or 15; or The nucleic acid of claim 2, consisting of SEQ ID NO: 10, 11, 12, 13, 14 or 15.

14. The fourth modified sgRNA sequence comprises: comprises a sequence having at least 90% sequence identity to SEQ ID NO: 10, 11, 12, 13, 14 or 15; comprising SEQ ID NO: 10, 11, 12, 13, 14 or 15; or The nucleic acid of claim 4, consisting of SEQ ID NO: 10, 11, 12, 13, 14 or 15.

15. The nucleic acid molecule comprises a sequence having at least 90% sequence identity to SEQ ID NO: 3, 53 or 54; comprising SEQ ID NO: 3, 53 or 54; or The nucleic acid of claim 1, consisting of SEQ ID NO: 3, 53 or 54.

16. The nucleic acid molecule comprises a sequence having at least 90% sequence identity to SEQ ID NO: 4 or 5; comprising SEQ ID NO: 4 or 5; or The nucleic acid according to claim 2, consisting of SEQ ID NO: 4 or 5.

17. The nucleic acid molecule comprises a sequence having at least 90% sequence identity to SEQ ID NO:55; comprising SEQ ID NO:55; or The nucleic acid of claim 3, consisting of SEQ ID NO:

55.

18. The nucleic acid molecule comprises a sequence having at least 90% sequence identity to SEQ ID NO:6; comprises SEQ ID NO:6; or The nucleic acid of claim 4, consisting of SEQ ID NO:

6.

19. 5. The nucleic acid of claim 4, wherein one or more of the first, second, third, or fourth sgRNA is a dgRNA.

20. A nucleic acid molecule encoding multiple CRISPR RNAs (crRNAs), comprising, from 5' to 3': the nucleic acid molecule encoding a modified trans-activating CRISPR RNA (tracrRNA) comprises a first promoter operably linked to a nucleic acid molecule encoding a modified trans-activating CRISPR RNA (tracrRNA), a first cleavage site, a first nucleic acid molecule encoding the first crRNA, a second cleavage site, and a second nucleic acid molecule encoding the second crRNA; A nucleic acid molecule, wherein the encoded modified tracrRNA comprises at least two modified MS2 binding loops comprising at least two nucleotide changes relative to the native MS2 binding loop sequence of SEQ ID NO: 16, wherein the at least two nucleotide changes increase the GC content and / or shorten the repetitive content of the modified MS2 binding loop sequence compared to the native MS2 binding loop sequence.

21. 21. The nucleic acid of Claim 20, further comprising a second promoter operably linked to a third nucleic acid molecule encoding a third crRNA or a single guide RNA (sgRNA).

22. i. the second promoter and the third nucleic acid molecule are 3' of the second nucleic acid molecule encoding a second crRNA; or ii. the second promoter and the third nucleic acid molecule are in inverse orientation and are located 5' of the first promoter; 22. The nucleic acid of claim 21.

23. 21. The nucleic acid of claim 20, wherein the first or second cleavage site encodes a pre-transfer RNA (pre-tRNA) or a self-cleaving ribozyme.

24. 24. The nucleic acid of claim 23, wherein the first cleavage site encodes a pre-tRNA and the second cleavage site encodes a self-cleaving ribozyme.

25. The modified tracrRNA is comprises a sequence having at least 90% sequence identity to SEQ ID NO:7; comprises SEQ ID NO:7; or 21. The nucleic acid of claim 20 consisting of SEQ ID NO:

7.

26. 22. The nucleic acid of claim 21, wherein one or more of the first crRNA, the second crRNA, the third crRNA, or the sgRNA comprises a targeting sequence complementary to a sequence within the promoter region of EEF1α2, Fst, Pdx1, Klotho, utrophin, interleukin-10, Six2, OCT4, SOX2, KLF4, c-MYC, MyoD, Mef2b, or Pax7.

27. The first, second, or third crRNA is comprises a sequence having at least 90% sequence identity to SEQ ID NO: 8, 9, 49, 50, 51, or 52; comprising SEQ ID NO: 8, 9, 49, 50, 51, or 52; or 22. The nucleic acid of claim 21, consisting of SEQ ID NO: 8, 9, 49, 50, 51, or 52.

28. The sgRNA is comprises a sequence having at least 90% sequence identity to SEQ ID NO: 10, 11, 12, 13, 14, 15, 42, 43, 44, 45, 46, 47, or 48; comprising SEQ ID NO: 10, 11, 12, 13, 14, 15, 42, 43, 44, 45, 46, 47 or 48; or 22. The nucleic acid of claim 21, consisting of SEQ ID NO: 10, 11, 12, 13, 14, 15, 42, 43, 44, 45, 46, 47 or 48.

29. The nucleic acid molecule comprises a sequence having at least 90% sequence identity to SEQ ID NO: 1 or 2; comprising SEQ ID NO: 1 or 2; or 21. The nucleic acid of claim 20 consisting of SEQ ID NO: 1 or 2.

30. 22. The nucleic acid of claim 21 , wherein the sgRNA is a dead guide RNA (dgRNA).

31. An RNA molecule encoded by the nucleic acid molecule of any one of claims 1 to 30.

32. A viral vector comprising the nucleic acid of any one of claims 1 to 30.

33. A composition comprising the nucleic acid according to any one of claims 1 to 30 and a pharma- ceutically acceptable carrier.

34. A composition comprising the RNA molecule of claim 31 and a pharma- ceutically acceptable carrier.

35. A nucleic acid according to any one of claims 1 to 30, A nucleic acid encoding a Cas9 protein or a dead Cas9 (dCas9) protein, and / or a nucleic acid encoding an MS2 transcriptional activator fusion protein; Including the kit.

36. a) a first vector comprising a nucleic acid encoding Cas9 or dCas9; b) a second vector comprising a nucleic acid according to any one of claims 1 to 30 and a nucleic acid encoding an MS2 transcriptional activator fusion protein; A multiple targeted gene activation (mTGA) system comprising:

37. 1. A combination for use in a method of increasing expression of at least one gene product in a subject, the method comprising: a) a first vector comprising a nucleic acid encoding Cas9 or dCas9; b) administering to the subject a nucleic acid according to any one of claims 1 to 30, and a second vector comprising a nucleic acid encoding an MS2 transcriptional activator fusion protein; A combination, wherein said combination infects cells of said subject, thereby increasing expression of said at least one gene product in said infected cells.

38. The combination described in claim 37, wherein the method comprises treating a disease associated with reduced or non-expression of a gene.

39. 39. The combination of claim 38, wherein the disease is type I diabetes, Duchenne muscular dystrophy, liver disease or acute kidney disease.

40. 34. The composition of claim 33 for treating type I diabetes, Duchenne muscular dystrophy, liver disease or acute kidney disease in a subject.

41. (i) administering the composition increases expression of at least one gene target; or (ii) the subject is a human; 41. The composition of claim 40.

42. A combination for treating type 1 diabetes, Duchenne muscular dystrophy, liver disease or acute kidney disease in a subject, comprising: a) a first vector comprising a nucleic acid encoding Cas9 or dCas9; b) a second vector comprising a nucleic acid according to any one of claims 1 to 30 and a nucleic acid encoding an MS2 transcriptional activator fusion protein; A combination comprising:

43. (i) administering the composition increases expression of at least one gene target; or (ii) the subject is a human; 43. The combination of claim 42.

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