Engineered cas9 systems for eukaryotic genome modification

Abstract

To provide engineered Cas9 systems.SOLUTION: A system comprises an engineered Cas9 protein and an engineered guide RNA. The engineered guide RNA is designed to complex with the engineered Cas9 protein. The engineered guide RNA comprises a 5' guide sequence designed to hybridize with a target sequence in a double-stranded sequence, where the target sequence is 5' to a protospacer adjacent motif and has a specific sequence.SELECTED DRAWING: Figure 1

Description

[Technical field]

[0001] CROSS-REFERENCE TO RELATED APPLICATIONS This application claims the benefit of U.S. Provisional Application No. 62 / 631,304, filed February 15, 2018, and U.S. Provisional Application No. 62 / 720,525, filed August 21, 2018, each of which is incorporated herein by reference in its entirety.

[0002] Sequence Listing This application contains a Sequence Listing that has been submitted electronically in ASCII format, and is hereby incorporated by reference in its entirety. The ASCII copy, created on February 12, 2019, is named P18_023PCT_SL.txt and is 370,305 bytes in size.

[0003] Field The present disclosure relates to engineered Cas9 systems, nucleic acids encoding the systems, and methods of using the systems for genome modification. [Background technology]

[0004] background The recent development of bacterial class 2 clustered repeated short palindromic repeats (CRISPR) and CRISPR-associated (Cas) CRISPR / Cas systems as genome editing tools has provided unprecedented ease and simplicity of engineering site-specific endonucleases for eukaryotic genome modification. However, each CRISPR / Cas system requires a specific protospacer adjacent motif (PAM) for target DNA binding, so each system is limited to certain genomic sites. The currently most widely adopted Streptococcus pyogenes Cas9 (SpyCas9) uses a frequently occurring PAM (5'-NGG-3') for targeting, but is still excluded from many genomic sites that lack such motifs because eukaryotic genomes, especially mammalian genomes and plants, are highly complex and heterogeneous in DNA sequences. Furthermore, precise gene editing using homology-directed repair (HDR) or base editors such as dCas9 / cytidine deaminase and dCas9 / adenosine deaminase often requires precise DNA binding position, even at single base pair resolution, to achieve optimal editing results.Therefore, there is a need to develop novel CRISPR / Cas systems that use novel PAMs for targeting to increase genome coverage density. Summary of the Invention

[0005] overview Among the various aspects of the disclosure are engineered Cas9 systems comprising an engineered Cas9 protein and engineered guide RNAs, each engineered guide RNA designed to form a complex with an engineered Cas9 protein, the engineered guide RNAs comprising a 5' guide sequence designed to hybridize to a target sequence in a double stranded sequence, the target sequence being 5' to a protospacer adjacent motif (PAM), the PAM having a sequence listed in Table A.

[0006] Another aspect of the disclosure includes a plurality of nucleic acids encoding the engineered Cas9 system and at least one vector comprising a plurality of said nucleic acids.

[0007] Further aspects include eukaryotic cells comprising at least one engineered Cas9 system and / or at least one nucleic acid encoding said engineered Cas9 system.

[0008] Yet another aspect of the present disclosure includes a method for modifying a chromosomal sequence in a eukaryotic cell.The method includes introducing into a eukaryotic cell at least one engineered Cas9 system, including an engineered Cas9 protein and an engineered guide RNA, and / or at least one nucleic acid encoding the engineered Cas9 system, and optionally at least one donor polynucleotide, wherein the at least one engineered guide RNA guides the at least one engineered Cas9 protein to a target site in the chromosomal sequence, such that modification of the chromosomal sequence occurs.

[0009] Other aspects and features of the present disclosure are described in detail below. [Brief description of the drawings]

[0010] [Figure 1] Figure 1 shows a WebLogo analysis of the protospacer adjacent motif (PAM) required for in vitro targeted DNA cleavage by Cas9 orthologs. The numbers on the horizontal axis indicate the nucleotide position in the PAM sequence.

[0011] [Figure 2-1]FIG. 2A shows the cleavage efficiency (as a percentage of indels) of McaCas9, McaCas9-HN1HB1 fusion (i.e., HMGN1 at the amino terminus and HMGB1 box A at the carboxyl terminus), and McaCas9-HN1H1G fusion (i.e., HMGN1 at the amino terminus and histone H1 central globular motif at the carboxyl terminus). The target sites for each locus are shown in Table 6. Error bars indicate the mean ± SD (n=3 biological replicates). FIG. 2B shows the cleavage efficiency (as a percentage of indels) of PexCas9, PexCas9-HN1HB1 fusion (i.e., HMGN1 at the amino terminus and HMGB1 box A at the carboxyl terminus), and PexCas9-HN1H1G fusion (i.e., HMGN1 at the amino terminus and histone H1 central globular motif at the carboxyl terminus). The target sites for each locus are shown in Table 6. Error bars indicate the mean ± SD (n = 3 biological replicates).

[0012] [Figure 2-2] FIG. 2C shows the cleavage efficiency (as a percentage of indels) of BsmCas9, BsmCas9-HN1HB1 fusion (i.e., HMGN1 at the amino terminus and HMGB1 box A at the carboxyl terminus), and BsmCas9-HN1H1G fusion (i.e., HMGN1 at the amino terminus and histone H1 central globular motif at the carboxyl terminus). The target sites of each locus are shown in Table 6. Error bars show the mean ± SD (n=3 biological replicates). FIG. 2D shows the cleavage efficiency (as a percentage of indels) of LrhCas9, LrhCas9-HN1HB1 fusion (i.e., HMGN1 at the amino terminus and HMGB1 box A at the carboxyl terminus), and LrhCas9-HN1H1G fusion (i.e., HMGN1 at the amino terminus and histone H1 central globular motif at the carboxyl terminus). The target sites of each locus are shown in Table 6. Error bars indicate the mean ± SD (n = 3 biological replicates).

[0013] [Diagram 3]Figure 3 shows the off-target activity (as percent of indels) of control Cas9 and Cas9-CMM fusion nucleases. Error bars represent the mean ± SD (n=3 biological replicates). DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0014] Detailed Description The present disclosure provides orthologous Cas9 systems that use alternative PAMs for target DNA binding, thereby increasing genome coverage density. For example, some of these alternative PAMs contain A and / or T residues, while other alternative PAMS are GC-rich. Thus, engineered Cas9 systems that utilize these alternative PAMs enable targeted genome editing or genome modification of previously inaccessible genomic loci.

[0015] (I) Engineered Cas9 system One aspect of the disclosure provides an engineered Cas9 system comprising an engineered Cas9 protein and an engineered guide RNA, each engineered guide RNA designed to form a complex with a particular engineered Cas9 protein. Each engineered guide RNA comprises a 5' guide sequence designed to hybridize with a target sequence in a double-stranded sequence, the target sequence being 5' to a protospacer adjacent motif (PAM), the PAM having a sequence listed in Table A. These engineered Cas9 systems do not occur in nature.

[0016] (a) Engineered Cas9 protein The engineered Cas9 protein contains at least one amino acid substitution, insertion, or deletion compared to its wild-type counterpart. The Cas9 protein is a single effector protein in the type II CRISPR system present in various bacteria. The engineered Cas9 protein described herein is found in Acaryochloris spp., Acetohalobium spp., Acidaminococcus spp., Acidithiobacillus spp., Acidothermus spp., Akkermansia spp., Alicyclobacillus spp., Arrochromatium spp., and Streptococcus spp. Allochromatium spp., Ammonifex spp., Anabaena spp., Arthrospira spp., Bacillus spp., Bifidobacterium spp., Burkholderiales spp., Caldicelulosiruptor spp., Campylobacter spp., Candida spp. tus spp., Clostridium spp., Corynebacterium spp., Crocosphaera spp., Cyanothece spp., Exiguobacterium spp., Finegoldia spp., Francisella spp., Ktedonobacter spp., Lachnospiraceae spp. , Lactobacillus spp., Lyngbya spp., Marinobacter spp., Methanohalobium spp., Microscilla spp., Microcoleus spp., Microcystis spp., Mycoplasma spp., Natranaerobius spp., Neisseria spp.,Nitratifractor spp., Nitrosococcus spp., Nocardiopsis spp., Nodularia spp., Nostoc spp., Oenococcus spp., Oscillatoria spp., Parasutterella spp., Pelotomaculum spp., Petrotoga spp., Polaromonas spp., Prevotella spp. , Pseudoalteromonas spp., Ralstonia spp., Staphylococcus spp., Streptococcus spp., Streptomyces spp., Streptosporangium spp., Synechococcus spp., Thermosipho spp., Verrucomicrobia spp., and Wolinella spp.

[0017] In one embodiment, the engineered Cas9 proteins described herein are derived from Acidothermus spp., Akkermansia spp., Alicyclobacillus spp., Bacillus spp., Bifidobacterium spp., Burkholderia spp., Corynebacterium spp., Lactobacillus spp., Mycoplasma spp., Nitratifractor spp., Oenococcus spp., Parasatellella spp., Ralstonia spp., or Wolinella spp.

[0018] In certain embodiments, the engineered Cas9 proteins described herein are capable of inhibiting or inhibiting the expression of bacteria such as Acidothermus cellulolyticus (Ace), Akkermansia glycaniphila (Agl), Akkermansia muciniphila (Amu), Alicyclobacillus hesperidum (Ahe), Bacillus smithii (Bsm), Bifidobacterium bombi (Bbo), Corynebacterium diphtheria (Cdi), Lactobacillus rhamnosus (Lrh), Mycoplasma canis (Mycoplasma canis (Mca), Mycoplasma gallisepticum (Mga), Nitratifractor salsuginis (Nsa), Oenococcus kitaharae (Oki), Parasutterella excrementihominis (Pex), Ralstonia syzygii (Rsy), or Wolinella succinogenes (Wsu).

[0019] The wild-type Cas9 protein contains two nuclease domains, RuvC and HNH, each of which cleaves one strand of a double-stranded sequence. The Cas9 protein also contains a REC domain that interacts with a guide RNA (e.g., REC1, REC2) or an RNA / DNA heteroduplex (e.g., REC3), and a domain that interacts with a protospacer adjacent motif (PAM) (i.e., a PAM-interacting domain).

[0020] The Cas9 protein may be engineered to contain one or more modifications (i.e., at least one amino acid substitution, at least one amino acid deletion, at least one amino acid insertion) such that the Cas9 protein has altered activity, specificity, and / or stability.

[0021] For example, Cas9 protein may be engineered by one or more mutations and / or deletions to inactivate one or both of the nuclease domains. Inactivation of one nuclease domain produces a Cas9 protein that cleaves one strand of a double-stranded sequence (i.e., Cas9 nickase). The RuvC domain may be inactivated by mutations such as D10A, D8A, E762A, and / or D986A, and the HNH domain may be inactivated by mutations such as H840A, H559A, N854A, N856A, and / or N863A (based on the numbering system of Streptococcus pyogenes Cas9, SpyCas9). Inactivation of both nuclease domains produces a Cas9 protein that does not have cleavage activity (i.e., catalytically inactive or dead Cas9).

[0022] The Cas9 protein may also be engineered with one or more amino acid substitutions, deletions, and / or insertions to have improved targeting specificity, improved fidelity, altered PAM specificity, reduced off-target effects, and / or increased stability. Non-limiting examples of one or more mutations that improve targeting specificity, improve fidelity, and / or reduce off-target effects include N497A, R661A, Q695A, K810A, K848A, K855A, Q926A, K1003A, R1060A, and / or D1135E (based on the SpyCas9 numbering system).

[0023] (i) Foreign Domains Cas9 protein may be engineered to contain at least one heterologous domain, i.e., Cas9 is fused to one or more heterologous domains. In the situation where two or more heterologous domains are fused to Cas9, the two or more heterologous domains may be the same or they may be different. One or more heterologous domains may be fused to the N-terminus, C-terminus, internal position, or a combination thereof. Fusion may be direct via chemical bond, or binding may be indirect via one or more linkers. In various embodiments, the heterologous domain may be a nuclear localization signal, a cell membrane permeation domain, a marker domain, a chromatin disruption domain, an epigenetic modification domain (e.g., a cytidine deaminase domain, a histone acetyltransferase domain, etc.), a transcriptional control domain, an RNA aptamer binding domain, or a non-Cas9 nuclease domain.

[0024] In some embodiments, one or more heterologous domains may be a nuclear localization signal (NLS). Non-limiting examples of nuclear localization signals include PKKKRKV (SEQ ID NO: 78), PKKKRRV (SEQ ID NO: 79), KRPAATKKAGQAKKKK (SEQ ID NO: 80), YGRKKRRQRRR (SEQ ID NO: 81), RKKRRQRRR (SEQ ID NO: 82), PAAKRVKLD (SEQ ID NO: 83), RQRRNELKRSP (SEQ ID NO: 84), VSRKRPRP (SEQ ID NO: 85), PPKKARED (SEQ ID NO: 86), PQPKKKPL (SEQ ID NO: 87), SALIKKKKMAP (SEQ ID NO: 88), and PKKKRRV (SEQ ID NO: 89). No.:88), PKQKKRK (SEQ ID NO:89), RKLKKKIKKL (SEQ ID NO:90), REKKKFLKRR (SEQ ID NO:91), KRKGDEVDGVDEVAKKKSKK (SEQ ID NO:92), RKCLQAGMNLEARKTKK (SEQ ID NO:93), NQSSNFGPMKGGNFGGRSSGPYGGGGQYFAKPRNQGGY (SEQ ID NO:94), and RMRIZFKNKGKDTAELRRRRVEVSVELRKAKKDEQILKRRNV (SEQ ID NO:95).

[0025] In other embodiments, the one or more heterologous domains can be a cell membrane penetrating domain. Examples of suitable cell membrane permeation domains include, but are not limited to, GRKKRRQRRRPPQPKKKRKV (SEQ ID NO: 96), PLSSIFSRIGDPPKKKRKV (SEQ ID NO: 97), GALFLGWLGAAGSTMGAPKKKRKV (SEQ ID NO: 98), GALFLGFLGAAGSTMGAWSQPKKKRKV (SEQ ID NO: 99), KETWWETWWTEWSQPKKKRKV (SEQ ID NO: 100), YARAAARQARA (SEQ ID NO: 101), THRLPRRRRRR (SEQ ID NO: 102), GGRRARRRRRR (SEQ ID NO: 103), RRQRRTSKLMKR (SEQ ID NO: 104), GWTLNSAGYLLGKINLKALAALAKKIL (SEQ ID NO: 105), KALAWEAKLAKALAKALAKHLAKALAKALKCEA (SEQ ID NO: 106), and RQIKIWFQNRRMKWKK (SEQ ID NO: 107).

[0026] In alternative embodiments, one or more heterologous domains may be a marker domain. Marker domains include fluorescent proteins and purification or epitope tags. Suitable fluorescent proteins include, but are not limited to, green fluorescent proteins (e.g., GFP, eGFP, GFP-2, tagGFP, turboGFP, Emerald, Azami Green, Monomeric Azami Green, CopGFP, AceGFP, ZsGreen1), yellow fluorescent proteins (e.g., YFP, EYFP, Citrine, Venus, YPet, PhiYFP, ZsYellow1), blue fluorescent proteins (e.g., BFP, EBFP, EBFP2, Azurite, mKalama1, GFPuv, Sapphire, T-sapphire), cyan fluorescent proteins (e.g., ECFP, Cerulean, CyPet, AmCyan1, Midoriishi-Cyan), red fluorescent proteins (e.g., mKate, mKate2, mPlum, DsRed, etc.). Monomer, mCherry, mRFP1, DsRed-Express, DsRed2, DsRed-Monomer, HcRed-Tandem, HcRed1, AsRed2, eqFP611, mRasberry, mStrawberry, Jred), orange fluorescent protein (e.g., mOrange, mKO, Kusabira-Orange, Monomeric Kusabira-Orange, mTangerine, tdTomato), or combinations thereof. The marker domain may comprise tandem repeats of one or more fluorescent proteins (e.g., Suntag). Non-limiting examples of suitable purification or epitope tags include 6xHis (SEQ ID NO: 134), FLAG®, HA, GST, Myc, SAM, and the like.Non-limiting examples of heterologous fusions that facilitate detection or enrichment of CRISPR complexes include streptavidin (Kipriyanov et al., Human Antibodies, 1995, 6(3):93-101.), avidin (Airenne et al., Biomolecular Engineering, 1999, 16(1-4):87-92), monomeric forms of avidin (in (Laitinen et al., Journal of Biological Chemistry, 2003, 278(6):4010-4014), and peptide tags that facilitate biotinylation during recombinant production (Cull et al., Methods in Enzymology, 2000, 326:430-440).

[0027] In yet other embodiments, the one or more heterologous domains may be chromatin regulatory motifs (CMMs). Non-limiting examples of CMMs include high mobility group (HMG) proteins (e.g., HMGB1, HMGB2, HMGB3, HMGN1, HMGN2, HMGN3a, HMGN3b, HMGN4, and HMGN5 proteins), the central globular domains of histone H1 variants (e.g., histones H1.0, H1.1, H1.2, H1.3, H1.4, H1.5, H1.6, H1.7, H1.8, H1.9, and H.1.10), or DNA binding domains of chromatin remodeling complexes (e.g., SWI / SNF (Switch / Sucrose Nonfermenting ( SWI tch / S ucrose N on- F ermentable), ISWI (imitation switch ( I Mitigation SWI tch), CHD (chromodomain-helicase-DNA binding ( C hromodomain- H Elicase- DNA binding), Mi-2 / NuRD (nucleosome remodeling and deacetylase), INO80, SWR1, and nucleosome interacting peptides derived from the RSC complex. In other embodiments, the CMMs may also be derived from topoisomerases, helicases, or viral proteins. The source of the CMMs may and will vary. The CMMs may be human, animal (i.e., vertebrate and invertebrate), plant, algae, or yeast. Non-limiting examples of specific CMMs are listed in the table below. Those skilled in the art can readily identify homologs in other species and / or associated fusion motifs therewith. [Table a]

[0028] In yet other embodiments, one or more heterologous domains may be epigenetic modification domains. Non-limiting examples of suitable epigenetic modification domains include DNA deamination (e.g., cytidine deaminase, adenosine deaminase, guanine deaminase), DNA methyltransferase activity (e.g., cytosine methyltransferase), DNA demethylase activity, DNA amination, DNA oxidation activity, DNA helicase activity, histone acetyltransferase (HAT) activity (e.g., the HAT domain from the E1A binding protein p300), histone deacetylase activity, histone methyltransfer ... In certain embodiments, the epigenetic modification domain may comprise cytidine deaminase activity, adenosine deaminase activity, histone acetyltransferase activity, histone demethylase activity, histone kinase activity, histone phosphatase activity, histone ubiquitin ligase activity, histone deubiquitination activity, histone adenylation activity, histone deadenylation activity, histone sumoylation activity, histone desumoylation activity, histone ribosylation activity, histone deribosylation activity, histone myristoylation activity, histone demyristoylation activity, histone citrullination activity, histone alkylation activity, histone dealkylation activity, or histone oxidation activity. In certain embodiments, the epigenetic modification domain may comprise cytidine deaminase activity, adenosine deaminase activity, histone acetyltransferase activity, or DNA methyltransferase activity.

[0029] In other embodiments, the one or more heterologous domains may be transcriptional regulatory domains (i.e., transcriptional activation domains or transcriptional repressor domains). Suitable transcriptional activation domains include, without limitation, herpes simplex virus VP16 domain, VP64 (i.e., four tandem copies of VP16), VP160 (i.e., ten tandem copies of VP16), NFκB p65 activation domain (p65), Epstein-Barr virus R transcriptional activator (Rta) domain, VPR (i.e., VP64+p65+Rta), p300-dependent transcriptional activation domain, p53 activation domains 1 and 2, heat shock factor 1 (HSF1) activation domain, Smad4 activation domain (SAD), cAMP response element binding protein (CREB) activation domain, E2A activation domain, nuclear factor of activated T cells (NFAT) activation domain, or combinations thereof. Non-limiting examples of suitable transcriptional repressor domains include Kruppel-associated box (KRAB) repressor domain, Mxi repressor domain, inducible cAMP early repressor (ICER) domain, YY1 glycine-rich repressor domain, Sp1-like repressor, E(spl) repressor, IκB repressor, Sin3 repressor, methyl-CpG binding protein 2 (MeCP2) repressor, or combinations thereof. The transcriptional activation or repressor domain may be genetically fused to the Cas9 protein or may be attached via non-covalent protein-protein, protein-RNA, or protein-DNA interactions.

[0030] In further embodiments, one or more heterologous domains may be an RNA aptamer binding domain (Konermann et al., Nature, 2015, 517(7536):583-588; Zalatan et al., Cell, 2015, 160(1-2):339-50). Examples of suitable RNA aptamer protein domains include MS2 coat protein (MCP), PP7 bacteriophage coat protein (PCP), Mu bacteriophage Com protein, lambda bacteriophage N22 protein, stem-loop binding protein (SLBP), fragile X mental retardation syndrome-associated protein 1 (FXR1), proteins derived from bacteriophages such as AP205, BZ13, f1, f2, fd, fr, ID2, JP34 / GA, JP501, JP34, JP500, KU1, M11, M12, MX1, NL95, PP7, ΦCb5, ΦCb8r, ΦCb12r, ΦCb23r, Qβ, R17, SP-β, TW18, TW19, and VK, fragments thereof, or derivatives thereof.

[0031] In yet other embodiments, one or more heterologous domains may be non-Cas9 nuclease domains. Suitable nuclease domains can be obtained from any endonuclease or exonuclease. Non-limiting examples of endonucleases from which nuclease domains can be derived include, but are not limited to, restriction endonucleases and homing endonucleases. In some embodiments, nuclease domains may be derived from type II-S restriction endonucleases. Type II-S endonucleases typically cleave DNA at a site several base pairs away from the recognition / binding site and have separable binding and cleavage domains. These enzymes are generally monomers that temporarily associate, form dimers, and cleave each strand of DNA at alternate positions. Non-limiting examples of suitable type II-S endonucleases include BfiI, BpmI, BsaI, BsgI, BsmBI, BsmI, BspMI, FokI, MboII, and SapI. In some embodiments, the nuclease domain may be a FokI nuclease domain or a derivative thereof. The type II-S nuclease domain may be modified to facilitate the dimerization of two different nuclease domains. For example, the cleavage domain of FokI may be modified by mutating specific amino acid residues. As a non-limiting example, the amino acid residues at positions 446, 447, 479, 483, 484, 486, 487, 490, 491, 496, 498, 499, 500, 531, 534, 537, and 538 of the FokI nuclease domain are targets for modification. In certain embodiments, the FokI nuclease domain may comprise a first FokI half-domain that comprises a Q486E, I499L, and / or N496D mutation, and a second FokI half-domain that comprises an E490K, I538K, and / or H537R mutation.

[0032] The one or more heterologous domains may be directly linked to the Cas9 protein via one or more chemical bonds (e.g., covalent bonds) or the one or more heterologous domains may be indirectly linked to the Cas9 protein via one or more linkers.

[0033] A linker is a chemical group that links to one or more other chemical groups via at least one covalent bond. Suitable linkers include amino acids, peptides, nucleotides, nucleic acids, organic linker molecules (e.g., maleimide derivatives, N-ethoxybenzylimidazole, biphenyl-3,4',5-tricarboxylic acid, p-aminobenzyloxycarbonyl, etc.), disulfide linkers, and polymer linkers (e.g., PEG). A linker may include one or more spacing groups, including, but not limited to, alkylene, alkenylene, alkynylene, alkyl, alkenyl, alkynyl, alkoxy, aryl, heteroaryl, aralkyl, aralkenyl, aralkynyl, etc. A linker may be neutral or may have a positive or negative charge. Additionally, a linker may be cleavable such that the covalent bond of the linker that connects the linker to another chemical group can be broken or cleaved under certain conditions, including pH, temperature, salt concentration, light, catalyst, or enzyme. In some embodiments, the linker may be a peptide linker. The peptide linker may be a flexible amino acid linker (e.g., containing small non-polar or polar amino acids). Non-limiting examples of flexible linkers include LEGGGS (SEQ ID NO: 108), TGSG (SEQ ID NO: 109), GGSGGGSG (SEQ ID NO: 110), (GGGGS) 1-4 (SEQ ID NO: 111), and (Gly) 6-8 (SEQ ID NO: 112). Alternatively, the peptide linker may be a rigid amino acid linker. Such a linker includes (EAAAK) 1-4 (SEQ ID NO: 113), A(EAAAK) 2-5 A (SEQ ID NO: 114), PAPAP (SEQ ID NO: 115), and (AP) 6-8 (SEQ ID NO:116). Further examples of suitable linkers are well known in the art, and programs for designing linkers are readily available (Crasto et al., Protein Eng., 2000, 13(5):309-312).

[0034] In some embodiments, the engineered Cas9 protein may be produced recombinantly in a cell-free system, bacterial cells, or eukaryotic cells and purified using standard purification means, hi other embodiments, the engineered Cas9 protein is produced in vivo in a eukaryotic cell of interest from a nucleic acid encoding the engineered Cas9 protein (see section (II) below).

[0035] In an embodiment where the engineered Cas9 protein comprises nuclease or nickase activity, the engineered Cas9 protein may further comprise at least one nuclear localization signal, cell membrane permeation domain, and / or marker domain, and at least one chromatin disruption domain.In an embodiment where the engineered Cas9 protein is linked to an epigenetic modification domain, the engineered Cas9 protein may further comprise at least one nuclear localization signal, cell membrane permeation domain, and / or marker domain, and at least one chromatin disruption domain.Furthermore, in an embodiment where the engineered Cas9 protein is linked to a transcriptional control domain, the engineered Cas9 protein may further comprise at least one nuclear localization signal, cell membrane permeation domain, and / or marker domain, and at least one chromatin disruption domain and / or at least one RNA aptamer binding domain.

[0036] (ii) a specific engineered Cas9 protein In certain embodiments, the engineered Cas9 protein is derived from Bacillus smithii, Lactobacillus rhamnosus, Parasatellella exclementihominis, Mycoplasma canis, Mycoplasma gallisepticum, Akkermansia glycaniphila, Akkermansia muciniphila, Oenococcus Kitaharae, Bifidobacterium bombyi, Acidothermus cellulolyticus, Alicyclobacillus hesperidum, Wolinella succinogenes, Nitratiphracter sarusginis, Ralstonia szygii, or Corynebacterium diphtheriae and is linked to at least one NLS. In some iterations, the engineered Cas9 protein may have at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, or at least about 99% sequence identity to SEQ ID NO: 2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, or 30. In one embodiment, the engineered Cas9 protein may have at least about 95% sequence identity to SEQ ID NO: 2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, or 30. In other iterations, the engineered Cas9 protein has the amino acid sequence of SEQ ID NO: 2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, or 30.

[0037] In other embodiments, the engineered Cas9 protein may be a Cas9 protein of Bacillus smithii, Lactobacillus rhamnosus, Parasatellella exclementihominis, Mycoplasma canis, Mycoplasma gallisepticum, Akkermansia glycaniphila, Akkermansia muciniphila, Oenococcus kitaharae, Bifidobacterium bombyi, Acidothermus cellulolyticus, Alicyclobacillus hesperidum, Wallinella succinogenes, Nitratiphracter sarusginis, Ralstonia szygii, or Corynebacterium diphtheriae linked to at least one chromatin regulatory motif (CMM). The linkage between the Cas9 protein and the CMM may be direct or via a linker. The Cas9-CMM fusion protein may further comprise at least one NLS. In certain embodiments, the Cas9-CMM fusion protein may have at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, or at least about 99% sequence identity to SEQ ID NO: 117, 118, 119, 1200, 121, 122, 123, or 124. In one embodiment, the Cas9-CMM fusion protein may have at least about 95% sequence identity to SEQ ID NO: 117, 118, 119, 120, 121, 122, 123, or 124. In certain iterations, the Cas9-CMM fusion protein has the amino acid sequence of SEQ ID NO: 117, 118, 119, 120, 121, 122, 123, or 124.

[0038] (b) Engineered guide RNA The engineered guide RNA is designed to form a complex with a specific engineered Cas9 protein. The guide RNA comprises (i) a CRISPR RNA (crRNA) that contains a guide sequence at the 5' end that hybridizes with the target sequence, and (ii) a trans-acting crRNA (tracrRNA) sequence that recruits the Cas9 protein. The crRNA guide sequence of each guide RNA is different (i.e., sequence-specific). The tracrRNA sequence is generally the same in guide RNAs designed to form a complex with the Cas9 protein from a specific bacterial species.

[0039] The crRNA guide sequence is designed to hybridize with the target sequence (i.e., protospacer) in a double-stranded sequence. Generally, the complementarity between the crRNA and the target sequence is at least 80%, at least 85%, at least 90%, at least 95%, or at least 99%. In certain embodiments, the complementarity is complete (i.e., 100%). In various embodiments, the length of the crRNA guide sequence may range from about 15 nucleotides to about 25 nucleotides. For example, the crRNA guide sequence may be about 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, or 25 nucleotides long. In certain embodiments, the crRNA is about 19, 20, or 21 nucleotides long. In one embodiment, the crRNA guide sequence has a length of 20 nucleotides.

[0040] The guide RNA comprises a repeat sequence that forms at least one stem-loop structure that interacts with the Cas9 protein, and a 3' sequence that remains single-stranded. The length of each loop and stem may vary. For example, the loop may range from about 3 to about 10 nucleotides in length, and the stem may range from about 6 to about 20 base pairs in length. The stem may include one or more overhangs of 1 to about 10 nucleotides. The length of the single-stranded 3' region may vary. The tracrRNA sequence in the engineered guide RNA is generally based on the wild-type tracrRNA coding sequence in the bacterial species of interest. The wild-type sequence may be modified to facilitate the formation of secondary structures, to increase the stability of the secondary structures, to facilitate expression in eukaryotic cells, etc. For example, one or more nucleotide changes may be introduced into the guide RNA coding sequence (see Example 3 below). The tracrRNA sequence may range from about 50 nucleotides to about 300 nucleotides in length. In various embodiments, the tracrRNA may range in length from about 50 to about 90 nucleotides, about 90 to about 110 nucleotides, about 110 to about 130 nucleotides, about 130 to about 150 nucleotides, about 150 to about 170 nucleotides, about 170 to about 200 nucleotides, about 200 to about 250 nucleotides, or about 250 to about 300 nucleotides.

[0041] Generally, an engineered guide RNA is a single molecule (i.e., a single guide RNA or sgRNA) in which the crRNA sequence is linked to the tracrRNA sequence. In some embodiments, however, the engineered guide RNA may be two separate molecules. The first molecule comprises a crRNA that includes a 3' sequence (comprising about 6 to about 20 nucleotides) that can base pair with the 5' end of the second molecule, and the second molecule comprises a tracrRNA that includes a 5' sequence (comprising about 6 to about 20 nucleotides) that can base pair with the 3' end of the first molecule.

[0042] In some embodiments, the tracrRNA sequence of the engineered guide RNA may be modified to include one or more aptamer sequences (Konermann et al., Nature, 2015, 517(7536):583-588; Zalatan et al., Cell, 2015, 160(1-2):339-50). Suitable aptamer sequences include those that bind an adaptor protein selected from MCP, PCP, Com, SLBP, FXR1, AP205, BZ13, f1, f2, fd, fr, ID2, JP34 / GA, JP501, JP34, JP500, KU1, M11, M12, MX1, NL95, PP7, ΦCb5, ΦCb8r, ΦCb12r, ΦCb23r, Qβ, R17, SP-β, TW18, TW19, VK, fragments thereof, or derivatives thereof. One of skill in the art will appreciate that the length of the aptamer sequence may vary.

[0043] In other embodiments, the guide RNA may further comprise at least one detectable label. The detectable label may be a fluorophore (e.g., FAM, TMR, Cy3, Cy5, Texas Red, Oregon Green, Alexa Fluors, Halo tags, or suitable fluorescent dyes), a detection tag (e.g., biotin, digoxigenin, etc.), a quantum dot, or a gold particle.

[0044] The guide RNA may comprise standard ribonucleotides and / or modified ribonucleotides. In some embodiments, the guide RNA may comprise standard or modified deoxyribonucleotides. In embodiments where the guide RNA is enzymatically synthesized (i.e., in vivo or in vitro), the guide RNA generally comprises standard ribonucleotides. In embodiments where the guide RNA is chemically synthesized, the guide RNA may comprise standard or modified ribonucleotides and / or deoxyribonucleotides. The modified ribonucleotides and / or deoxyribonucleotides include base modifications (e.g., pseudouridine, 2-thiouridine, N6-methyladenosine, etc.) and / or sugar modifications (e.g., 2'-O-methyl, 2'-fluoro, 2'-amino, locked nucleic acid (LNA), etc.). The backbone of the guide RNA may also be modified to include phosphorothioate linkages, boranophosphate linkages, or peptide nucleic acids.

[0045] In certain embodiments, the engineered guide RNA has at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, or at least about 99% sequence identity to SEQ ID NO: 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, or 45. In some embodiments, the engineered Cas9 guide RNA has the sequence of SEQ ID NO: 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, or 45.

[0046] (c) PAM sequence The above detailed engineered Cas9 system targets a specific sequence in double-stranded DNA located upstream of a novel PAM sequence. The PAM sequence preferred by the engineered Cas9 system was identified in vitro using a library of degenerate PAMS (see Example 1 and Figure 1) and confirmed by sequencing after genome editing experiments (see Example 2). The PAM for each of the engineered Cas9 systems described herein is shown in Table A below. [Table A] *K is G or T; M is A or C; R is A or G; Y is C or T; N is A, C, G, or T.

[0047] (II) Nucleic acid A further aspect of the present disclosure provides a nucleic acid encoding the engineered Cas9 system described above in section (I). The system may be encoded by a single nucleic acid or multiple nucleic acids. The nucleic acid may be DNA or RNA, linear or circular, single-stranded or double-stranded. The RNA or DNA may be codon optimized for efficient translation into protein in the eukaryotic cell of interest. Codon optimization programs are available as freeware or from commercial sources.

[0048] In some embodiments, the nucleic acid encodes a protein having at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, or at least about 99% sequence identity to the amino acid sequence of SEQ ID NO: 2, 4, 6, 8, 10, 12, 14, 16, 18, 20, 22, 24, 26, 28, or 30. In one embodiment, the nucleic acid encoding the engineered Cas9 protein may have at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, or at least about 99% sequence identity to the DNA sequence of SEQ ID NO: 1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, or 29. In one embodiment, the DNA encoding the engineered Cas9 protein has the DNA sequence of SEQ ID NO: 1, 3, 5, 7, 9, 11, 13, 15, 17, 19, 21, 23, 25, 27, or 29. In further embodiments, the nucleic acid encodes a protein having at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, or at least about 99% sequence identity to the amino acid sequence of SEQ ID NO: 117, 118, 119, 120, 121, 122, 123, or 124.

[0049] In some embodiments, the nucleic acid encoding the engineered Cas9 protein may be RNA. The RNA may be enzymatically synthesized in vitro. Thus, the DNA encoding the engineered Cas9 protein may be operably linked to a promoter sequence recognized by a phage RNA polymerase for in vitro RNA synthesis. For example, the promoter sequence may be a T7, T3, or SP6 promoter sequence or a variant of a T7, T3, or SP6 promoter sequence. The DNA encoding the engineered protein may be part of a vector, as described in detail below. In such embodiments, the in vitro transcribed RNA may be purified, capped, and / or polyadenylated. In other embodiments, the RNA encoding the engineered Cas9 protein may be part of a self-replicating RNA (Yoshioka et al., Cell Stem Cell, 2013, 13:246-254). The self-replicating RNA may be derived from a non-infectious, self-replicating Venezuelan Equine Encephalitis (VEE) virus RNA replicon, which is a single-stranded positive-stranded RNA that allows self-replication for a limited number of cell divisions and can be modified to encode a protein of interest (Yoshioka et al., Cell Stem Cell, 2013, 13:246-254).

[0050] In other embodiments, the nucleic acid encoding the engineered Cas9 protein may be DNA. The DNA coding sequence may be operably linked to at least one promoter control sequence for expression in a cell of interest. In one embodiment, the DNA coding sequence may be operably linked to a promoter sequence for expression of the engineered Cas9 protein in a bacterial (e.g., E. coli) cell or a eukaryotic (e.g., yeast, insect, or mammalian) cell. Suitable bacterial promoters include, without limitation, T7 promoter, lac operon promoter, trp promoter, tac promoter (which is a hybrid of the trp and lac promoters), mutations of any of the foregoing, and combinations of any of the foregoing. Non-limiting examples of suitable eukaryotic promoters include constitutive, regulated, or cell or tissue specific promoters. Suitable eukaryotic constitutive promoter control sequences include, but are not limited to, the cytomegalovirus immediate early promoter (CMV), the simian virus (SV40) promoter, the adenovirus major late promoter, the Rous sarcoma virus (RSV) promoter, the mouse mammary tumor virus (MMTV) promoter, the phosphoglycerate kinase (PGK) promoter, the elongation factor (ED1)-alpha promoter, the ubiquitin promoter, the actin promoter, the tubulin promoter, the immunoglobulin promoter, fragments thereof, or combinations of any of the foregoing. Examples of suitable eukaryotic regulated promoter control sequences include, but are not limited to, those regulated by heat shock, metals, steroids, antibiotics, or alcohol. Non-limiting examples of tissue-specific promoters include B29 promoter, CD14 promoter, CD43 promoter, CD45 promoter, CD68 promoter, desmin promoter, elastase-1 promoter, endoglin promoter, fibronectin promoter, Flt-1 promoter, GFAP promoter, GPIIb promoter, ICAM-2 promoter, INF-β promoter, Mb promoter, NphsI promoter, OG-2 promoter, SP-B promoter, SYN1 promoter, and WASP promoter.The promoter sequence may be wild-type, or it may be modified for more efficient or effective expression. In some embodiments, the DNA coding sequence may also be linked to a polyadenylation signal (e.g., SV40 polyA signal, bovine growth hormone (BGH) polyA signal, etc.) and / or at least one transcription termination sequence. In some situations, the engineered Cas9 protein may be purified from bacteria or eukaryotic cells.

[0051] In yet other embodiments, the engineered guide RNA may be encoded by DNA. In some cases, the DNA encoding the engineered guide RNA may be operably linked to a promoter sequence recognized by a phage RNA polymerase for in vitro RNA synthesis. For example, the promoter sequence may be a T7, T3, or SP6 promoter sequence or a variant of a T7, T3, or SP6 promoter sequence. In other examples, the DNA encoding the engineered guide RNA may be operably linked to a promoter sequence recognized by an RNA polymerase III (Pol III) for expression in a eukaryotic cell of interest. Examples of suitable Pol III promoters include, but are not limited to, mammalian U6, U3, H1, and 7SL RNA promoters.

[0052] In various embodiments, the nucleic acid encoding the engineered Cas9 protein may be present in a vector. In some embodiments, the vector may further comprise a nucleic acid encoding an engineered guide RNA. Suitable vectors include plasmid vectors, viral vectors, and self-replicating RNA (Yoshioka et al., Cell Stem Cell, 2013, 13:246-254). In some embodiments, the nucleic acid encoding the composite or fusion protein may be present in a plasmid vector. Non-limiting examples of suitable plasmid vectors include pUC, pBR322, pET, pBluescript, and variants thereof. In other embodiments, the nucleic acid encoding the composite or fusion protein may be part of a viral vector (e.g., a lentiviral vector, an adeno-associated viral vector, an adenoviral vector, etc.). The plasmid or viral vector may comprise additional expression control sequences (e.g., enhancer sequences, Kozak sequences, polyadenylation sequences, transcription termination sequences, etc.), selectable marker sequences (e.g., antibiotic resistance genes), origins of replication, etc. Further information about vectors and their use can be found in "Current Protocols in Molecular Biology" Ausubel et al., John Wiley & Sons, New York, 2003 or "Molecular Cloning: A Laboratory Manual" Sambrook & Russell, Cold Spring Harbor Press, Cold Spring Harbor, NY, 3rd edition, 2001.

[0053] (III) Eukaryotic cells Another aspect of the present disclosure includes a eukaryotic cell comprising at least one engineered Cas9 system as described in detail in section (I) and / or at least one nucleic acid encoding an engineered Cas9 protein and / or an engineered guide RNA as described in detail in section (II).

[0054] The eukaryotic cell may be a human cell, a non-human mammalian cell, a non-mammalian vertebrate cell, an invertebrate cell, a plant cell, or a unicellular eukaryote. Examples of suitable eukaryotic cells are described in detail in section (IV)(c). The eukaryotic cell may be in vitro, ex vivo, or in vivo.

[0055] (IV) Methods for modifying chromosomal sequences Further aspects of the disclosure include methods for modifying chromosomal sequences in eukaryotic cells. Generally, the methods include introducing into a eukaryotic cell of interest at least one engineered Cas9 system, as described in detail in section (I), and / or at least one nucleic acid encoding the engineered Cas9 protein, as described in detail in section (II).

[0056] In embodiments in which the engineered Cas9 protein comprises nuclease or nickase activity, the chromosomal sequence modification may comprise a substitution of at least one nucleotide, a deletion of at least one nucleotide, or an insertion of at least one nucleotide. In some iterations, the method comprises introducing into a eukaryotic cell one engineered Cas9 system comprising nuclease activity or two engineered Cas9 systems comprising nickase activity and no donor polynucleotide, such that the engineered Cas9 system or systems introduce a double-stranded break at a target site in the chromosomal sequence, and repair of the double-stranded break by cellular DNA repair processes introduces at least one nucleotide change (i.e., an indel), thereby inactivating the chromosomal sequence (i.e., a gene knockout). In other iterations, the method involves introducing into a eukaryotic cell one engineered Cas9 system that contains nickase activity, or two engineered Cas9 systems that contain nickase activity as well as a donor polynucleotide, such that the engineered Cas9 system or systems introduce a double-stranded break at a target site in the chromosomal sequence, and repair of the double-stranded break by cellular DNA repair processes results in the insertion or replacement of a sequence in the donor polynucleotide at the target site in the chromosomal sequence (i.e., gene correction or gene knock-in).

[0057] In embodiments in which the engineered Cas9 protein comprises epigenetic modifying activity or transcriptional regulatory activity, the chromosomal sequence modification may comprise alteration of at least one nucleotide at or near the target site, modification of at least one nucleotide at or near the target site, modification of at least one histone protein at or near the target site, and / or alteration of transcription at or near the target site in the chromosomal sequence.

[0058] (a) Introduction into cells As described above, the methods include introducing into a eukaryotic cell at least one engineered Cas9 system and / or a nucleic acid encoding said system (and a donor polynucleotide, if desired). The at least one system and / or nucleic acid / donor polynucleotide may be introduced into the cell of interest by a variety of means.

[0059] In some embodiments, cells may be transfected with appropriate molecules (i.e., proteins, DNA, and / or RNA). Suitable transfection methods include nucleofection (or electroporation), calcium phosphate-mediated transfection, cationic polymer transfection (e.g., DEAE-dextran or polyethyleneimine), viral transduction, virosome transfection, virion transfection, liposome transfection, cationic liposome transfection, immunoliposome transfection, non-liposomal lipid transfection, dendrimer transfection, heat shock transfection, magnetofection, lipofection, gene gun delivery, impalefection, sonoporation, optical transfection, and proprietary agent-enhanced uptake of nucleic acids. Transfection methods are well known in the art (see, for example, "Current Protocols in Molecular Biology" Ausubel et al., John Wiley & Sons, New York, 2003 or "Molecular Cloning: A Laboratory Manual" Sambrook & Russell, Cold Spring Harbor Press, Cold Spring Harbor, NY, 3rd edition, 2001). In other embodiments, molecules may be introduced into cells by microinjection. For example, molecules may be injected into the cytoplasm or nucleus of a cell of interest. The amount of each molecule introduced into a cell may vary, but those skilled in the art are familiar with the means to determine the appropriate amount.

[0060] The various molecules may be introduced into the cell simultaneously or sequentially. For example, the engineered Cas9 system (or its encoding nucleic acid) and the donor polynucleotide may be introduced simultaneously. Alternatively, one may be introduced into the cell first, and then the other may be introduced later.

[0061] Generally, cells are maintained under suitable conditions for cell growth and / or maintenance. Suitable cell culture conditions are well known in the art and described, for example, in Santiago et al., Proc. Natl. Acad. Sci. USA, 2008, 105:5809-5814; Moehle et al. Proc. Natl. Acad. Sci. USA, 2007, 104:3055-3060; Urnov et al., Nature, 2005, 435:646-651; and Lombardo et al., Nat. Biotechnol., 2007, 25:1298-1306. Those skilled in the art understand that methods for culturing cells are known in the art and can and will vary depending on cell type. In all cases, routine optimization can be used to determine the optimal technique for a particular cell type.

[0062] (b) a desired donor polynucleotide In embodiments in which the engineered Cas9 protein comprises nuclease or nickase activity, the method may further comprise introducing at least one donor polynucleotide into the cell. The donor polynucleotide may be single-stranded or double-stranded, linear or circular, and / or RNA or DNA. In some embodiments, the donor polynucleotide may be a vector, e.g., a plasmid vector.

[0063] The donor polynucleotide comprises at least one donor sequence. In some aspects, the donor sequence of the donor polynucleotide may be a modified version of an endogenous or natural chromosomal sequence. For example, the donor sequence may be essentially identical to a portion of the chromosomal sequence at or near the sequence targeted by the engineered Cas9 system, but contains at least one nucleotide change. Thus, upon integration or replacement with the natural sequence, the sequence at the targeted chromosomal position contains at least one nucleotide change. For example, the change may be an insertion of one or more nucleotides, a deletion of one or more nucleotides, a substitution of one or more nucleotides, or a combination thereof. As a result of the "genetic correction" integration of the modified sequence, the cell can produce a modified gene product from the targeted chromosomal sequence.

[0064] In other aspects, the donor sequence of the donor polynucleotide may be an exogenous sequence. As used herein, an "exogenous" sequence refers to a sequence that is not native to the cell or whose natural location is a different location in the genome of the cell. For example, the exogenous sequence may include a protein coding sequence that may be operably linked to an exogenous promoter control sequence such that upon integration into the genome, the cell can express the protein encoded by the integrated sequence. Alternatively, the exogenous sequence may be integrated into a chromosomal sequence such that its expression is regulated by an endogenous promoter control sequence. In other iterations, the exogenous sequence may be a transcription control sequence, another expression control sequence, an RNA coding sequence, etc. As mentioned above, the integration of an exogenous sequence into a chromosomal sequence is referred to as "knock-in".

[0065] As can be understood by one of skill in the art, the length of the donor sequence can and will vary, for example, the donor sequence can vary in length from a few nucleotides to a few hundred nucleotides to a few hundred thousand nucleotides.

[0066] Typically, the donor sequence in the donor polynucleotide is flanked by upstream and downstream sequences that have substantial sequence identity to sequences located upstream and downstream, respectively, of the sequence targeted by the engineered Cas9 system. Due to these sequence similarities, the upstream and downstream sequences of the donor polynucleotide allow for homologous recombination between the donor polynucleotide and the targeted chromosomal sequence, such that the donor sequence may be integrated into (or exchanged with) the chromosomal sequence.

[0067] As used herein, upstream sequence refers to a nucleic acid sequence that shares substantial sequence identity with the upstream chromosomal sequence of the sequence targeted by engineered Cas9 system.Similarly, downstream sequence refers to a nucleic acid sequence that shares substantial sequence identity with the downstream chromosomal sequence of the sequence targeted by engineered Cas9 system.As used herein, the phrase "substantial sequence identity" refers to a sequence that has at least about 75% sequence identity.Thus, the upstream and downstream sequences in donor polynucleotide may have about 75%, 76%, 77%, 78%, 79%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% sequence identity with the upstream or downstream sequence of the target sequence. In exemplary embodiments, the upstream and downstream sequences in the donor polynucleotide may have about 95% or 100% sequence identity to the upstream or downstream chromosomal sequence to the sequence targeted by the engineered Cas9 system.

[0068] In some embodiments, the upstream sequence shares substantial sequence identity with the chromosomal sequence located immediately upstream of the sequence targeted by the engineered Cas9 system. In other embodiments, the upstream sequence shares substantial sequence identity with the chromosomal sequence located within about one hundred (100) nucleotides upstream from the target sequence. Thus, for example, the upstream sequence may share substantial sequence identity with the chromosomal sequence located about 1 to about 20, about 21 to about 40, about 41 to about 60, about 61 to about 80, or about 81 to about 100 nucleotides upstream from the target sequence. In some embodiments, the downstream sequence shares substantial sequence identity with the chromosomal sequence located immediately downstream of the sequence targeted by the engineered Cas9 system. In other embodiments, the downstream sequence shares substantial sequence identity with the chromosomal sequence located within about one hundred (100) nucleotides downstream from the target sequence. Thus, for example, the downstream sequence may share substantial sequence identity with a chromosomal sequence located about 1 to about 20, about 21 to about 40, about 41 to about 60, about 61 to about 80, or about 81 to about 100 nucleotides downstream from the target sequence.

[0069] Each upstream or downstream sequence may range in length from about 20 nucleotides to about 5000 nucleotides. In some embodiments, the upstream and downstream sequences may comprise about 50, 100, 200, 300, 400, 500, 600, 700, 800, 900, 1000, 1100, 1200, 1300, 1400, 1500, 1600, 1700, 1800, 1900, 2000, 2100, 2200, 2300, 2400, 2500, 2600, 2800, 3000, 3200, 3400, 3600, 3800, 4000, 4200, 4400, 4600, 4800, or 5000 nucleotides. In certain embodiments, the upstream and downstream sequences may range in length from about 50 to about 1500 nucleotides.

[0070] (c) Cell type A variety of eukaryotic cells are suitable for use in the methods described herein. For example, the cell may be a human cell, a non-human mammalian cell, a non-mammalian vertebrate cell, an invertebrate cell, an insect cell, a plant cell, a yeast cell, or a single-cell eukaryote. In some embodiments, the cell may be a one-cell embryo. For example, non-human mammalian embryos include rat, hamster, rodent, rabbit, cat, dog, sheep, pig, cow, horse, and primate embryos. In still other embodiments, the cell may be a stem cell, such as an embryonic stem cell, an ES-like stem cell, a fetal stem cell, an adult stem cell, and the like. In one embodiment, the stem cell is not a human embryonic stem cell. Additionally, the stem cell may include those made by the techniques described in WO2003 / 046141 or Chung et al. (Cell Stem Cell, 2008, 2:113-117), the contents of which are incorporated herein. The cells may be in vitro (i.e., in culture), ex vivo (i.e., in tissue isolated from an organism), or in vivo (i.e., within an organism). In exemplary embodiments, the cells are mammalian cells or mammalian cell lines. In particular embodiments, the cells are human cells or human cell lines.

[0071] Non-limiting examples of suitable mammalian cells or cell lines include human embryonic kidney cells (HEK293, HEK293T); human cervical carcinoma cells (HELA); human lung cells (W138); human hepatocytes (Hep G2); human U2-OS osteosarcoma cells, human A549 cells, human A-431 cells, and human K562 cells; Chinese hamster ovary (CHO) cells, baby hamster kidney (BHK) cells; mouse myeloma NS0 cells, mouse embryonic fibroblast 3T3 cells (NIH3T3), mouse B lymphoma A20 cells; mouse melanoma B16 cells; mouse myoblast C2C12 cells; mouse myeloma SP2 / 0 cells; mouse embryonic mesenchymal C3H-10T1 / 2 cells; mouse carcinoma CT26 cells. mouse prostate DuCuP cells; mouse mammary EMT6 cells; mouse hepatoma Hepa1c1c7 cells; mouse myeloma J5582 cells; mouse epithelial MTD-1A cells; mouse cardiac MyEnd cells; mouse kidney RenCa cells; mouse pancreatic RIN-5F cells; mouse melanoma X64 cells; mouse lymphoma YAC-1 cells; rat glioblastoma 9L cells; rat B lymphoma RBL cells; rat neuroblastoma B35 cells; rat hepatoma cells (HTC); buffalo rat liver BRL 3A cells; canine kidney cells (MDCK); canine mammary (CMT) cells; rat osteosarcoma D17 cells; rat monocyte / macrophage DH82 cells; monkey kidney SV-40 transformed fibroblast (COS7) cells; monkey kidney CVI-76 cells; African green monkey kidney (VERO-76) cells. An extensive list of mammalian cell lines can be found in the American Type Culture Collection catalog (ATCC, Manassas, VA).

[0072] (V)Applicable The compositions and methods described herein can be used in a variety of therapeutic, diagnostic, industrial, and research applications. In some embodiments, the present disclosure can be used to modify chromosomal sequences of interest in cells, animals, or plants to model and / or study the function of genes, study genetic or epigenetic conditions of interest, or study biochemical pathways involved in various diseases or disorders. For example, transgenic organisms can be created that model diseases or disorders in which the expression of one or more nucleic acid sequences associated with the disease or disorder is altered. Disease models can be used to study the effects of mutations in organisms, study the onset and / or progression of diseases, study the effects of pharmacologic active compounds on diseases, and / or evaluate the effectiveness of potential gene therapy strategies.

[0073] In other embodiments, the compositions and methods can be used to study the function of genes involved in a particular biological process and how changes in gene expression can affect the biological process, perform efficient and cost-effective functional genomic screening, or perform saturating or deep scanning mutagenesis of genomic loci along with cellular phenotypes. Saturating or deep scanning mutagenesis can be used, for example, to determine the critical minimal signature and discrete vulnerability of functional elements required for gene expression, drug resistance, and disease reversal.

[0074] In further embodiments, the compositions and methods described herein can be used for diagnostic testing to establish the presence of a disease or disorder and / or for use in determining treatment options. Examples of suitable diagnostic tests include detection of specific mutations in cancer cells (e.g., specific mutations in EGFR, HER2, etc.), detection of specific mutations associated with specific diseases (e.g., trinucleotide repeats, mutations in β-globulin associated with sickle cell disease, specific SNPs, etc.), detection of hepatitis, detection of viruses (e.g., Zika), etc.

[0075] In further embodiments, the compositions and methods described herein can be used to correct gene mutations associated with a particular disease or disorder, for example, to correct globulin gene mutations associated with sickle cell disease or thalassemia, to correct mutations in the adenosine deaminase gene associated with severe combined immunodeficiency (SCID), to reduce expression of HTT, the gene responsible for Huntington's disease, or to correct mutations in the rhodopsin gene for the treatment of retinitis pigmentosa. Such modifications may be made in cells ex vivo.

[0076] In yet another aspect, the compositions and methods described herein can be used to generate crop plants with improved characteristics or increased resistance to environmental stress. The present disclosure can also be used to generate livestock or production animals with improved characteristics. For example, pigs have many features that make them attractive as biomedical models, especially in regenerative medicine or xenotransplantation.

[0077] definition Unless otherwise defined, all technical and scientific terms used herein have the meanings commonly understood by those skilled in the art to which this invention belongs. The following references provide those skilled in the art with general definitions of many terms used in this invention: Singleton et al., Dictionary of Microbiology and Molecular Biology (2nd Ed. 1994); The Cambridge Dictionary of Science and Technology (Walker ed., 1988); The Glossary of Genetics, 5th Ed., R. Rieger et al. (eds.), Springer Verlag (1991); and Hale & Marham, The Harper Collins Dictionary of Biology (1991). The following terms used herein have the meanings ascribed to them unless otherwise specified.

[0078] When introducing elements of the present disclosure or preferred embodiments thereof, the articles "a," "an," "the," and "said" are intended to mean that there are one or more of the element. The terms "comprising," "containing," and "having" are intended to be inclusive and mean that there may be additional elements other than the listed elements.

[0079] The term "about" when used in reference to a numerical value, e.g., x, means x±5%.

[0080] The term "complementary" or "complementarity" as used herein refers to the association of double-stranded nucleic acids by base pairing through specific hydrogen bonds. Base pairing can be standard Watson-Crick base pairing (e.g., 5'-AGT C-3' pairs with the complementary sequence 3'-TCA G-5'). Base pairing can also be Hoogsteen or reverse Hoogsteen hydrogen bonding. Complementarity is typically measured over the double-stranded region, thus excluding, for example, overhangs. Complementarity between two strands of a double-stranded region can be partial and expressed as a percentage (e.g., 70%) when only a portion (e.g., 70%) of the bases are complementary. Non-complementary bases are "mismatched". Complementarity can also be complete (i.e., 100%) when all bases in the double-stranded region are complementary.

[0081] As used herein, the term "CRISPR / Cas system" or "Cas9 system" refers to a complex that includes a Cas9 protein (i.e., a nuclease, nickase, or catalytically inactive protein) and a guide RNA.

[0082] As used herein, the term "endogenous sequence" refers to a chromosomal sequence that is native to a cell.

[0083] The term "exogenous" as used herein refers to a sequence that is not native to the cell or a chromosomal sequence that is at a chromosomal location that differs from its natural location in the genome of the cell.

[0084] As used herein, "gene" refers to a DNA region (including exons and introns) that encodes a gene product, as well as all DNA regions that regulate the production of the gene product, whether or not regulatory sequences flank the coding and / or transcribed sequence. Thus, a gene includes, but is not necessarily limited to, promoter sequences, terminators, translational regulatory sequences, such as ribosome binding sites and internal ribosome entry sites, enhancers, silencers, insulators, boundary elements, origins of replication, matrix attachment sites, and locus control regions.

[0085] The term "heterologous" refers to an entity that is not endogenous or native to a cell of interest. For example, a heterologous protein refers to a protein that is derived or originally derived from an exogenous source, such as an exogenously introduced nucleic acid sequence. In some cases, a heterologous protein may be a protein that is not normally produced by the cell of interest.

[0086] The term "nickase" refers to an enzyme that cleaves one strand of a double-stranded nucleic acid sequence (i.e., nicks the double-stranded sequence). For example, a nuclease with double-strand cleavage activity may be modified by mutation and / or deletion so that it functions as a nickase and cleaves only one strand of a double-stranded sequence.

[0087] The term "nuclease" as used herein refers to an enzyme that cleaves both strands of a double-stranded nucleic acid sequence.

[0088] The terms "nucleic acid" and "polynucleotide" refer to deoxyribonucleotide or ribonucleotide polymers in linear or circular structures and in either single- or double-stranded form. For the purposes of this disclosure, these terms should not be construed as limiting on the length of the polymer. The terms may include known analogs of natural nucleotides, as well as nucleotides that are modified at the base, sugar, and / or phosphate moieties (e.g., phosphorothioate backbones). In general, analogs of a particular nucleotide have the same base-pairing specificity; i.e., an analog of A will base pair with T.

[0089] The term "nucleotide" refers to deoxyribonucleotides or ribonucleotides. A nucleotide may be a standard nucleotide (i.e., adenosine, guanosine, cytidine, thymidine, and uridine), a nucleotide isomer, or a nucleotide analog. A nucleotide analog refers to a nucleotide with a modified purine or pyrimidine base or a modified ribose moiety. A nucleotide analog may be a natural nucleotide (e.g., inosine, pseudouridine, etc.) or a non-natural nucleotide. Non-limiting examples of modifications in the sugar or base portion of a nucleotide include the addition (or removal) of acetyl, amino, carboxyl, carboxymethyl, hydroxyl, methyl, phosphoryl, and thiol groups, and the replacement of carbon and nitrogen atoms of the base with other atoms (e.g., 7-deazapurines). Nucleotide analogs also include dideoxynucleotides, 2'-O-methyl nucleotides, locked nucleic acids (LNA), peptide nucleic acids (PNA), and morpholinos.

[0090] The terms "polypeptide" and "protein" are used interchangeably to refer to a polymer of amino acid residues.

[0091] The terms "target sequence," "target chromosomal sequence," and "target site" are used interchangeably to refer to a specific sequence in chromosomal DNA that is targeted by an engineered Cas9 system and the site at which the engineered Cas9 system modifies the DNA or a protein associated with the DNA.

[0092] Techniques for determining nucleic acid and amino acid sequence identity are known in the art. Typically, such techniques involve determining the nucleotide sequence of the mRNA for a gene and / or determining the amino acid sequence encoded thereby, and comparing these sequences with a second nucleotide or amino acid sequence. Genomic sequences may also be determined and compared in this manner. In general, identity refers to the exact nucleotide-to-nucleotide or amino acid-to-amino acid correspondence of two polynucleotide or polypeptide sequences, respectively. Two or more sequences (polynucleotide or amino acid) may be compared by determining their percent identity. The percent identity of two sequences, whether nucleic acid or amino acid sequences, is the number of exact matches between the two aligned sequences divided by the length of the shorter sequence, multiplied by 100. Approximate alignment of nucleic acid sequences is provided by the local homology algorithm of Smith and Waterman, Advances in Applied Mathematics 2:482-489 (1981). This algorithm can be applied to amino acid sequences by using a scoring matrix developed by Dayhoff, Atlas of Protein Sequences and Structure, MO Dayhoff ed., 5 suppl. 3:353-358, National Biomedical Research Foundation, Washington, DC, USA, and normalized by Gribskov, Nucl. Acids Res. 14(6):6745-6763 (1986). An exemplary implementation of this algorithm for determining percent identity of sequences is provided by Genetics Computer Group (Madison, Wis.) in the "BestFit" utility application. Other suitable programs for calculating percent identity or similarity between sequences are generally known in the art, for example, another alignment program is BLAST, used with default parameters.For example, BLASTN and BLASTP can be used using the following default parameters: genetic code=standard; filter=none; strand=both; cutoff=60; expect=10; Matrix=BLOSUM62; Descriptions=50 sequences; sort by=HIGH SCORE; Databases=non-redundant, GenBank+EMBL+DDBJ+PDB+GenBank CDS translations+Swiss protein+Spupdate+PIR. Details of these programs can be found on the GenBank website.

[0093] Since various modifications can be made in the cells and methods described above without departing from the scope of the present invention, it is intended that all matter contained in the above description and in the examples which follow be interpreted as illustrative and not in a limiting sense. EXAMPLES

[0094] Working Example The following examples illustrate certain aspects of the present disclosure.

[0095] Example 1: Determining the PAM requirements for targeted DNA cleavage by Cas9 orthologs Cas9 orthologues from Bacillus smithii, Lactobacillus rhamnosus, Parasatellella exclementihominis, Mycoplasma canis, Mycoplasma gallisepticum, Akkermansia glycaniphila, Akkermansia muciniphila, Oenococcus kitaharae, Bifidobacterium bombyi, Acidothermus cellulolyticus, Alicyclobacillus hesperidum, Wallinella succinogenes, Nitratiphracter sarusginis, Ralstonia szygii, and Corynebacterium diphtheriae were optimized for expression in human cells and codon tagged with the SV40 large T-antigen nuclear localization sequence (NLS) at the C-terminus (SEQ ID NOs: 1-30; see Table 6 below). Expression of each orthologue was driven by the human cytomegalovirus (CMV) immediate early enhancer and promoter. CRISPR RNA (crRNA) and putative trans-activating crRNA (tracrRNA) for each ortholog were joined together to form a single guide RNA (sgRNA) (SEQ ID NO: 31-45; see Table 6 below). Expression of each sgRNA was driven by the human U6 promoter. In vitro transcribed sgRNAs were prepared from T7 promoter-tagged PCR templates as a supplement for in vitro digestion.

[0096] Human K562 cells were transfected with Cas9-encoding plasmid and sgRNA-expressing plasmid by nucleofection. Each transfection consisted of 2 million cells, 5 μg of Cas9-encoding plasmid DNA, and 3 μg of sgRNA-expressing plasmid DNA. Cells were harvested approximately 24 hours after transfection, washed with ice-cold PBS buffer, and lysed in 150 μL of lysis solution (20 mM HEPES, pH 7.5; 100 mM KCl; 5 mM MgCl2, 1 mM DTT, 5% glycerol, 0.1% Triton X-100, 1x protease inhibitor) with constant stirring for 30 min in a 4 °C cold room. Supernatants were prepared by centrifugation at 16,000 x g for 2 min at 4 °C to remove residual cell debris and were used as a source of Cas9 RNP for in vitro digestion of the plasmid DNA PAM library. The library consisted of 4 nucleotides, each immediately preceded by a protospacer in the following configuration: 5'-GTACAAACGGCAGAAGCTGGNNNNNNNN-3' (SEQ ID NO:46). 8 Each in vitro digestion contained 10 μL of cell lysate supernatant, 2 μL of 5x digestion buffer (100 mM HEPES, pH 7.5; 500 mM KCl; 25 mM MgCl) in a 20 μL reaction volume. 2 ; 5 mM DTT; 25% glycerol), 800 ng of PAM library DNA, and 20 pmol of in vitro transcribed sgRNA supplement. The reaction was maintained at 37 °C for 30 min and then purified with a PCR purification kit. Illumina NextSeq sequencing libraries were prepared from the digested products and subjected to deep sequencing. Deep sequencing data was analyzed using the Weblogo program to infer the PAM requirements for each Cas9 ortholog.

[0097] The results are summarized in Figure 1. The results revealed several Cas9 orthologs that use A and / or T containing PAMs for in vitro targeted DNA cleavage. These Cas9 orthologs could provide a means to target AT-rich genomic sites. The results also revealed several Cas9 orthologs that use suitable PAMs to target GC-rich genomic sites. These Cas9 orthologs could provide an alternative targeting scheme for SpyCas9 at GC-rich genomic sites and improve targeting resolution and specificity.

[0098] Example 2: Genome modification using Bacillus smithii Cas9 (BsmCas9) and Lactobacillus rhamnosus Cas9 (LrhCas9) As shown in Figure 1 and Table A (above), small BsmCas9 (1095aa) (SEQ ID NO:2) and LrhCas9 (SEQ ID NO:4) use 5'-NNNNCAAA-3'PAM and 5'-NGAAA-3'PAM, respectively, for target DNA binding. The use of these novel PAMs provides a means to target AT-rich genomic sites. To demonstrate gene editing, human K562 cells (1x10 6 ) were nucleofected with 5 μg of Cas9-encoding plasmid DNA and 3 μg of sgRNA-expressing plasmid DNA. Targeted genomic sites included the human tyrosine-protein phosphatase nonreceptor type 2 (PTN2) locus, the human empty spiracles homeobox 1 (EMX1) locus, the human programmed cell death 1 ligand 1 (PD1L1) locus, the human AAVS1 safe harbor locus, the human cytochrome p450 oxidoreductase (POR) locus, and the human nuclear receptor subfamily 1 group I member 3 (CAR) locus. Genomic DNA was extracted with DNA extraction solution (QuickExtract) 3 days after transfection. TM ) and the targeted genomic regions were PCR amplified using JumpStart Taq TM ReadyMix TM ). PCR primers are listed in Table 1. [Table 1]

[0099] Amplification was performed using the following conditions: 2 min cycles at 98°C for initial denaturation; 34 cycles of 15 s at 98°C, 30 s at 62°C, and 45 s at 72°C; 5 min cycles at 72°C; and hold at 4°C. PCR products were digested with Cel-1 nuclease and resolved on 10% acrylamide gels. Targeted mutation rates were measured using ImageJ and presented as percent insertions and / or deletions (% indels). Results are summarized in Table 2. These results demonstrate that both Cas9 orthologs were able to edit endogenous genomic sites in human cells using 5'-NNNNCAAA-3'PAM (BsmCas9) or 5'-NGAAA-3'PAM (LrhCas9). [Table 2]

[0100] Example 3: Improvement of Parasatellella exclementihominis Cas9 (PexCas9) by fusion with chromatin regulatory motifs Parasatellella exclementihominis Cas9 (PexCas9-NLS) (SEQ ID NO: 6) was modified by fusion with the human HMGN1 peptide (SEQ ID NO: 72) at the N-terminus using a TGSG linker (SEQ ID NO: 109) and either the human HMGB1 box A peptide (PexCas9-HN1HB1 fusion; SEQ ID NO: 117) or the human histone H1 middle globular domain peptide (PexCas9-HN1H1G; SEQ ID NO: 118) at the C-terminus using a LEGGGS linker (SEQ ID NO: 108). [Table 3]

[0101] Human K562 cells (1x10 6 ) were transfected with plasmid DNA encoding PexCas9-NLS, PexCas9-HN1HB1 fusion, or PexCas9-HN1H1G fusion at molar equivalents (5 and 5.4 μg, respectively) and 3 μg of sgRNA plasmid to target a genomic site at the human cytochrome p450 oxidoreductase (POR) locus. Genomic DNA was extracted 3 days after transfection using DNA extraction solution (QuickExtract TM ), and the targeted genomic region was PCR amplified using forward primer 5'-CTCCCCTGCTTCTTGTCGTAT-3' (SEQ ID NO:55) and reverse primer 5'-ACAGGTCGTGGACACTCACA-3' (SEQ ID NO:56). Amplification was performed using the following conditions: 2 min cycle at 98°C for initial denaturation; 34 cycles of 15 sec at 98°C, 30 sec at 62°C, and 45 sec at 72°C; 5 min cycle at 72°C; and hold at 4°C. PCR products were digested with Cel-1 nuclease and resolved on 10% acrylamide gel. Targeted mutation rates were measured using ImageJ and presented as percent insertions and / or deletions (% indels). The results are summarized in Table 4. The results demonstrate that Cas9 fusions with at least one chromatin regulatory motif enhance its gene editing efficiency against endogenous targets in human cells. [Table 4] *PAM determinant nucleotides are underlined.

[0102] Example 4. Improvement of the Mycoplasma canis Cas9 (McaCas9) system by sgRNA modification The wild-type crRNA coding sequence of McaCas9 contains four consecutive thymidine residues in the repeat region, and three of the four thymidine residues are expected to pair with three adenosine residues in the putative tracrRNA sequence when the crRNA and tracrRNA are bound together to form the sgRNA. Human RNA polymerase (Pol) III is known to use four or more consecutive thymidine residues on the coding RNA strand as a transcription termination signal. To prevent premature transcription termination of the McaCas9 sgRNA in human cells, a T to C mutation and a corresponding A to G mutation were introduced into the sgRNA scaffold to form a modified sgRNA scaffold with the following sequence: 5'-GUU C UAGUGUUGUACAAUAUUUGGGUGAAAACCCAAAUAUUGUACAUCCUA G AUCAAGGCGCUUAAUUGCUGCCGUAAUUGCUGAAAGCGUAGCUUUCAGUUUUUUU-3' (SEQ ID NO: 76), where the mutated nucleotides are underlined. This modification was also expected to increase the thermodynamic stability of the sgRNA scaffold.

[0103] Human K562 cells (1x10 6 ) were transfected with 5.5 μg of plasmid DNA encoding an McaCas9 fusion protein containing an HMGN1 peptide on the N-terminus and a histone H1 globular domain peptide on the C-terminus, and 3 μg of sgRNA plasmid DNA encoding a control sgRNA scaffold or a modified sgRNA scaffold. Genomic DNA was extracted 3 days after transfection using DNA extraction solution (QuickExtract TM), and the targeted genomic region was PCR amplified using forward primer 5'-CTCCCCTGCTTCTTGTCGTAT-3' (SEQ ID NO:55) and reverse primer 5'-ACAGGTCGTGGACACTCACA-3' (SEQ ID NO:56). Amplification was performed using the following conditions: 2 min cycle at 98°C for initial denaturation; 34 cycles of 15 sec at 98°C, 30 sec at 62°C, and 45 sec at 72°C; 5 min cycle at 72°C; and hold at 4°C. PCR products were digested with Cel-1 nuclease and resolved on a 10% acrylamide gel. Targeted mutation rates were measured using ImageJ and presented as percent insertions and / or deletions (% indels). The results are summarized in Table 5. The results demonstrate that the activity of Cas9 orthologs in mammalian cells can be enhanced by modifying their sgRNA scaffolds. [Table 5] *PAM determinant nucleotides are underlined.

[0104] Example 5. Improved McaCas9, BsmCas9, PexCas9, and LrhCas9 activity by fusion with chromatin regulatory motifs Additional Cas9-CMM fusion proteins were prepared by linking the McaCas9-NLS, BsmCas9-NLS, and LrhCas9-NLS proteins to HMGN1 (HN1) at the amino terminus and either HMGB1 box A (HB1) or histone H1 central globular motif (H1G) at the carboxyl terminus to produce McaCas9-HN1HB1 (SEQ ID NO: 123), McaCas9-HN1H1G (SEQ ID NO: 124), BsmCas9-HN1HB1 (SEQ ID NO: 119), Bsm-HN1H1G (SEQ ID NO: 120), Lrh-HN1HB1 (SEQ ID NO: 121), LrhCas9-HN1H1G (SEQ ID NO: 122). The nuclease activities of these fusions and the PexCas9-CMM fusion described above in Example 3 were compared to the activities of the corresponding engineered Cas9 proteins essentially as described above in Examples 2 and 3. Table 6 shows the target sites (i.e., protospacer+PAM, shown in bold with critical nucleotides underlined) at specific loci for each Cas9 nuclease. [Table 6]

[0105] The percent of indels under each condition is plotted in Figure 2A-D. Both HN1HB1 and HN1H1G combinations significantly enhanced the four Cas9 orthologs at at least one site. Based on the magnitude of fold change, the CMM fusion modification provided the greatest enhancement for McaCas9, increasing its activity at least 5-fold at two sites tested (Figure 2A). CMM fusions provided more than 2-fold enhancement for PexCas9 (Figure 2B). BsmCas9 activity was enhanced more than 3-fold at one site, but only by a 20% increase at the second site, and had no effect at the third site (Figure 2C). It should be noted, however, that all three BsmCas9 nucleases were highly efficient (>35% indels). LrhCas9 was highly efficient at two sites tested (22% and 33% indels) even without fusion modification (Figure 2D). However, the HN1H1G combination still provided significant enhancement for both sites, with 70% and 28% increases in activity. These results demonstrate that the CMM fusion strategy enhances gene editing efficiency.

[0106] Example 6. Off-target effects of Cas9-CMM fusions To assess the off-target activity of Cas9-CMM fusions, one to five of the top ranked potential off-target sites for each target site were analyzed using the Surveyor Nuclease assay. In addition to the Cas9 and Cas9-CMM fusion data described above in Example 5, data from Streptococcus pyogenes Cas9 (SpyCas9), SpyCas9-CMM fusions, Streptococcus pasteurianus Cas9 (SpaCas9), Spa-CMM fusions, Campylobacter jejuni Cas9 (CjeCas9), and CjeCas9-SMM fusions were also analyzed. From a total of 64 potential off-target sites assayed, off-target cleavage was detected at 11 sites contributed by 9 guide sequences out of a total of 21 guide sequences tested. At 11 off-target sites, control Cas9 and fusion nuclease were simultaneously present, except for the POR Spy 1-OT1 site, where no off-target cleavage was detected in control SpyCas9. In general, there were no significant differences between fusion nuclease and control Cas9 (Figure 3). For example, across all 11 off-target sites, HN1H1G fusion combinations averaged 8.0±6.0% indels, while control Cas9 averaged 7.5±5.1% indels. Similarly, across the 10 off-target sites associated with the HN1HB1 fusion combination, there were no significant differences between the fusion combination and control Cas9 (6.9±5.7% vs. 6.5±5.4% indels). Taken together, these results indicate that on-target activity enhancement by HN1H1B and HN1H1G fusion combinations does not generally result in an increase in off-target activity.

[0107] Engineered Cas9 Systems Table 7 shows the human codon-optimized DNA and protein sequences of engineered Cas9 / NLS proteins (SEQ ID NOs: 1-30, where the NLS sequence is underlined) and DNA sequences of engineered sgRNAs (SEQ ID NOs: 31-45; the N residue at the 5' end indicates the programmable target sequence). Cas9-CMM fusions (SEQ ID NOs: 117-124) are also shown. [Table 7-1] [Table 7-2] [Table 7-3] [Table 7-4] [Table 7-5] [Table 7-6] [Table 7-7] [Table 7-8] [Table 7-9] [Table 7-10] [Table 7-11]

Table 7-12

Table 7-13

Table 7-14

Table 7-15

Table 7-16

Table 7-17

Table 7-18

Table 7-19

Table 7-20

Table 7-21

Table 7-22

Table 7-23

Table 7-24

Table 7-25

Table 7-26

Table 7-27

Table 7-28

Table 7-29

Table 7-30

Table 7-31

Table 7-32

Table 7-33

Table 7-34

Claims

[Claim 1] The invention described in the specification or drawings of this application.

Images