Epigenetic editing tool for targeting hepatitis b virus gene

Abstract

The present application relates to the field of biomedicine, and provides an epigenetic editing tool for targeting a hepatitis B virus gene and a use thereof.

Description

Epigenetic editing tools targeting hepatitis B virus genes Technical Field

[0001] The present application relates to the field of biomedicine, and specifically to a target-specific epigenetic editing tool and its use. Background Art

[0002] Hepatitis B virus (HBV) is a hepatotropic DNA virus. Chronic infection with HBV can lead to persistent liver inflammation, significantly increasing the risk of cirrhosis and liver cancer. The World Health Organization (WHO) estimates that there are currently over 250 million cases of chronic hepatitis B worldwide, resulting in over 800,000 deaths annually, placing a significant burden on global public health. China, a populous country, accounts for approximately one-third of the world's hepatitis B carriers. Since the 1980s, with the increase in hepatitis B vaccination rates, new cases of HBV in my country have been effectively controlled. However, the number of HBV infections in China remains substantial.

[0003] Current HBV treatments, such as nucleoside (acid) analogs and interferon (IFN), can effectively inhibit viral replication. However, achieving a functional cure—that is, reducing surface antigen (HBsAg) to undetectable levels—is difficult, and long-term medication is required. Once treatment is discontinued, HBV replication rebounds. This phenomenon is primarily due to the formation of covalently closed circular DNA (cccDNA) after HBV infection of hepatocytes. The HBV genome can integrate into the host hepatocyte genome. Both cccDNA and integrated DNA serve as stable templates for viral replication and protein expression over the long term, and current conventional treatments do not eliminate them. Therefore, eliminating or silencing cccDNA and integrated DNA may be effective in treating HBV infection. Because cccDNA can assemble with histones in the host hepatocyte nucleus to form a chromosome-like structure, its transcriptional regulation can also be influenced by epigenetic modifications. The HBV genome contains three CpG islands, referred to hereafter as CGI, CGI II, and CGI III. CpG islands are key regions for epigenetic regulation. The transcription of the HBV genome is regulated by four promoters (Xp, Cp, Sp1, Sp2) and two enhancers (Enh I and Enh II), among which Xp, Cp, Enh I and Enh II are located in the CG II region, and Sp1 and Sp2 are located near CG I and CG III. Therefore, epigenetic editing of CpG islands may affect multiple regulatory elements, thereby affecting the transcription of the viral genome.

[0004] Introducing epigenetic modifications into specific regulatory regions or sites within the HBV genome can alter chromatin structure, thereby shifting the target gene into a transcriptionally repressed state and achieving silencing regulation. This process avoids DNA cleavage, preventing the possibility of double-strand breaks in the genome and fundamentally eliminating the risk of activating unpredictable DNA repair mechanisms and potentially producing immunogenic truncated or mutant proteins. However, research on epigenetic editing tools specifically targeting the HBV genome is largely in its early stages, and the development of epigenetic editing technologies capable of sustainably curing or eliminating HBV virus faces many challenges, including unknowns and limitations.

[0005] Summary of the Invention

[0006] This application aims to develop a safe and effective therapy for silencing and regulating HBV target genes. It provides a method for introducing inhibitory epigenetic modifications in specific regulatory regions of the HBV genome through epigenetic editing tools, thereby changing the transcriptional activity of hepatitis B virus cccDNA and integrated genomic DNA, thereby reducing HBV replication and protein expression, and achieving the purpose of treating hepatitis B.

[0007] On the one hand, the present application provides a composition comprising: (1) a fusion molecule or a nucleic acid sequence encoding the fusion molecule, wherein the fusion molecule comprises at least one DNA binding protein and at least one gene expression regulator, and (2) at least one single guide RNA (sgRNA), or a nucleic acid sequence encoding the sgRNA, wherein the sgRNA is complementary to a target DNA sequence near a hepatitis B virus (HBV) gene and / or within an HBV gene regulatory element, wherein the HBV gene is a type B HBV gene comprising the nucleotide sequence shown in SEQ ID NO: 1, a type C HBV gene comprising the nucleotide sequence shown in SEQ ID NO: 2, or a type C HBV gene comprising the nucleotide sequence shown in SEQ ID NO: 3. NO:3 shows a D-type HBV gene having a nucleotide sequence, wherein the HBV gene regulatory elements include a transcription start site, a core promoter, a promoter, an enhancer, a silencer, an insulator element, a boundary element and / or a locus control region, and the target DNA sequence is located between nucleotides 1056 and 2354, between nucleotides 2639 and 2658, between nucleotides 2863 and 2930, and / or between nucleotides 3048 and 3067 of the HBV gene.

[0008] In certain embodiments, the target DNA sequence is located between nucleotides 1056 and 1900, between nucleotides 1972 and 2082, between nucleotides 2134 and 2264, between nucleotides 2335 and 2354, between nucleotides 2639 and 2658, between nucleotides 2863 and 2930, and / or between nucleotides 3048 and 3067 of the HBV gene.

[0009] In certain embodiments, the target DNA sequence is located between nucleotides 1060 to 1079, between nucleotides 1149 to 1612, between nucleotides 1693 to 1852, and / or between nucleotides 2863 to 2882 of the HBV gene.

[0010] In certain embodiments, the target DNA sequence is located in one or more regions of the following type B HBV gene: between nucleotides 1149 and 1190, between nucleotides 1210 and 1310, between nucleotides 1350 and 1400, between nucleotides 1420 and 1450, and between nucleotides 1470 and 1592.

[0011] In certain embodiments, the target DNA sequence is located in one or more regions of the following type C HBV gene: between nucleotides 1150 and 1180, between nucleotides 1200 and 1310, between nucleotides 1350 and 1390, between nucleotides 1420 and 1460, and between nucleotides 1480 and 1593.

[0012] In certain embodiments, the target DNA sequence is located in one or more regions of the following D-type HBV gene: between nucleotides 1056 and 1079, between nucleotides 1101 and 1900, between nucleotides 1972 and 2082, between nucleotides 2134 and 2264, between nucleotides 2335 and 2354, between nucleotides 2639 and 2658, between nucleotides 2863 and 2882, between nucleotides 2911 and 2930, and between nucleotides 3048 and 3067.

[0013] In certain embodiments, the target DNA sequence is located in one or more regions of the following D-type HBV gene: between nucleotides 1060 and 1079, between nucleotides 1160 and 1310, between nucleotides 1253 and 1284, between nucleotides 1370 and 1470, between nucleotides 1490 and 1612, between nucleotides 1693 and 1852, and between nucleotides 2863 and 2882.

[0014] For example, the sequence of the complete genome of type B HBV (serotype adw) is as follows:

[0015] For example, the sequence of the complete genome of type C HBV (serotype adr) is as follows:

[0016] For example, the sequence of the D-type HBV (serotype ayw) full genome is as follows:

[0017] In certain embodiments, the sgRNA comprises the nucleotide sequence shown in any one of SEQ ID NOs: 4-1165.

[0018] In certain embodiments, the sgRNA comprises a partial sequence of the nucleotide sequence shown in any one of SEQ ID NOs: 4-1165, and the length of the partial sequence is 15-20 base pairs.

[0019] In certain embodiments, the at least one DNA binding protein is a CRISPR enzyme, a zinc finger nuclease (ZNF), a transcription activator-like effector nuclease (TALEN), a homing endonuclease, a dCas9-FokI nuclease, or a MegaTal nuclease.

[0020] In certain embodiments, the CRISPR enzyme is a Class 2 Cas protein and / or a mutant thereof.

[0021] In certain embodiments, the CRISPR enzyme is one or more Cas proteins described below: class 2 type II-A Cas protein, class 2 type II-B Cas protein, class 2 type II-C Cas protein, class 2 type VA Cas protein, class 2 type VB Cas protein, class 2 type VC Cas protein, class 2 type VU Cas protein, and mutants thereof.

[0022] In certain embodiments, the CRISPR enzyme is a Cas9 protein and / or a mutant thereof.

[0023] In certain embodiments, the at least one DNA binding protein is dCas9.

[0024] In certain embodiments, the dCas9 comprises Staphylococcus aureus dCas9, Streptococcus pyogenes dCas9, Campylobacter jejuni dCas9, Corynebacterium diphtheria dCas9, Eubacterium ventriosum dCas9, Streptococcus pasteurianus dCas9, Lactobacillus farciminis dCas9, Sphaerochaeta globus dCas9, Azospirillum (e.g., strain B510) dCas9, Gluconacetobacter diazotrophicus dCas9, Neisseria cinerea dCas9, Roseburia enterica serovar Typhimurium dCas9, and the like. intestinalis) dCas9, Parvibaculum lavamentivorans) dCas9, Nitratifractor salsuginis (e.g., strain DSM 16511) dCas9, Campylobacter lari (e.g., strain CF89-12) dCas9, Streptococcus thermophilus (e.g., strain LMD-9) dCas9.

[0025] In certain embodiments, the dCas9 comprises the amino acid sequence shown in SEQ ID NOs: 1170-1187.

[0026] In certain embodiments, the at least one gene expression regulator provides for modification of at least one nucleotide adjacent to the HBV gene and / or within a regulatory element of the HBV gene.

[0027] In certain embodiments, the at least one gene expression regulator comprises one or more selected from the group consisting of DNA methyltransferases, DNA hydroxymethylases, DNA demethylases, histone methyltransferases, histone demethylases, histone acetyltransferases, histone deacetylases, phosphatases, kinases, transcriptional activators, transcriptional repressors, portions thereof, and any combination thereof.

[0028] In certain embodiments, the modification of the at least one nucleotide is DNA methylation.

[0029] In certain embodiments, the at least one gene expression regulator comprises one or more selected from the group consisting of DNA methyltransferases (DNMTs), zinc finger protein-based transcription factors, moieties described above, and any combination thereof.

[0030] In certain embodiments, the at least one gene expression regulator comprises a DNA methyltransferase (DNMT) or a portion thereof, and a zinc finger protein-based transcription factor or a portion thereof.

[0031] In certain embodiments, the DNA methyltransferase is DNMT3A, DNMT3B, DNMT3L, DNMT1, or DNMT2.

[0032] In certain embodiments, the DNMT3A comprises the amino acid sequence shown in SEQ ID NO: 1166, and the DNMT3L comprises the amino acid sequence shown in SEQ ID NO: 1167 or 1195.

[0033] In certain embodiments, the zinc finger protein-based transcription factor is Krüppel-related repressor (KRAB) or a KRAB domain derived from ZIM3 (ZIM3 KRAB).

[0034] In certain embodiments, the zinc finger protein-based transcription factor comprises the amino acid sequence shown in SEQ ID NO: 1168 or 1196.

[0035] In certain embodiments, the DNA methyltransferase is selected from DNMT3A and DNMT3L, and combinations thereof, and the zinc finger protein-based transcription factor is KRAB or ZIM3 KRAB.

[0036] In certain embodiments, the fusion molecule comprises the at least one gene expression regulator fused to the C-terminus, N-terminus, or both of the at least one DNA binding protein.

[0037] In certain embodiments, the at least one gene expression regulator is directly fused to the at least one DNA binding protein.

[0038] In certain embodiments, the at least one gene expression regulator is indirectly fused to the at least one DNA binding protein via a non-regulatory agent, a second regulator, or a linker.

[0039] In certain embodiments, the fusion molecule comprises the domain DNMT3A-DNMT3L-dCas9-KRAB or the domain DNMT3A-DNMT3L-ZIM3 KRAB-dCas9, wherein - indicates that the partial domains of the fusion molecule are directly and / or indirectly connected, and the partial domains are in order from N-terminus to C-terminus.

[0040] In certain embodiments, the fusion molecule comprises the amino acid sequence shown in SEQ ID NO: 1169 or 1194.

[0041] In certain embodiments, the fusion molecule further comprises at least one nuclear localization sequence (NLS).

[0042] In certain embodiments, the at least one nuclear localization sequence is fused directly or indirectly to the C-terminus, N-terminus, or both of the at least one DNA binding protein.

[0043] In certain embodiments, the nucleic acid sequence encoding the fusion molecule is deoxyribonucleic acid (DNA) or messenger ribonucleic acid (mRNA).

[0044] In certain embodiments, the fusion molecule is packaged in a liposome or lipid nanoparticle.

[0045] In certain embodiments, the fusion molecule and the sgRNA are packaged in liposomes or lipid nanoparticles.

[0046] In certain embodiments, the fusion molecule and the sgRNA are packaged in the same liposome or lipid nanoparticle, or in different liposomes or lipid nanoparticles.

[0047] In certain embodiments, the liposome or the lipid nanoparticle comprises ionizable lipid (20%-70%, molar ratio), PEGylated lipid (0%-30%, molar ratio), supporting lipid (30%-50%, molar ratio) and cholesterol (10%-50%, molar ratio).

[0048] In certain embodiments, the ionizable lipid is selected from a pH-responsive ionizable lipid, a heat-responsive ionizable lipid, and a light-responsive ionizable lipid.

[0049] In certain embodiments, the fusion molecule is packaged in an AAV vector.

[0050] In certain embodiments, the fusion molecule and the sgRNA are packaged in an AAV vector.

[0051] In certain embodiments, the fusion molecule and the sgRNA are packaged in the same AAV vector or different AAV vectors.

[0052] In certain embodiments, the composition is a pharmaceutical composition comprising a pharmaceutically acceptable carrier.

[0053] On the other hand, the present application provides a single guide RNA (sgRNA), wherein the sgRNA comprises a sequence complementary to a target DNA sequence, wherein the target DNA sequence is located near a hepatitis B virus (HBV) gene and / or within an HBV gene regulatory element; the HBV gene is a type B HBV gene comprising the nucleotide sequence shown in SEQ ID NO: 1, a type C HBV gene comprising the nucleotide sequence shown in SEQ ID NO: 2, or a type D HBV gene comprising the nucleotide sequence shown in SEQ ID NO: 3, and the HBV gene regulatory element comprises a transcription start site, a core promoter, a promoter, an enhancer, a silencer, an insulator element, a boundary element and / or a locus control region, and the target DNA sequence is located between nucleotides 1056 and 2354, between nucleotides 2639 and 2658, between nucleotides 2863 and 2930, and / or between nucleotides 3048 and 3067 of the HBV gene.

[0054] In certain embodiments, the target DNA sequence is located between nucleotides 1056 and 1900, between nucleotides 1972 and 2082, between nucleotides 2134 and 2264, between nucleotides 2335 and 2354, between nucleotides 2639 and 2658, between nucleotides 2863 and 2930, and / or between nucleotides 3048 and 3067 of the HBV gene.

[0055] In certain embodiments, the target DNA sequence is located between nucleotides 1060 and 1079, between nucleotides 1149 and 1612, between nucleotides 1693 and 1852, and / or between nucleotides 2863 and 2882 of the HBV gene.

[0056] In certain embodiments, the target DNA sequence is located in one or more regions of the following type B HBV gene: between nucleotides 1149 and 1190, between nucleotides 1210 and 1310, between nucleotides 1350 and 1400, between nucleotides 1420 and 1450, and between nucleotides 1470 and 1592.

[0057] In certain embodiments, the target DNA sequence is located in one or more regions of the following type C HBV gene: between nucleotides 1150 and 1180, between nucleotides 1200 and 1310, between nucleotides 1350 and 1390, between nucleotides 1420 and 1460, and between nucleotides 1480 and 1593.

[0058] In certain embodiments, the target DNA sequence is located in one or more regions of the following D-type HBV gene: between nucleotides 1056 and 1079, between nucleotides 1101 and 1900, between nucleotides 1972 and 2082, between nucleotides 2134 and 2264, between nucleotides 2335 and 2354, between nucleotides 2639 and 2658, between nucleotides 2863 and 2882, between nucleotides 2911 and 2930, and between nucleotides 3048 and 3067.

[0059] In certain embodiments, the target DNA sequence is located in one or more of the following regions of the D-type HBV gene: between nucleotides 1060 and 1079, between nucleotides 1160 and 1310, between nucleotides 1253 and 1284, between nucleotides 1370 and 1470, between nucleotides 1490 and 1612, between nucleotides 1693 and 1852, and between nucleotides 2863 and 2882.

[0060] In certain embodiments, the sgRNA comprises the nucleotide sequence shown in any one of SEQ ID NOs: 4-1165.

[0061] In certain embodiments, the sgRNA comprises a partial sequence of the nucleotide sequence shown in any one of SEQ ID NOs: 4-1165, and the length of the partial sequence is 15-20 base pairs.

[0062] On the other hand, the present application provides a nucleic acid molecule encoding the sgRNA described in the present application.

[0063] On the other hand, the present application provides a method for reducing or eliminating the expression of hepatitis B virus (HBV) gene products in cells, which method includes the step of introducing the composition described in the present application into the cells, thereby reducing or eliminating the expression of the HBV gene products in the cells.

[0064] On the other hand, the present application provides a method for reducing or eliminating the expression of hepatitis B virus (HBV) gene products in a subject in vivo, the method comprising the step of introducing the composition described in the present application into the cells of the subject, thereby reducing or eliminating the expression of the HBV gene products in the subject.

[0065] On the other hand, the present application provides a method for treating a disease related to hepatitis B virus (HBV) infection in a subject or alleviating the symptoms of a disease related to HBV infection in a subject, the method comprising the step of introducing an effective amount of the composition described herein into the cells of the subject.

[0066] In certain embodiments, the subject is a mammal, such as a human, monkey, mouse, rat, rabbit, pig, horse, cat, and dog.

[0067] In certain embodiments, the method comprises administering the composition to the subject one or more times.

[0068] In certain embodiments, the method comprises administering the composition to the subject at least twice.

[0069] In certain embodiments, the interval between administering the composition more than once or at least twice is 1 day, 2 days, 3 days, 4 days, 5 days, 6 days, 7 days, 8 days, 9 days, 10 days, 11 days, 12 days, 13 days, 14 days or 15 days. For example, the method comprises administering the composition to the subject once a day, once every 2 days, once every 3 days, once every 4 days, once every 5 days, once every 6 days, once every 7 days, once every 8 days, once every 9 days, once every 10 days, once every 11 days, once every 12 days, once every 13 days, once every 14 days, or once every 15 days until the subject achieves clinical cure.

[0070] In certain embodiments, the HBV infection-related diseases include hepatitis, cirrhosis, liver fibrosis and hepatocellular carcinoma caused by HBV infection.

[0071] In certain embodiments, the composition is used to treat a disease associated with hepatitis B virus (HBV) infection in a subject or to alleviate the symptoms of a disease associated with HBV infection in a subject.

[0072] In another aspect, the present application provides a kit comprising the composition described herein and a container for placing the composition and / or instructions for use.

[0073] Those skilled in the art can easily discern other aspects and advantages of the present application from the detailed description below. In the detailed description below, only exemplary embodiments of the present application are shown and described. As will be appreciated by those skilled in the art, the content of this application enables those skilled in the art to modify the disclosed specific embodiments without departing from the spirit and scope of the invention to which this application relates. Accordingly, the descriptions in the drawings and specification of this application are merely exemplary and not restrictive. BRIEF DESCRIPTION OF THE DRAWINGS

[0074] The specific features of the inventions of this application are set forth in the appended claims. The features and advantages of the inventions of this application can be better understood by referring to the exemplary embodiments described in detail below and the accompanying drawings. A brief description of the drawings is as follows:

[0075] FIG1A is a schematic diagram of the reporter system for HBV viral protein expression described in the present application.

[0076] Figure 1B shows a schematic diagram of the screening scheme for sgRNA functional validation using the reporter cell line shown in Figure 1A.

[0077] Figures 2A-2F show the changes in fluorescence intensity after 14, 21, and 28 days of epigenetic editing of the HBV B gene using the HBx reporter cell line shown in Figure 1A. Figure 2G shows the relationship between the targeted position of the sgRNA in the HBV B genome and its knockdown ability (the ordinate is the proportion of cells knocked down by different sgRNAs 28 days after transfection, which represents the editing ability of the sgRNA; the abscissa is the position of the target sequence start site of each sgRNA in the HBV B genome).

[0078] Figures 3A-3B show the changes in fluorescence intensity 14 days after epigenetic editing of the HBV C gene using the HBx reporter cell line shown in Figure 1A. Figure 3C shows the relationship between the targeted position of the sgRNA in the HBV C genome and its knockdown ability (the ordinate is the proportion of cells knocked down by different sgRNAs 14 days after transfection, which represents the editing ability of the sgRNA; the abscissa is the position of the target sequence start site of each sgRNA in the HBV C genome).

[0079] Figures 4A-4F show the changes in fluorescence intensity 16, 21, and 28 days after epigenetic editing of the D-type HBV gene using the HBx reporter cell line shown in Figure 1A. Figure 4G shows the relationship between the targeted position of the sgRNA in the D-type HBV genome and its knockdown ability (the ordinate is the proportion of cells knocked down by different sgRNAs 28 days after transfection, which represents the editing ability of the sgRNA; the abscissa is the position of the target sequence start site of each sgRNA in the D-type HBV genome).

[0080] Figure 5A shows a schematic diagram of the method described in this application for validating epigenetic editing function in a primary hepatocyte (PHH) HBV infection model.

[0081] Figure 5B shows the antigen level results of the pharmaceutical compositions described in the present application (containing different sgRNAs) after being delivered to HBV-infected primary hepatocytes for 2 days, 4 days, 6 days, 8 days and 10 days respectively.

[0082] Figure 6 shows a schematic diagram of the process for screening sgRNA libraries in reporter cell lines.

[0083] Figure 7 shows the results of screening sgRNA libraries in three reporter cell lines for D-type HBV genes HBx, HBcAg, and HBsAg (the vertical axis is the fold change in NGS sequencing reads of different sgRNAs in the GFP-negative cell population compared with the original library 14 days after transfection, which can represent the editing ability of the sgRNA; the horizontal axis is the position of the target sequence start site of each sgRNA in the D-type HBV genome).

[0084] Figure 8 shows the effectiveness verification of candidate sgRNAs screened from the library in primary hepatocytes (PHH). The results shown are the inhibition rates of various HBV markers and PHH cell viability 14 days after HBV infection.

[0085] Figures 9A-9C show the knockdown effect of EPIREG on HBV markers in transgenic HBV mice. The results shown are the overall change curves of HBV markers in each control and treatment group, the change curves of HBV markers in each mouse in each treatment group, and the change curves of HBsAb in three mice that produced antibodies after treatment. The HBV marker levels shown in each curve were logarithmized to base 10 for data analysis.

[0086] Figure 10 shows the knockdown effect of EPIREG on HBV markers in AAV-HBV mice. The HBV marker levels shown were logarithmized to base 10 for data analysis. DETAILED DESCRIPTION

[0087] The following describes the implementation of the present invention through specific embodiments. People familiar with this technology can easily understand other advantages and effects of the present invention from the contents disclosed in this specification.

[0088] Definition of terms

[0089] In the application, the term "fusion molecule" generally refers to a molecule (bipartite molecule) consisting of at least two parts, for example, in the present application, it comprises at least one DNA binding protein described in the present application and at least one gene expression regulator described in the present application coupled to form a single entity. For example, the at least one gene expression regulator can be fused to the at least one DNA binding protein at any amino acid other than the N-terminus, C-terminus or terminal amino acid, and other molecules or parts can also be fused to the parts already contained in the fusion molecule. The parts that make up the fusion molecule can be separated by a linker or can be directly coupled. In certain embodiments, the fusion molecule is a fusion protein, which can be a chimeric protein produced by directly or indirectly covalently or non-covalently linking two or more genes, which originally encode separate proteins. In certain embodiments, translation of the fusion gene produces a single polypeptide having functional properties derived from each original protein. Those skilled in the art are fully aware of the optimal order and / or combination of determinations for determining the parts in the fusion molecule of the present application.

[0090] In this application, the terms "polynucleotide", "nucleotide", "nucleotide sequence", "nucleic acid" and "oligonucleotide" are used interchangeably. They generally refer to a polymeric form of nucleotides of any length, either deoxyribonucleotides or ribonucleotides, or analogs thereof. Polynucleotides can have any three-dimensional structure and can perform any function, known or unknown. The following are non-limiting examples of polynucleotides: coding or non-coding regions of a gene or gene fragment, multiple loci (a locus) defined by linkage analysis, exons, introns, messenger RNA (mRNA), transfer RNA, ribosomal RNA, short hairpin RNA (shRNA), micro-RNA (miRNA), ribozymes, cDNA, recombinant polynucleotides, branched polynucleotides, plasmids, vectors, isolated DNA of any sequence, isolated RNA of any sequence, nucleic acid probes, and primers. A polynucleotide may contain one or more modified nucleotides, such as methylated nucleotides and nucleotide analogs. If present, modification of the nucleotide structure can be performed before or after polymer assembly. The sequence of nucleotides can be interrupted by non-nucleotide components. A polynucleotide can be further modified after polymerization, such as by conjugation with a labeled component.

[0091] In this application, the term "DNA binding protein" generally refers to a larger protein consisting of one or more DNA binding domains (domains of different functions), which are independently folded protein domains that contain at least one motif that recognizes double-stranded or single-stranded DNA. For example, the DNA binding domain can recognize a specific DNA sequence (recognition or regulatory sequence) or has a general affinity for DNA. In some cases, other domains of the DNA binding protein typically regulate the activity of the DNA binding domain; the DNA binding function can be structural or include transcriptional regulation, and sometimes the two effects are overlapping. In certain embodiments of the methods and compositions provided herein, the DNA binding protein may include a (DNA) nuclease, such as a nuclease that can target DNA in a sequence-specific manner or can be guided or instructed to target DNA in a sequence-specific manner, such as a CRISPR-Cas system, a zinc finger nuclease (ZFN), a transcription activator-like effector nuclease (TALEN) or a large range of nucleases. In some embodiments, the DNA binding protein is a DNA nuclease derived from the CRISPR-Cas system. For example, the DNA nuclease derived from the CRISPR-Cas system is a Cas protein.

[0092] In this application, the term "Cas protein" may be used interchangeably with "CRISPR protein," "CRISPR enzyme," "CRISPR-Cas protein," "CRISPR-Cas enzyme," "Cas," "CRISPR effector," or "Cas effector protein," and is one of the components of a CRISPR-Cas system. A Cas protein (e.g., an engineered Cas protein) may have substantially the same (e.g., between 80% and 100%, between 90% and 100%, between 95% and 100%, between 98% and 100%, between 99% and 100%, between 99.9% and 100%, or about 100%) nuclease activity as a wild-type corresponding Cas protein. In some cases, an engineered Cas protein has higher (e.g., at least 5%, at least 10%, at least 20%, at least 30%, at least 40%, at least 50%, at least 60%, at least 70%, at least 80%, or at least 90%) nuclease activity than a wild-type corresponding Cas protein. Alternatively or additionally, the Cas protein (e.g., an engineered Cas protein) may have a specificity that is at least 5%, at least 10%, at least 20%, at least 30%, at least 40%, at least 50%, at least 60%, at least 70%, at least 80% or at least 90% higher than the wild-type corresponding Cas protein. In a specific example, the Cas protein (e.g., an engineered Cas protein) has a specificity that is at least 30% higher than the wild-type corresponding Cas protein. As used herein, the "specificity" of the term Cas may correspond to the number or percentage of on-target polynucleotide cleavage events relative to the number or percentage of all polynucleotide cleavage events (including on-target and off-target events). The activity and specificity of the Cas protein are consistent with those described in Hsu PD et al., DNA targeting specificity of RNA-guided Cas9 nucleases, Nat Biotechnol. 2013 Sep; 31(9): 827-832 and Slaymaker IM et al., Rationally engineered Cas9 nucleases with improved specificity, Science. 2016 Jan 1; 351(6268): 84-88, which also describe examples of methods for detecting the activity and specificity of Cas proteins and are incorporated herein by reference in their entirety.

[0093] The nucleic acid molecules encoding Cas can be codon optimized. Examples of codon-optimized sequences in this case are sequences optimized for expression in eukaryotes (e.g., humans) (i.e., optimized for expression in humans), or sequences optimized for another eukaryote such as an animal or mammal as discussed herein; see, for example, WO 2014 / 093622 (PCT / US2013 / 074667) for sequences optimized for SaCas9 humans. Although this is preferred, it should be understood that other examples are also possible, and codon optimization for host species other than humans or codon optimization for specific organs is known. In some embodiments, the enzyme coding sequence encoding Cas is codon-optimized for expression in specific cells such as eukaryotic cells. Eukaryotic cells can be cells of specific organisms (such as mammals, including but not limited to humans or non-human eukaryotes or animals or mammals as described herein, such as mice, rats, rabbits, dogs, livestock or non-human mammals or primates) or cells derived from specific organisms. In some embodiments, methods for changing human germline genetic characteristics and / or methods for changing animal genetic characteristics (described methods may cause them to suffer without any substantial medical benefit to humans or animals), as well as animals produced by such methods, can be excluded. Generally speaking, codon optimization refers to the process of modifying a nucleic acid sequence to enhance expression in a target host cell by replacing at least one codon of a native sequence with a codon that is more frequently or most frequently used in the genes of the host cell, while maintaining the native amino acid sequence. Different species show specific biases for the specific codons of specific amino acids. Codon bias (the difference in codon usage between organisms) is generally related to the translation efficiency of messenger RNA (mRNA), which is considered to depend, among other things, on the properties of the codons translated and the availability of specific transfer RNA (tRNA) molecules. The dominance of selected tRNA in cells generally reflects the most commonly used codons in peptide synthesis. Thus, genes can be tailored for optimal gene expression in a given organism based on codon optimization. Codon usage tables are readily available, for example, in the "Codon Usage Database" available at www.kazusa.orjp / codon / , and these tables can be modified in a variety of ways. See Nakamura, Y. et al. "Codon usage tabulated from the international DNA sequence databases: status for the year 2000" Nucl. Acids Res. 28:292 (2000).Computer algorithms for codon optimization of specific sequences for expression in specific host cells are also available, such as Gene Forge (Appagen; Jacobus, PA). In some embodiments, one or more codons (e.g., 1, 2, 3, 4, 5, 10, 15, 20, 25, 50 or more, or all codons) in the sequence encoding Cas correspond to the most frequently used codons for a specific amino acid.

[0094] In some embodiments, the Cas protein may have nucleic acid cleavage activity. The Cas protein may have RNA binding and DNA cleavage functions. In some embodiments, Cas can guide the location of the target sequence or its vicinity, such as within the target sequence and / or within the complementary sequence of the target sequence or at a sequence related to the target sequence, for example, about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 25, 50, 100, 200, 500 or more base pairs from the first or last nucleotide of the target sequence. In some embodiments, the Cas protein can direct more than one cleavage (e.g., one, two, three, four, five, or more cleavages) of one or both chains within the target sequence and / or within the complement of the target sequence or at a sequence related to the target sequence and / or within about 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 20, 25, 50, 100, 200, 500, or more base pairs of the first or last nucleotide of the target sequence. In some embodiments, the cleavage can be blunt-ended, i.e., produce blunt ends. In some embodiments, the cleavage can be staggered, i.e., produce sticky ends.

[0095] In some embodiments, the vector encodes a nucleic acid-targeting Cas protein, which can be mutated relative to the corresponding wild-type enzyme such that the mutated nucleic acid-targeting Cas protein lacks the ability to cleave one or both strands of a target polynucleotide containing a target sequence, for example, an alteration or mutation in the HNH domain produces a mutated Cas that substantially lacks all DNA cleavage activity, for example, the DNA cleavage activity of the mutated enzyme is about no more than 25%, 10%, 5%, 1%, 0.1%, 0.01% or less of the nucleic acid cleavage activity of the non-mutated form of the enzyme; an example is when the nucleic acid cleavage activity of the mutated form is zero or negligible compared to the non-mutated form.

[0096] In some embodiments, Cas proteins can form components of inducible systems. The inducible nature of the system will allow spatiotemporal control of gene editing or gene expression using a form of energy. The form of energy may include, but is not limited to, electromagnetic radiation, acoustic energy, chemical energy, and thermal energy. Examples of inducible systems include tetracycline-inducible promoters (Tet-On or Tet-Off), small molecule dual-hybrid transcriptional activation systems (FKBP, ABA, etc.), or light-inducible systems (phytochromes, LOV domains, or cryptochromes). In one embodiment, the CRISPR effector protein can be part of a light-inducible transcriptional effector (LITE), guiding changes in transcriptional activity in a sequence-specific manner. The components of light may include CRISPR effector proteins, light-responsive cytochrome heterodimers (e.g., from Arabidopsis thaliana), and transcriptional activation / repression domains. Other examples of inducible DNA binding proteins and methods of use thereof are provided in US 61 / 736465 and US 61 / 721,283 and WO 2014018423 A2 (which are hereby incorporated by reference in their entirety).

[0097] In some embodiments, the mutant Cas may have one or more mutations that result in reduced off-target effects, for example, for achieving modification of the target locus but reducing or eliminating off-target activity (such as when complexed with a guide RNA), and for enhancing CRISPR enzyme activity (such as when complexed with a guide RNA). It should be understood that the mutant enzymes described below can be used in any of the methods according to the present application as described elsewhere herein. Any of the methods, products, compositions and uses described elsewhere herein are also applicable to mutant CRISPR enzymes as further described below.

[0098] Can be used in various combinations to enhance or reduce the activity and / or specificity of on-target activity versus off-target activity, or to enhance or reduce the binding and / or specificity of on-target binding versus off-target binding, and can be used to compensate for or enhance the mutation or modification performed to promote other effects. Such mutations or modifications performed to promote other effects include mutations or modifications to Cas and / or mutations or modifications performed to guide RNA. The methods and mutations of the present application are used to regulate Cas nuclease activity and / or binding to chemically modified guide RNA.

[0099] In certain embodiments, the catalytic activity of the Cas protein of the present application is changed or modified. It should be understood that if the catalytic activity is different from the catalytic activity of the corresponding wild-type Cas protein (e.g., unmutated Cas protein), the mutated Cas has a changed or modified catalytic activity. The catalytic activity can be determined by methods known in the art. For example, but not limited to, by measuring the insertion / deletion (indel) percentage (e.g., after a given time, or at a given dose), the catalytic activity can be measured in vitro or in vivo. In certain embodiments, the catalytic activity is enhanced. In certain embodiments, the catalytic activity is enhanced by at least 5%, 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% or at least 100%. In certain embodiments, the catalytic activity is reduced. In certain embodiments, the catalytic activity is reduced by at least 5%, preferably at least 10%, more preferably at least 20%, such as at least 30%, at least 40%, at least 50%, at least 60%, at least 70%, at least 80%, at least 90%, or (substantially) 100%. One or more mutations herein may inactivate the catalytic activity, which may significantly reduce all catalytic activity, reduce the activity to below detectable levels, or reduce it to no measurable catalytic activity.

[0100] One or more features of the engineered Cas protein may be different from the corresponding wild-type Cas protein. Examples of such features include catalytic activity, gRNA binding, specificity of the Cas protein (e.g., editing to determine the specificity of the target), stability of the Cas protein, off-target binding, target binding, protease activity, nickase activity, and PFS recognition. In some examples, the engineered Cas protein may comprise one or more mutations of the corresponding wild-type Cas protein. In some embodiments, the catalytic activity of the engineered Cas protein is enhanced compared to the corresponding wild-type Cas protein. In some embodiments, the catalytic activity of the engineered Cas protein is reduced compared to the corresponding wild-type Cas protein. In some embodiments, the gRNA binding of the engineered Cas protein is increased compared to the corresponding wild-type Cas protein. In some embodiments, the gRNA binding of the engineered Cas protein is reduced compared to the corresponding wild-type Cas protein. In some embodiments, the specificity of the Cas protein is enhanced compared to the corresponding wild-type Cas protein. In some embodiments, the specificity of the Cas protein is reduced compared to the corresponding wild-type Cas protein. In some embodiments, the stability of the Cas protein is enhanced compared to the corresponding wild-type Cas protein. In some embodiments, the stability of the Cas protein is reduced compared to the corresponding wild-type Cas protein. In some embodiments, the engineered Cas protein further comprises one or more mutations that inactivate catalytic activity. In some embodiments, the off-target binding of the Cas protein is increased compared to the corresponding wild-type Cas protein. In some embodiments, the off-target binding of the Cas protein is reduced compared to the corresponding wild-type Cas protein. In some embodiments, the target binding of the Cas protein is increased compared to the corresponding wild-type Cas protein. In some embodiments, the target binding of the Cas protein is reduced compared to the corresponding wild-type Cas protein. In some embodiments, the engineered Cas protein has higher protease activity or polynucleotide binding ability compared to the corresponding wild-type Cas protein. In some embodiments, PFS recognition is changed compared to the corresponding wild-type Cas protein.

[0101] Examples of Cas proteins include Class I (e.g., Type I, Type III, and Type IV) and Class II (e.g., Type II, Type V, and Type VI) Cas proteins, e.g., Cas9, Cas12 (e.g., Cas12a, Cas12b, Cas12c, Cas12d), Cas13 (e.g., Cas13a, Cas13b, Cas13c, Cas13d), CasX, CasY, Cas14, variants thereof (e.g., mutant forms, truncated forms), homologs thereof, and orthologs thereof. The terms "orthologs" and "homologs" are well known in the art. By further guidance, a "homolog" of a protein as used herein is a protein of the same species that performs the same or similar function as a protein of its homolog. Homologous proteins can be, but need not be, structurally related, or only partially structurally related. A "homolog" of a protein as used herein is a protein of different species that performs the same or similar function as a protein of its ortholog. Orthologous proteins may, but need not, be structurally related, or only partially structurally related.

[0102] In some embodiments, the Cas protein is a Class 2 Cas protein, i.e., a Class 2 CRISPR-Cas system Cas protein. Class 2 CRISPR-Cas systems may have subtypes, such as type II-A, type II-B, type II-C, type VA, type VB, type VC, or type VU. In some embodiments, the Cas protein is Cas9, Cas12a, Cas12b, Cas12c, or Cas12d. In some embodiments, Cas9 may be SpCas9, SaCas9, StCas9, and other Cas9 orthologs. Cas12 may be Cas12a, Cas12b, and Cas12c, including FnCas12a or its homologs or orthologs. Definitions and exemplary members of CRISPR-Cas systems include those described in Kira S. Makarova and Eugene V. Koonin, Annotation and Classification of CRISPR-Cas systems, Methods Mol Biol. 2015; 1311: 47-75 and Sergey Shmakov et al., Diversity and evolution of class 2 CRISPR-Cas systems, Nat Rev Microbial. 2017 Mar; 15(3): 169-182.

[0103] In some instances, the Cas protein includes at least one RuvC domain and at least one HNH domain. The Cas protein may also include the first and second linker domains connecting the RuvC domain and the HNH domain. In Nishimasu, H. et al. "Crystal structure of Cas9 in complex with guide RNA and target RNA" Cell 156 (February 27, 2014, 2014): 935-949 and Ribeiro, L. et al. (2018) "Protein engineering strategies to expand CRISPR-Cas9 applications" International Journal of Genomics Volume 2018, Article ID 1652567 (doi.org / 10.1155 / 2018 / 1652567) studies, the first linker (L1) and the second linker (L2) connecting the HNH and RuvC domains in Cas9 are described. Figure 1 of Ribeiro shows the overall organization, structure and function of Cas9, which is incorporated herein by reference in particular. Specifically, Figure 1A shows a schematic diagram of the domain organization of SpCas9, showing the genetic structure of the HNH and RuvC domains including the linkers L1 (spanning amino acids 765-780) and L2 (spanning amino acids 906-918) as described herein. Similarly, when referring to the first and second linker domains, the domain organization of Staphylococcus aureus Cas9 (SaCas9) can be utilized. On the one hand, the linker 1 domain region spans residues 481-519 and connects the RuvC-II domain to the HNH domain in SaCas9. In some embodiments, the linker 2 region spans residues 629-649 and connects the RuvC-III domain of SaCas9 to the HNH domain. Therefore, the first and / or second linker domains can be mutated in Cas9 orthologs, and reference can be made to the amino acid residues corresponding to the amino acids of wild-type SaCas9. See, Nishimasu, Cell. 2015 Aug 27; 162(5): 1113-1126; doi: 10.1016 / j.cell.2015.08.007, incorporated herein by reference. In particular, Figures 1, S1-S3 of Nishimasu describe in detail the domain organization of the Cas9 protein, the teachings of which are specifically incorporated herein by reference.The first and second linkers may comprise about 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45 or more amino acids. The first and second linkers may correspond to wild-type linkers. In some aspects, the first and second linkers may comprise one or more mutations in the first and / or second linkers. On the one hand, the first and / or second linkers comprise one or more mutations that increase the specificity of the Cas9 protein. In some embodiments, the linkers L1 and L2 connecting the HNH of Cas9 to the RuvC domain contain wild-type amino acid sequences. In some embodiments, the linker connecting the HNH and RuvC domains contains a mutation in one or more amino acids. In embodiments, the first linker (L1) comprises a mutation corresponding to the amino acid T769I of SpCas9, and / or the second linker (L2) comprises a mutation corresponding to the amino acid G915M of SpCas9. In embodiments, one or more linker mutations, such as T769I and G915M, confer improved specificity to the Cas9 protein. In one embodiment, as described herein, one or more mutations in the first and second linkers can be combined with one or more mutations in other parts of the Cas9 protein to further improve specificity and / or maintain activity substantially equivalent to that of the wild-type Cas9 protein. In one embodiment, the method described in detail herein can be used to identify mutations in the linker and / or additional mutations in the Cas protein, which enhances / improves the specificity to the wild-type Cas9 and substantially retains its wild-type activity.

[0104] In some embodiments, the Cas protein can be a Cas protein (Type II Cas protein) of a Class II CRISPR-Cas system. In some embodiments, the Cas protein can be a Class II Cas protein, such as Cas9. In some embodiments, the system based on CRISPR / Cas9 may include a Cas9 protein or a fragment thereof, a Cas9 fusion protein, a nucleic acid encoding a Cas9 protein or a fragment thereof, or a nucleic acid encoding a Cas9 fusion protein. "Cas9 (CRISPR-associated protein 9)" refers to a polypeptide or fragment thereof having at least about 85% amino acid identity to NCBI accession number NP_269215 and having RNA binding activity, DNA binding activity and / or DNA cleavage activity (e.g., endonuclease or nickase activity). The function of Cas9 can be defined by any one of a variety of assays, including but not limited to a nucleic acid binding assay based on fluorescence polarization, a chain invasion assay based on fluorescence polarization, a transcription assay, an EGFP destruction assay, a DNA cleavage assay, and / or a Surveyor assay. "Cas9 nucleic acid molecule" refers to a polynucleotide encoding a Cas 9 polypeptide or a fragment thereof. An exemplary Cas9 nucleic acid molecule sequence is provided under genomic sequence number NC_002737. In some embodiments, disclosed herein are inhibitors of Cas9, such as Cas9 naturally occurring in Streptococcus pyogenes (SpCas9) or Staphylococcus aureus (SaCas9), or variants thereof. Cas9 utilizes base pairing of the protospacer adjacent motif (PAM) sequence and guide RNA (gRNA) to target DNA to identify exogenous DNA. The relative ease with which Cas9 induces targeted chain breaks at any genomic locus makes it possible to perform efficient genome editing in a variety of cell types and organisms. Cas9 derivatives can also be used as transcriptional activators / repressors.

[0105] In some cases, CRISPR-Cas protein is Cas9 or its variant. In some instances, Cas9 can be wild-type Cas9 including any naturally occurring bacterial Cas9, can be codon-optimized or modified form, including any chimera, mutant, homolog or ortholog. In another aspect of the present application, the Cas9 enzyme may include one or more mutations and can be used as a universal DNA binding protein fused to or not fused with a functional domain. The mutation can be an artificially introduced mutation or a gain-of-function or loss-of-function mutation. Other aspects of the present application relate to the Cas9 enzyme of the mutation fused to the domain, the domain including but not limited to nucleases, transcription activators, transcription repressors, recombinases, transposases, histone remodelers, demethylases, DNA methyltransferases, cryptochromes, light-inducible / controllable domains or chemically inducible / controllable domains. In some cases, the Cas9 enzyme can be from or derived from SpCas9 (Streptococcus pyogenes Cas9), saCas9 (Staphylococcus aureus Cas9) or StCas9 (wild-type Cas9 of Streptococcus thermophilus). As used herein, the term "derived" about enzyme means that the enzyme derived is based on the meaning of having a high degree of sequence homology with the wild-type enzyme to a great extent, but has been mutated (modified) in some ways known in the art or as described herein. In an example, sudden change can include one or more sudden changes in the first joint domain, the second joint domain and / or other parts of protein. Relative to wild-type enzyme, high degree of sequence homology can include at least 80%, 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or higher.

[0106] In certain embodiments, the CRISPR enzyme may be a Cas9 protein from or derived from an organism of the genera Streptococcus, Campylobacter, Nitratifractor, Staphylococcus, Parvibaculum, Roseburia, Neisseria, Gluconacetobacter, Azospirillum, Sphaerochaeta, Lactobacillus, Lactobacillus, Eubacterium, Corynebacte, Carnobacterium, Rhodobacter, Listeria, Paludibacter, Clostridium, Lachnospiraceae, Clostridiaridium, Leptotrichia, Francisella, Legionella, Alicyclobacillus yclobacillus), Methanomethyophilus, Porphyromonas, Prevotella, Bacteroidetes, Helcococcus, Letospira, Desulfovibrio, Desulfonatronum, Opitutaceae, Tuberibacillus, Bacillus, Brevibacillus bacilus), Methylobacterium or Acidaminococcus, Streptococcus, Campylobacter, Nitrobacter, Staphylococcus, Parvibaculum, Roseburia, Neisseria, Gluconacetobacter, Azospirillum, Lepidococcus, Lactobacillus, Enterobacter, Corynebacterium, Sutterella, Legionella, Treponema, Filifactor, Enterobacter, Streptococcus, Lactobacillus, Mycoplasma, Bacteroides,Flaviivola, Flavobacterium, Lepidococcus, Azospirillum, Gluconacetobacter, Neisseria, Roseburia, Parvibacter, Staphylococcus, Nitrobacter, Mycoplasma, or Campylobacter.

[0107] In some embodiments, the CRISPR enzyme can be a Cas9 protein from or derived from an organism including: S. mutans, S. agalactiae, S. equisimilis, S. sanguinis, S. pneumonia, Campylobacter jejuni, C. coli; N. tergarcus; S. auricularis, S. carnosus; N. meningitidis, N. gonorrhoeae, L. monocytogenes, L. ivanovii; C. botulinum, C. difficile, C. tetani, or C. sordellii, Francisella tularensis 1; tularensis 1), Francisella tularensis subsp. novicida, Prevotella albensis, Lachnospiraceae bacterium MC2017 1, Butyrivibrio proteoclasticus, Peregrinibacteria bacterium GW2011 GWA2_33_10, Parcubacteria bacterium GW2011GWC2_44_17, Smithella sp. SCADC, Acidaminococcus sp.BV3L6), Lachnospiraceae bacterium MA2020, Candidatus Methanoplasma termitum, Eubacterium eligens, Moraxella bovoculi 237, Leptospira inadai, Lachnospiraceae bacterium ND2006, Porphyromonas crevioricanis 3, Prevotella disiens, and Porphyromonas macacae. In some embodiments, the Cas9 protein is from an organism derived from Streptococcus pyogenes, Staphylococcus aureus, or Streptococcus thermophilus Cas9.

[0108] In a more preferred embodiment, the Cas9 protein is derived from a bacterial species selected from Streptococcus pyogenes, Staphylococcus aureus or Streptococcus thermophilus Cas9. In certain embodiments, Cas9 is derived from a bacterial species selected from Francisella tularensis 1, Prevotella alberta, Lachnospira MC20171, Butyrivibrio proteolyticus, Allopatricoccus GW2011 GWA233JO, Ponderosa GW2011 GWC2_44_17, Smithia species SCADC, Acidaminococcus species BV3L6BV3L6, Lachnospira MA2020, Methanoplasma candidate termitans, Eubacterium fastidiosa, Bovokulimora 237237, Leptospira oryzae, Spirochaete ND2006, Porphyromonas brassicae 3, Prevotella saccharolyticus and Porphyromonas macaques. In certain embodiments, the Cas9 protein is derived from a bacterial species selected from Acidaminococcus species BV3L6, Lachnospira MA2020. In certain embodiments, the effector protein is derived from a subspecies of Francisella tularensis 1, including but not limited to Francisella tularensis novyi.

[0109] Cas9 proteins include, but are not limited to, Streptococcus pyogenes serotype M1 (UniProt ID: Q99ZW2), Staphylococcus aureus Cas9 (UniProt ID: J7RUA5), Eubacterium ventriosum Cas9 (UniProt ID: A5Z395), Azospirillum (strain B510) Cas9 (UniProt ID: D3NT09), Gluconacetobacter diazophila (strain ATCC 49037) Cas9 (UnitProt ID: A9HKP2), Neisseria griseus Cas9 (UniProt ID: D0W2Z9), Roseberyella intestinalis Cas9 (UniProt ID: C7G697), Parvibacterium vegetative (strain DS-1) Cas9 (UniProt ID: A7HP89), Nitrate-lysing Bacterium nitrificans (strain DSM 16511) Cas9 (UniProt ID: D3NT09), ID:E6WZS9), Campylobacter gullus Cas9 (UniProt ID:G1UFN3).

[0110] The enzymatic action of Cas9 derived from Streptococcus pyogenes or any closely related Cas9 produces a double-strand break at a target site sequence that hybridizes to 20 nucleotides of the guide sequence and has a protospacer adjacent motif (PAM) sequence (examples include NGG / NRG, which can be determined as described herein) following the 20 nucleotides of the target sequence. The CRISPR activity of site-specific DNA recognition and cleavage by Cas9 is defined by the guide sequence, the tracr sequence that partially hybridizes to the guide sequence, and the PAM sequence. Further aspects of the CRISPR system are described in Karginov and Hannon, The CRISPR system: small RNA-guided defense in bacteria and archaea, Mole Cell 2010 Jan 15; 37(1): 7. Type II CRISPR locus from Streptococcus pyogenes SF370, which includes a cluster of four genes Cas9, Cas1, Cas2 and Csn1, and a characteristic array of two non-coding RNA elements tracrRNA and a repetitive sequence (forward repeat sequence), which is separated by a short segment (spacer, each about 30bp) of a non-repetitive sequence. In this system, targeted DNA double-strand breaks (DSBs) are produced in four consecutive steps. First, two non-coding RNAs (pre-crRNA array and tracrRNA) are transcribed from the CRISPR locus. Second, tracrRNA hybridizes with the forward repeat sequence of the pre-crRNA and is then processed into a mature crRNA containing a single spacer sequence. Third, mature crRNA: tracRNA complex is formed by a heteroduplex between the spacer of crRNA and the pre-spacer DNA, directing Cas9 to a DNA target consisting of a pre-spacer sequence and a corresponding PAM. Finally, Cas9 mediates the cutting of the target DNA upstream of PAM to produce DSBs in the protospacer. In certain embodiments, Cas9 can be constitutively present or inducibly present or conditionally present or administered or delivered. Optimization of Cas9 can be used to enhance function or develop new functions. Chimeric Cas9 proteins can be produced and Cas9 can be used as a universal DNA binding protein. The structural information provided for Cas9 can be used to further engineer and optimize the CRISPR-Cas system, and this can also infer structure-function relationships in other CRISPR enzyme systems, particularly other type II CRISPR enzymes or Cas9 orthologs. In addition, the Cas9 protein contains an easily identifiable C-terminal region that is homologous to the transposon ORF-B and includes an active RuvC-like nuclease (an arginine-rich region).

[0111] In the present application, the term "gene expression regulator" can generally be selected from a repressor of gene expression (e.g., KRAB), an activator of gene expression or a regulator of epigenetic modification (e.g., DNMT3A, DNMT3L, DNMT3A-DNMT3L fusion peptide) or any combination thereof. Different gene expression regulators are known in the art, see, for example, Thakore et al., Nat Methods.2016; 13: 127-37, incorporated herein by reference in its entirety.

[0112] In some embodiments, the gene expression regulator comprises a repressor of gene expression. The repressor can be any known repressor of gene expression, for example, can be selected from Krüppel-associated box (KRAB) domain, mSin3 interaction domain (SID), MAX-interacting protein 1 (MXI1), chromo shadow domain, ear repressor domain (SRDX), eukaryotic release factor 1 (ERF1), eukaryotic release factor 3 (ERF3), tetracycline repressor, lad repressor, Catharanthus roseus G-box binding factors 1 and 2, Drosophila Groucho, tripartite motif 28 (TRTM28), nuclear receptor corepressor 1, nuclear receptor corepressor 2, or a fragment or fusion thereof. For example, the Krüppel-associated box (KRAB) domain is a type of transcriptional repressor domain present in the N-terminal portion of many zinc finger protein-based transcription factors. The KRAB domain acts as a transcriptional repressor when linked to the target DNA through the DNA binding domain. The KRAB domain is rich in charged amino acids and can be divided into subdomains A and B. The KRAB A and B subdomains can be separated by variable spacer segments, and many KRAB proteins contain only the A subdomain. The 45-amino acid sequence in the KRAB A subdomain has been shown to be important for transcriptional repression. The B subdomain itself does not inhibit transcription, but it strengthens the inhibitory effect exerted by the KRAB A subdomain. The KRAB domain recruits the corepressor KAP1 (KRAB-associated protein-1, also known as transcription intermediary factor 1β (transcription intermediary factor 1beta), KRAB-A interacting protein and tripartite motif protein 28) and heterochromatin protein 1 (HP1), as well as other chromatin regulatory proteins, leading to transcriptional repression through heterochromatin formation. In some embodiments, the methods and compositions provided herein include a fusion molecule comprising dCas9 fused to a KRAB domain or a fragment thereof. In some embodiments, the KRAB domain or a fragment thereof is fused to the N-terminus of dCas9. In some embodiments, the KRAB domain or a fragment thereof is fused to the C-terminus of dCas9. In one embodiment, the KRAB domain or a fragment thereof is fused to both the N-terminus and the C-terminus of the dCas9 molecule.In some embodiments, the fusion molecule comprises a KRAB domain comprising the sequence set forth in SEQ ID NO: 1168, a sequence substantially identical (e.g., at least 80%, 85%, 90%, 92%, 95%, 97%, 98%, 99% or more identical) to SEQ ID NO: 1168, or a sequence having 1, 2, 3, 4, 5 or more alterations (e.g., amino acid substitutions, insertions or deletions) relative to SEQ ID NO: 1160, or any fragment thereof. In some embodiments, the zinc finger protein-based transcription factor is a KRAB domain found in many Krüppel-type C2H2 zinc finger proteins, for example, a KRAB domain derived from ZIM3 (ZIM3KRAB). For example, the fusion molecule comprises a ZIM3 KRAB domain comprising the sequence set forth in SEQ ID NO: 1196, a sequence substantially identical to SEQ ID NO: 1196 (e.g., at least 80%, 85%, 90%, 92%, 95%, 97%, 98%, 99% or higher identity), or a sequence having 1, 2, 3, 4, 5 or more alterations (e.g., amino acid substitutions, insertions or deletions) relative to SEQ ID NO: 1196, or any fragment thereof. Active fragments of other KRAB domains can be identified by any suitable alignment method known in the art.

[0113] In some embodiments, gene expression regulators include activators of gene expression. The activator can be any known gene expression activator, for example, VP16 activation domain, VP64 activation domain, p65 activation domain, Epstein-Barr (Epstein-Barr) virus R transactivator Rta molecule or the fragment described above. It is known in the art that it can be used for the activation of dCas9. See, for example, Chavez et al., Nat Methods. (2016) 13: 563-67, which is incorporated herein by reference in its entirety. In some embodiments, the methods and compositions provided herein include fusion molecules comprising dCas9 fused to VP64, p65, Rta or any combination thereof. The triple activator VP64-p65-Rta (also referred to as VPR) (wherein the three transcriptional activation domains are fused using a short amino acid linker) can effectively increase target gene expression when fused to dCas9. In some embodiments, the methods and compositions provided herein include fusion molecules comprising dCas9 fused to VPR.

[0114] In some embodiments, provided herein are methods and compositions including fusion molecules, which include the dCas9 fused to a gene expression regulator, and the gene expression regulator includes an epigenetic modification regulator. In some embodiments, the fusion molecule is modified by epigenetic modification, for example, by histone acetylation or methylation or DNA methylation, and the expression of the target gene is regulated at the regulatory element (such as promoter, enhancer or transcription start site) of the target gene. The regulator can be any known epigenetic modification regulator, for example, histone acetyltransferase (for example, p300 catalytic domain), histone deacetylase, histone methyltransferase (for example, SUV39H1 or G9a (EHMT2)), histone demethylase (for example, LSD1), DNA methyltransferase (for example, DNMT3A or DNMT3A-DNMT3L), DNA demethylase (for example, TET1 catalytic domain or TDG) or the above-described fragment.

[0115] In certain embodiments, the epigenetic modification regulator can have histone modification activity; Histone modification activity can include but is not limited to histone deacetylase, histone acetyltransferase, histone demethylase or histone methyltransferase activity. For example, the epigenetic modification regulator can have histone acetyltransferase activity, and the histone acetyltransferase can be p300 or CREB binding protein (CBP) protein or its fragment. In some embodiments, provided herein are methods and compositions including fusion molecules, which include the dCas9 fused with acetyltransferase p300 or its fragment (for example, the catalytic core of p300). In some embodiments, provided herein are methods and compositions including fusion molecules, which include the dCas9 fused with CREB binding protein (CBP) protein or its fragment. For another example, the epigenetic modification regulator can have histone demethylase activity. In some embodiments, the epigenetic modification regulator can include an enzyme that removes methyl (CH3-) groups from nucleic acid or protein (for example, histone). In some embodiments, the methods and compositions provided herein include a fusion molecule comprising a dCas9 fused to Lys-specific histone demethylase 1 (LSD1) or a fragment thereof. For another example, the epigenetic modification regulator may have histone methyltransferase activity. In some embodiments, the methods and compositions provided herein include a fusion molecule comprising a dCas9 fused to SUV39H1 or a fragment thereof. In some embodiments, the methods and compositions provided herein include a fusion molecule comprising a dCas9 fused to G9a (EHMT2) or a fragment thereof.

[0116] In certain embodiments, the epigenetic modification regulator may have DNA demethylase activity. In some embodiments, the epigenetic modification regulator may convert methyl into hydroxymethylcytosine as a mechanism for demethylating DNA. In some embodiments, provided herein are methods and compositions including fusion molecules comprising dCas9 fused to 10-11 translocation methylcytosine dioxygenase 1 (TET1) or a fragment thereof. In some embodiments, provided herein are methods and compositions including fusion molecules comprising dCas9 fused to thymine DNA glycosylase (TDG) or a fragment thereof. For another example, the epigenetic modification regulator may have DNA methylase activity. In some embodiments, the epigenetic modification regulator may have methylase activity involving transfer of methyl to DNA, RNA, protein, small molecule, cytosine or adenine. In some embodiments, provided herein are methods and compositions including fusion molecules comprising dCas9 fused to DNMT3A or a fragment thereof. In some embodiments, provided herein are methods and compositions including fusion molecules comprising dCas9 fused to DNMT3L or a fragment thereof. In some embodiments, the methods and compositions provided herein include fusion molecules comprising dCas9 fused to DNMT3L and DNMT3L or a fragment thereof. In some embodiments, the methods and compositions provided herein include fusion molecules comprising dCas9 fused to a DNMT3A-DNMT3L fusion peptide. In some embodiments, the epigenetic modification regulator having DNA methylase activity is a human-derived DNMT3L comprising the amino acid sequence shown in SEQ ID NO: 1195.

[0117] In this application, the term "guide RNA (gRNA)" is used interchangeably with "guide molecule", "guide sequence" and "single guide RNA (sgRNA)", and in the case of a CRISPR-Cas system, it generally includes any polynucleotide sequence that has sufficient complementarity with the target DNA sequence to hybridize with the target DNA sequence and guide the nucleic acid targeting complex (e.g., a composition described herein) to specifically bind to the target DNA sequence. The guide RNA can form a duplex with the target DNA sequence. In some embodiments, the guide RNA is capable of forming a complex with the CRISPR-Cas protein and includes a guide sequence that has sufficient complementarity with the target DNA sequence to hybridize with the target DNA sequence and guide the complex to sequence-specific binding of the target DNA sequence. The guide molecule or guide RNA of the CRISPR-Cas protein may include a tracr-mate sequence (including a "direct repeat sequence" in the case of an endogenous CRISPR system) and a guide sequence (also referred to as a "spacer" in the case of an endogenous CRISPR system). In some embodiments, the CRISPR-Cas system or complex described herein does not include a tracr sequence and / or is independent of the presence of a tracr sequence. In certain embodiments, the guide molecule may comprise, consist essentially of, or consist of a direct repeat sequence fused or linked to a guide sequence or a spacer sequence. In general, the CRISPR-Cas system is characterized by elements that promote the formation of a CRISPR complex at the site of a target DNA sequence, wherein hybridization between the target DNA sequence and the guide sequence promotes the formation of the CRISPR complex.

[0118] In certain embodiments, the guide sequence or spacer of a guide molecule is 15 to 50 nucleotides in length. In certain embodiments, the spacer of a guide RNA is at least 15 nucleotides in length. In certain embodiments, the spacer is 15 to 17 nucleotides in length, 17 to 20 nucleotides in length, 20 to 24 nucleotides in length, 23 to 25 nucleotides in length, 24 to 27 nucleotides in length, 27 to 30 nucleotides in length, 30 to 35 nucleotides in length, or greater than 35 nucleotides in length. In some embodiments, the guide sequence is 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, 30, 31, 32, 33, 34, 35, 36, 37, 38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 51, 52, 53, 54, 55, 56, 57, 58, 59, 60, 61, 62, 63, 64, 65, 66, 67, 68, 69, 70, 71, 72, 73, 74, 75, 76, 77, 78, 79, 80, 81, 82, 83, 84, 85, 86, 87 94, 95, 96, 97, 98, 99, or 100 nucleotides.

[0119] In some embodiments, the sequence of the guide molecule (direct repeat sequence and / or spacer) is selected to reduce the degree of secondary structure in the guide molecule. In some embodiments, when optimally folded, about or less than about 75%, 50%, 40%, 30%, 25%, 20%, 15%, 10%, 5%, 1% or less nucleotides of the nucleic acid-targeting guide RNA participate in self-complementary base pairing. Optimal folding can be determined by any suitable polynucleotide folding algorithm. Some programs are based on calculating the minimum Gibbs free energy. An example of such an algorithm is mFold, as described by Zuker and Stiegler (Nucleic Acids Res 9 (1981), 133-148). Another exemplary folding algorithm is the online web server RNAfold developed by the Institute of Theoretical Chemistry at the University of Vienna, which uses a centroid structure prediction algorithm (see, e.g., AR Gruber et al., 2008, Cell 106(1):23-24 and PA Carr and GM Church, 2009, Nature Biotechnology 27(12):1151-62).

[0120] As described above, the CRISPR / Cas9 system utilizes gRNA to provide targeting of a CRISPR / Cas9-based system. gRNA is a fusion of two non-coding RNAs: crRNA and tracrRNA. By exchanging the sequence encoding the 20bp pre-spacer sequence, sgRNA can target any desired DNA sequence, and the pre-spacer sequence confers targeting specificity by complementary base pairing with the desired DNA target. gRNA mimics the naturally occurring crRNA:tracrRNA duplex involved in the type II effector system. The duplex (which may include, for example, a 42-nucleotide crRNA and a 75-nucleotide tracrRNA) serves as a guide for Cas9 to cut the target nucleic acid.

[0121] On the other hand, the sgRNA provided herein may further comprise a scaffold sequence having: a nucleotide sequence as set forth in SEQ ID NO: 1190; or a nucleotide sequence having 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%, at least 99%, at least 99.9% or at least 100% sequence identity with the nucleotide sequence as set forth in SEQ ID NO: 1190 and retaining its biological activity; or a nucleotide sequence modified based on the nucleotide sequence of SEQ ID NO: 1190 and retaining its biological activity. For example, the modification may be one or more of base phosphorylation, base sulfidation, base methylation, base hydroxylation, sequence shortening and sequence lengthening. Furthermore, the sequence shortening and sequence lengthening may comprise deletion or addition of 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 bases relative to the base sequence.

[0122] As an example only, the scaffold sequence may be:

[0123] In some embodiments, the sgRNA provided herein may further include the CRISPR spacer sequence at the 5' end of the scaffold sequence, and the CRISPR spacer sequence is a sequence having a length of 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, or 30 nucleotides and capable of complementary pairing with the target sequence. In some preferred embodiments, the CRISPR spacer sequence is a sequence having a length of 20 or 21 nucleotides and capable of complementary pairing with the target sequence. In some embodiments, the sgRNA may further include a terminator at the 3' end of the spacer sequence. For example, the terminator may be a terminator consisting of a plurality of, for example, at least 6 (e.g., 7 or 8) Us.

[0124] In the present application, the terms "target DNA" and "target sequence" or "pre-spacer sequence" are used interchangeably, and generally refer to a nucleotide sequence present in a target nucleic acid, which comprises a core base sequence complementary to the oligonucleotides (e.g., guide RNA) of the present application. In some cases, the target sequence is composed of a region complementary to the continuous nucleotide sequence of the oligonucleotides of the present application on the target nucleic acid. In some cases, the target sequence is longer than the complementary sequence of a single oligonucleotide and can, for example, represent an optional region of the target nucleic acid that can be targeted by several oligonucleotides of the present application. In some cases, "target sequence" can mean a part of a target gene, such as one or more exon sequences of a target gene, an intron sequence, or a regulatory sequence of a target gene, or a combination of exons and intron sequences, introns and regulatory sequences, exons and regulatory sequences, or exons, introns and regulatory sequences of a target gene. In the context of the formation of the CRISPR complex of the present application or the system, "target DNA" refers to a sequence that a guide RNA sequence is designed to have complementarity thereto, wherein the hybridization between the target DNA and the guide RNA sequence promotes the formation of a CRISPR complex or system. In some embodiments, the target DNA is located in the nucleus or cytoplasm of the cell. A CRISPR / Cas9-based system can include at least one gRNA, wherein the gRNAs target different DNA sequences. The target DNA sequences can be overlapping. The target sequence or pre-spacer sequence is followed by a PAM sequence located at the 3' end of the pre-spacer sequence. Different type II systems have different PAM requirements. For example, the type II Streptococcus pyogenes system uses an "NGG" sequence, where "N" can be any nucleotide.

[0125] In some embodiments, the number of gRNAs administered to the cells can be at least 1 gRNA, at least 2 different gRNAs, at least 3 different gRNAs, at least 4 different gRNAs, at least 5 different gRNAs, at least 6 different gRNAs, at least 7 different gRNAs, at least 8 different gRNAs, at least 9 different gRNAs, at least 10 different gRNAs, at least 11 different gRNAs, at least 12 different gRNAs, at least 13 different gRNAs, at least 14 different gRNAs, at least 15 different gRNAs, at least 16 different gRNAs, at least 17 different gRNAs, at least 18 different gRNAs, at least 19 different gRNAs, at least 20 different gRNAs, at least 25 different gRNAs, at least 30 different gRNAs, at least 35 different gRNAs, at least 40 different gRNAs, at least 45 different gRNAs, or at least 50 different gRNAs.

[0126] In some embodiments, the number of gRNAs administered to a cell can be from at least 1 gRNA to at least 50 different gRNAs, from at least 1 gRNA to at least 45 different gRNAs, from at least 1 gRNA to at least 40 different gRNAs, from at least 1 gRNA to at least 35 different gRNAs, from at least 1 gRNA to at least 30 different gRNAs, from at least 1 gRNA to at least 25 different gRNAs, from at least 1 gRNA to at least 20 different gRNAs, from at least 1 gRNA to at least 16 different gRNAs, from at least 1 gRNA to at least 12 different gRNAs, from at least 1 gRNA to at least 8 different gRNAs, from at least 1 gRNA to at least 4 different gRNAs, from at least 4 different gRNAs to at least 50 different gRNAs, from at least 4 different gRNAs to at least 45 different gRNAs, from at least 4 different gRNAs to at least 40 different gRNAs, from at least 4 different gRNAs to at least 35 ...0 different gRNAs, from at least 1 gRNA to at least 25 different g In some embodiments, the transcription of a target gene is increased or decreased by selecting a gRNA.

[0127] As used herein, the term "regulatory element" refers to a genetic element that can control the expression of a nucleic acid sequence. For example, splicing signals, promoter sequences, polyadenylation signals, transcription termination sequences, upstream regulatory domains, replication origins, internal ribosome entry sites ("IRES"), enhancers, etc., together provide for the replication, transcription, and translation of coding sequences in recipient cells. Not all of these control sequences need to be present. Transcriptional control signals in eukaryotes typically include "promoter" and "enhancer" elements. Promoters and enhancers are composed of short arrays of DNA sequences. Promoters are regulatory elements that promote the initiation of transcription of operably linked coding regions, while enhancers increase the activity of the closest promoter on the same DNA molecule, thereby increasing the speed of genetic transcription. These sequences specifically interact with cellular proteins involved in transcription (Maniatis et al., Science 236:1237 (1987), incorporated herein by reference in their entirety). Promoter and enhancer elements have been isolated from various eukaryotic sources, including genes in yeast, insect and mammalian cells, and viruses (similar control sequences, i.e., promoters, are also found in prokaryotes). The selection of a specific promoter and enhancer depends on the recipient cell type. Some eukaryotic promoters and enhancers have a broad host range, while others are functional in a limited subset of cell types (for review, see, e.g., Voss et al., Trends Biochem. Sci., 11: 287 (1986); and Maniatis et al. (ibid.), incorporated herein by reference in their entirety). For example, the SV40 early gene enhancer is very active in a variety of cell types from many mammalian species and has been used to express proteins in a variety of mammalian cells (Dijkema et al., EMBO J. 4: 761 (1985), incorporated herein by reference in its entirety). Promoter and enhancer elements derived from the human elongation factor 1-alpha gene (Uetsuki et al., J. Biol. Chem., 264: 5791 (1989); Kim et al., Gene 91: 217 (1990); and Mizushima and Nagata, Nucl. Acids. Res., 18: 5322 (1990)), the long terminal repeat of Rous sarcoma virus (Gorman et al., Proc. Natl. Acad. Sci. USA 79: 6777 (1982)), and human cytomegalovirus (Boshart et al., Cell 41: 521 (1985)) can also be used to express proteins in different mammalian cell types, and the references are incorporated herein by reference in their entirety. Promoters and enhancers can occur alone or together in nature. For example, retroviral long terminal repeats contain promoter and enhancer elements.In general, the effects of promoters and enhancers are independent of the genes being transcribed or translated. Thus, the enhancers and promoters used can be "endogenous," "exogenous," or "heterologous" relative to the genes to which they are operably linked. An "endogenous" enhancer / promoter is one that is naturally linked to a given gene in the genome. An "exogenous" or "heterologous" enhancer or promoter is one that is juxtaposed to a gene by genetic manipulation (i.e., molecular biology techniques) such that transcription of the gene is directed by the linked enhancer / promoter. The presence of a "splicing signal" on an expression vector typically results in high-level expression of the recombinant transcript.

[0128] In certain embodiments, a "splicing signal" mediates the removal of introns from the primary RNA transcript and consists of a splice donor and acceptor site (Sambrook et al., Molecular Cloning: A Laboratory Manual, 2nd ed., Cold Spring Harbor Laboratory Press, New York (1989), pp. 16.7-16.8, incorporated herein by reference in its entirety). A commonly used splice donor and acceptor site is the splice junction of the 16S RNA from SV40.

[0129] In certain embodiments, a "transcription termination signal" is typically present downstream of the polyadenylation signal and is hundreds of nucleotides in length. For example, the term "poly A signal" or "poly A sequence" refers to a DNA sequence that directs the termination and polyadenylation of a nascent RNA transcript. Efficient polyadenylation of recombinant transcripts is often necessary because transcripts lacking a poly A signal are unstable and rapidly degraded. The poly A signal used in an expression vector can be "heterologous" or "endogenous." An endogenous poly A signal is a signal naturally present at the 3' end of the coding region of a given gene in the genome. A heterologous poly A signal is a signal isolated from a gene and operably linked to the 3' end of another gene. A commonly used heterologous poly A signal is the SV40 poly A signal. The SV40 poly A signal is contained on a 237 bp BamHI / BclI restriction fragment and directs termination and polyadenylation (Sambrook et al., supra, 16.6-16.7, incorporated by reference in its entirety).

[0130] In this application, the term "inactivated Cas9 protein" may be referred to as "dCas9" protein. Methods for generating Cas9 proteins (or fragments thereof) with inactivated DNA cleavage domains are known, for example, Jinek et al., Science. 337: 816-821 (2012); Qi et al., "Repurposing CRISPR as an RNA-Guided Platform for Sequence-Specific Control of Gene Expression", Cell. 28, 152(5): 1173-83 (2013), the entire contents of each of which are incorporated herein by reference). For example, it is known that the DNA cleavage domain of Cas9 includes two subdomains, the HNH nuclease subdomain and the RuvC1 subdomain. The HNH subdomain cuts the strand complementary to the gRNA, while the RuvC1 subdomain cuts the non-complementary strand. Mutations in these subdomains can silence the nuclease activity of Cas9. For example, mutations D10A and H840A completely inactivate the nuclease activity of Streptococcus pyogenes Cas9 (Jinek et al., Science. 337: 816-821 (2012); Qi et al., Cell. 28; 152 (5): 1173-83 (2013)). Suitable CRISPR inactivation or nicking DNA binding domains include, but are not limited to, nuclease-inactivated variant Cas9 domains including D10A, D10A / D839A / H840A, and D10A / D839A / H840A / N863A mutant domains, as described in WO2015089406A1, which is incorporated herein by reference. In some cases, dCas9 from Streptococcus pyogenes without endonuclease activity has been targeted by gRNA to genes in bacteria, yeast, and human cells to silence gene expression by steric hindrance. As used herein, "dCas" may refer to a dCas protein or a fragment thereof. As used herein, "dCas9" may refer to a dCas9 protein or a fragment thereof. As used herein, the terms "iCas" and "dCas" are used interchangeably to refer to a CRISPR-associated protein without catalytic activity. In one embodiment, the dCas protein comprises one or more mutations in the DNA cleavage domain. In one embodiment, the dCas protein comprises one or more mutations in the RuvC or HNH domain. In one embodiment, the dCas molecule comprises one or more mutations in both the RuvC and HNH domains. In one embodiment, the dCas protein is a fragment of a wild-type Cas protein. In one embodiment, the dCas protein comprises a functional domain from a wild-type Cas protein, wherein the functional domain is selected from a Reel domain, a bridge helix domain, or a PAM interaction domain.In one embodiment, the nuclease activity of the dCas is reduced by at least 40%, 45%, 50%, 55%, 60%, 65%, 70%, 75%, 80%, 85%, 90%, 95% or 99% compared to the nuclease activity of the corresponding wild-type Cas protein.

[0131] Suitable dCas can be derived from wild-type Cas protein. Cas protein can be from type I, type II or type III CRISPR-Cas system. In one embodiment, suitable dCas can be derived from Cas1, Cas2, Cas3, Cas4, Cas5, Cas6, Cas7, Cas8, Cas9 or Cas10. In one embodiment, dCas is derived from Cas9 protein. For example, dCas9 can be obtained by introducing point mutations (e.g., substitutions, deletions or additions) in the DNA cleavage domain (e.g., nuclease domain, e.g., RuvC and / or HNH domain) of Cas9 protein. See, e.g., Jinek et al., Science (2012) 337: 816-21, incorporated herein by reference in its entirety. For example, introducing two point mutations in RuvC and HNH domains reduces Cas9 nuclease activity while retaining Cas9 sgRNA and DNA binding activity. In one embodiment, the two point mutations in RuvC and HNH active sites are D10A and H840A mutations of Streptococcus pyogenes Cas9. Alternatively, D10 and H840 of Streptococcus pyogenes Cas9 can be deleted to eliminate Cas9 nuclease activity while retaining its sgRNA and DNA binding activity. In one embodiment, the two point mutations within the RuvC and HNH active sites are the D10A and N580A mutations of Streptococcus pyogenes Cas9.

[0132] In various embodiments, the present application relates to a dCas protein or any variant or mutant thereof. All variants and mutants of dCas9 can be used in the methods, compositions, fusion molecules, or kits disclosed herein, including but not limited to those derived from SpCas9 (Cas9 isolated from Streptococcus pyogenes), SaCas9 (Cas9 isolated from Staphylococcus aureus), StCas9 (Cas9 isolated from Streptococcus thermophilus), NmCas9 (Cas9 isolated from Neisseria meningitidis), FnCas9 (Cas9 isolated from Francisella novicida), CjCas9 (Cas9 isolated from Campylobacter jejuni), ScCas9 (Cas9 isolated from Streptococcus canis), and any variant and mutant forms of Cas9 listed above, such as high-fidelity Cas9 (Kleinstiver et al., Nature. January 28, 2016) and enhanced SpCas9 (Slaymaker et al., Sciences. January 1, 2016). For example, the dCas9 sequences shown in SEQ ID NOs: 1170-1187 of the present application only provide a few exemplary options and are not exclusive. In one embodiment, the dCas protein is a Streptococcus pyogenes dCas9 protein comprising a mutation at D10 and / or H840 (as shown in SEQ ID NO: 1170). In one embodiment, the dCas protein is a Streptococcus pyogenes dCas9 protein comprising a D10A and / or H840A mutation (as shown in SEQ ID NO: 1170). In one embodiment, the dCas9 protein is a Staphylococcus aureus dCas9 protein comprising the amino acid sequence set forth in any one of SEQ ID NOs: 1171-1173, a sequence substantially identical (e.g., at least 80%, 85%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or more sequence identity) to any one of SEQ ID NOs: 1171-1173, or a sequence having 1, 2, 3, 4, 5 or more alterations (e.g., amino acid substitutions, insertions or deletions) relative to any one of SEQ ID NOs: 1171-1173, or any fragment thereof.

[0133] Similar mutations can also be applied to any other naturally occurring Cas9 (e.g., Cas9 from other species) or engineered Cas9. In certain embodiments, the dCas9 comprises Streptococcus pyogenes dCas9, Staphylococcus aureus dCas9, Campylobacter jejuni dCas9, Corynebacterium diphtheria dCas9, Eubacterium ventriosum dCas9, Streptococcus pasteurianus dCas9, Lactobacillus farciminis dCas9, Sphaerochaeta globus dCas9, Azospirillum (e.g., strain B510) dCas9, Gluconacetobacter diazotrophicus dCas9, Neisseria cinerea dCas9, Roseburia enterica dCas9, and Streptococcus pasteurianus dCas9. intestinalis) dCas9, Parvibaculum lavamentivorans) dCas9, Nitratifractor salsuginis (e.g., strain DSM 16511) dCas9, Campylobacter lari (e.g., strain CF89-12) dCas9, Streptococcus thermophilus (e.g., strain LMD-9) dCas9, or fragments thereof. In certain embodiments, the present application also provides a vector comprising a nucleotide encoding the following protein molecule: Streptococcus pyogenes dCas9, Staphylococcus aureus dCas9, Campylobacter jejuni dCas9, Corynebacterium diphtheriae dCas9, Eubacterium convexogastricum dCas9, Streptococcus pasteurianum dCas9, Lactobacillus farinae dCas9, Trichoderma sphaeroides dCas9, Azospirillum (strain B510) dCas9, Gluconacetobacter diazophila dCas9, Neisseria griseus dCas9, Roseburia intestinalis dCas9, Microbacterium edodes dCas9, Brine Nitrate Lysing Bacteria (strain DSM 16511) dCas9, Campylobacter seagulls (strain CF89-12) dCas9, Streptococcus thermophilus (strain LMD-9) dCas9 or a fragment thereof.

[0134] In this application, the term "nucleotide modification" may mean that the nucleic acids described in the present invention are synthesized or modified by methods well-established in the art, such as the methods described in "Current protocols in nucleic acid chemistry" Beaucage, SL et al. (Edrs.), John Wiley & Sons, Inc., New York, NY, USA (which is incorporated herein by reference). The modification may include, but is not limited to, terminal modifications, such as 5'-terminal modifications (e.g., phosphorylation, conjugation, inverted linkage) or 3'-terminal modifications (e.g., conjugation, DNA nucleotides, inverted linkage, etc.); base modifications, such as substitution with stabilized bases, destabilized bases, or bases that pair with an extended pairing repertoire, removal of bases (abasic nucleotides), or conjugated bases; sugar modifications (e.g., sugar modification at the 2'-position or 4'-position) or replacement of sugars; or backbone modifications, including modification or substitution of phosphodiester bonds.

[0135] In this application, the terms "DNA methylation" and "nucleic acid methylation" are used interchangeably and generally refer to the methylation state of a gene fragment, nucleotide, or base thereof in this application, a process that often occurs inside a cell that has been transfected with a nucleic acid comprising a structural gene encoding a polypeptide operably linked to a promoter, during which the cytosines of the promoter nucleic acid are converted to 5-methylcytosine. A promoter nucleic acid in which at least one cytosine is converted to 5-methylcytosine is referred to as a "methylated" nucleic acid or DNA. In this application, the DNA fragment in which the gene is located may be methylated on one or more strands, and may also be methylated at one or more sites.

[0136] In this application, the term "portion thereof" generally refers to a portion or fragment of a specified whole. For example, when used in this application relative to a specified polypeptide sequence, the term "portion thereof" refers to a continuous length of the sequence of a specified polypeptide that is shorter than the full-length sequence of the specified polypeptide. A portion of a specified polypeptide can be defined by its first position and its last position, wherein the first and last positions each correspond to a position in the sequence of the specified polypeptide, wherein the sequence position corresponding to the first position is located N-terminal to the sequence position corresponding to the last position, and whereby the sequence of the portion is a continuous amino acid sequence in the specified polypeptide that begins at the sequence position corresponding to the first position and ends at the sequence position corresponding to the last position. A portion can also be defined by reference to a position in the sequence of a specified polypeptide and the residue length relative to the reference position, whereby the sequence of the portion is a continuous amino acid sequence in the specified polypeptide that has a defined length and is positioned in the specified polypeptide according to the defined position.

[0137] In the present application, the term "direct or indirect fusion" generally refers to the relative "direct fusion" or "indirect fusion". The term "direct fusion" generally refers to direct connection or direct binding. For example, the direct connection can be a situation where there is no spacer component (such as an amino acid residue or its derivative) between the connected substances (such as amino acid sequence segments) and they are directly connected; for example, an amino acid sequence segment X is directly connected to another amino acid sequence segment Y through an amide bond formed by the C-terminal amino acid of the amino acid sequence segment X and the N-terminal amino acid of the amino acid sequence segment Y. "Indirect fusion" generally refers to a situation where there is a spacer component (such as an amino acid residue or its derivative) between the connected substances (such as amino acid sequence segments) and they are indirectly connected.

[0138] In the present application, the carrier used to package the composition, fusion molecule and / or guide molecule (sgRNA) described in the present application may include a lipid particle, for example, the lipid particle may be a lipid nanoparticle (LNP) and a liposome.

[0139] For example, as used herein, the term "lipid nanoparticle (LNP)" or "an LNP" or "multiple LNPs" generally refers to a particle comprising multiple (i.e., more than one) lipid molecules physically bound to each other (e.g., covalently or non-covalently) by intermolecular forces. LNPs can be, for example, microspheres (including unilamellar and multilamellar vesicles, such as liposomes), dispersed phases in emulsions, micelles, or internal phases in suspensions. LNPs can encapsulate nucleic acids in cationic lipid particles (e.g., liposomes) and can be delivered to cells relatively easily. In some instances, lipid nanoparticles do not contain any viral components, which helps to minimize safety and immunogenicity issues. The lipid particles can be used for in vitro, ex vivo, and in vivo delivery. The lipid particles can also be used for cell populations of various sizes. The LNPs of the present application can be easily prepared by various methods known in the art, such as by mixing an organic phase with an aqueous phase. The mixing of the two phases can be achieved by microfluidic devices and impinging stream reactors. The more fully the organic phase and the aqueous phase are mixed, the better the embedding efficiency and particle size distribution of the LNPs obtained. Preferably, the particle size of LNP can be adjusted by changing the mixing speed of the organic phase and the aqueous phase. The faster the mixing speed, the smaller the particle size of the prepared LNP will be. The embedding efficiency can be optimized by adjusting the N / P (ionizable lipid / nucleic acid) ratio of the LNP system. In some preferred embodiments, the N / P ratio is 1: 1-9: 1. In some examples, LNP can be used to deliver DNA molecules (e.g., molecules comprising coding sequences of DNA binding proteins and / or sgRNA) and / or RNA molecules (e.g., mRNA of Cas, sgRNA). In some cases, LNP can be used to deliver RNP complexes of Cas / gRNA. In some embodiments, LNP is used to deliver mRNA and gRNA (e.g., mRNA fusion molecules comprising DNMT3A-DNMT3L (3A-3L)-dCas9-KRAB or DNMT3A-DNMT3L-ZIM3 KRAB-dCas9, and at least one sgRNA targeting the HBV gene).

[0140] The components of LNP can include cationic lipids 1,2-phthalic acid-3-dimethylammonium-propane (DLinDAP), 1,2-dilinoleyloxy-3-N,N-dimethylaminopropane (DLinDMA), 1,2-dilinoleyloxyketone-N,N-dimethyl-3-aminopropane (DLinK-DMA), 1,2-dilinoleyl-4-(2-dimethylaminoethyl)-. In some embodiments, LNP can include ionizable lipids. In some embodiments, ionizable lipids include but are not limited to pH responsive ionizable lipids, thermal responsive ionizable lipids and light responsive ionizable lipids. In some embodiments, ionizable lipids include cationic lipids and anionic lipids that ionize under certain conditions (such as but not limited to pH, temperature or light). In some embodiments, the molar ratio of ionizable lipids of the LNP is from 20% to about 70% (e.g., from about 20% to about 70%, from about 20% to about 65%, from about 20% to about 60%, from about 20% to about 55%, from about 20% to about 50%, from about 20% to about 45%, from about 20% to about 40%, from about 20% to about 35%, from about 20% to about 30%, from about 20% to about 25%, from about 30% to about 70%, from about 30% to about 65%, from about 30% to about 60%, from about 30% to about 50%). In some embodiments, the LNPs may comprise PEGylated lipids. In some embodiments, the LNPs may comprise PEGylated lipids. In some embodiments, the LNPs may comprise PEGylated lipids. In some embodiments, the LNPs may comprise PEGylated lipids. In some embodiments, the LNPs may comprise PEGylated lipids. In some embodiments, the LNPs may comprise PEGylated lipids. In some embodiments, the molar ratio of the PEGylated lipid of the LNP is 0% to about 30% (e.g., about 0% to about 30%, about 0% to about 25%, about 0% to about 20%, about 0% to about 15%, about 0% to about 10%, about 10% to about 30%, about 10% to about 25%, about 10% to about 20%, about 10% to about 15%, about 20% to about 30%, or about 20% to about 25%). In some embodiments, the LNP may comprise a supporting lipid. In some embodiments, the molar ratio of the supporting lipid of the LNP is 30% to about 50% (e.g., about 30% to about 50%, about 30% to about 45%, about 30% to about 40%, about 30% to about 35%, about 40% to about 50%, or about 40% to about 45%). In some embodiments, the LNP may comprise cholesterol.In some embodiments, the molar ratio of cholesterol in the LNP is from 10% to about 50% (e.g., from about 10% to about 50%, from about 10% to about 45%, from about 10% to about 40%, from about 10% to about 35%, from about 10% to about 30%, from about 10% to about 25%, from about 10% to about 20%, from about 10% to about 15%, from about 20% to about 50%, from about 20% to about 45%, from about 20% to about 40%, from about 20% to about 35%, from about 20% to about 30%, from about 20% to about 25%, from about 30% to about 50%, from about 30% to about 45%, from about 30% to about 40%, from about 30% to about 35%, from about 40% to about 50%, or from about 40% to about 45%). In some embodiments, LNPs may comprise a mixture of ionizable lipids (20%-70%, molar ratio), PEGylated lipids (0%-30%, molar ratio), supporting lipids (30%-50%, molar ratio) and cholesterol (10%-50%, molar ratio).

[0141] For example, as used herein, the term "liposome" generally refers to a vesicle with an internal space that is isolated from an external medium by one or more bilayer membranes. In some embodiments, the bilayer membrane can be formed by amphiphilic molecules, such as synthetic or naturally derived lipids comprising spatially isolated hydrophilic and hydrophobic domains; in other embodiments, the bilayer membrane can be formed by amphiphilic polymers and surfactants. In some embodiments, the liposome is a spherical vesicle structure consisting of a monolayer or multilayer lipid bilayer surrounding an internal aqueous compartment and a relatively impermeable external lipophilic phospholipid bilayer. In some embodiments, liposomes are biocompatible, non-toxic, can deliver hydrophilic and lipophilic drug molecules, protect their cargo from being degraded by plasma enzymes, and transport their loads across biological membranes and the blood-brain barrier (BBB). Liposomes can be made of several different types of lipids such as phospholipids. Liposomes can comprise natural phospholipids and lipids such as 1,2-distearoyl-sn-glycero-3-phosphatidylcholine (DSPC), sphingomyelin, egg phosphatidylcholine, monosialoganglioside, or any combination thereof. In order to modify the structure and properties of the liposomes, several other additives can be added to the liposomes. For example, the liposomes can also comprise cholesterol, sphingomyelin, and / or 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (DOPE), for example, to increase stability and / or prevent leakage of cargo inside the liposomes.

[0142] In this application, the term "adeno-associated virus (AAV) vector" generally refers to a vector with a functional or partially functional ITR sequence and a transgene. As used herein, the term "ITR" refers to an inverted terminal repeat sequence. The ITR sequence can be derived from an adeno-associated virus serotype, including but not limited to AAV-1, AAV-2, AAV-3, AAV-4, AAV-5, AAV-6, AAV7, AAV8, AAV9, AAV10, AAV11, AAV12 and AAV13, and any AAV variant or mixture. However, ITR does not have to be a wild-type nucleotide sequence and can be changed (e.g., by insertion, deletion or substitution of nucleotides) as long as the sequence retains the function of providing functional rescue, replication and packaging. The AAV vector may have one or more fully or partially deleted AAV wild-type genes, preferably rep and / or cap genes, but retains functional flanking ITR sequences. Functional ITR sequences play a role in, for example, rescuing, replicating and packaging AAV virus particles or particles. Thus, an "AAV vector" is defined herein as comprising at least those sequences required for insertion of a transgene into a subject's cells, and optionally comprising those cis sequences necessary for viral replication and packaging (e.g., functional ITRs).

[0143] In this application, the term "pharmaceutically acceptable carrier" generally refers to a carrier for administering therapeutic agents, such as antibodies or polypeptides, genes, and other therapeutic agents. The term refers to any pharmaceutical carrier that does not itself induce the production of antibodies harmful to the individual receiving the composition and that can be administered without excessive toxicity. Suitable carriers can be large, slowly metabolized macromolecules, such as proteins, polysaccharides, polylactic acids, polyglycolic acids, polyamino acids, amino acid copolymers, lipid aggregates, and inactivated viral particles. These carriers are well known to those skilled in the art. Pharmaceutically acceptable carriers in therapeutic compositions can include liquids such as water, saline, glycerol, and ethanol. Auxiliary substances, such as wetting agents or emulsifiers, pH buffering substances, etc., may also be present in these carriers.

[0144] In this application, the term "sequence encoding..." or "nucleic acid encoding..." generally refers to a nucleic acid (RNA or DNA molecule) comprising a nucleotide sequence encoding a protein. The coding sequence may also include start and stop signals operably linked to regulatory elements, including a promoter and a polyadenylation signal capable of directing expression in the cells of an individual or mammal to which the nucleic acid is administered. The coding sequence may be codon-optimized. In some embodiments, the coding nucleic acid may be mRNA; one or more modification techniques may be used to produce more stable mRNA. Known mRNA modification techniques can be broadly divided into three categories: synthesizing mRNA using artificially synthesized non-natural RNAs instead of natural RNAs; adding 5' caps, 3' poly(A) "tails," and UTR (untranslated region) sequences; and employing specialized novel formulation techniques to effectively protect mRNA. Among these, a preferred mRNA modification technique involves synthesizing mRNA using artificially synthesized non-natural RNAs instead of natural RNAs. Chemical modifications on eukaryotic mRNA can be broadly divided into three categories: methylation, pseudouridine (Ψ), and hypoxanthine. For example, the chemical modification can be selected from the group consisting of pseudouridine, N1-methylpseudouridine, N1-ethylpseudouridine, 2-thiouridine, 4'-thiouridine, 5-methylcytosine, 2-thiol-1-methyl-1-deaza-pseudouridine, 2-thiol-1-methyl-pseudouridine, 2-thiol-5-aza-uridine, 2-thiol-dihydropseudouridine, 2-thiol-dihydrouridine, 2-thiol-pseudouridine, 4-methoxy-2-thiol-pseudouridine, 4-methoxy-pseudouridine, 4-thiol-1-methyl-pseudouridine, 4-thiol-pseudouridine, 5-aza-uridine, dihydropseudouridine, 5-methyluridine, 5-methoxyuridine and 2'-O-methyluridine.

[0145] In this application, the term "complementary" generally refers to the Walson-Crick (e.g., AT / U and CG) or Hoogsteen base pairing between nucleotides or nucleotide analogs of a nucleic acid molecule. "Complementarity" refers to the property shared by two nucleic acid sequences such that when they are arranged antiparallel to each other, the nucleotide bases at every position will be complementary.

[0146] In this application, the terms "subject" and "patient" are used interchangeably and generally refer to humans and non-human animals. The term "non-human animal" as used herein includes all vertebrates, e.g., mammals and non-mammals, such as non-human primates, sheep, dogs, cats, horses, cows, chickens, amphibians, reptiles, etc.

[0147] In this application, the terms "effective amount" and "therapeutically effective amount" or "therapeutically effective dose" are used interchangeably and generally refer to an amount or dose of a fusion molecule (protein), polypeptide, nucleic acid, lipid nanoparticle, liposome, one or more AAV particles or one or more virions that can produce sufficient amounts of the desired protein to modulate protein activity in the desired manner, thereby providing a relief tool for clinical intervention. In certain embodiments, a therapeutically effective amount or dose of a transfected fusion protein, polypeptide, nucleic acid, one or more AAV particles or one or more virions as described herein is sufficient to confer inhibition of the gene targeted by the fusion protein / gene therapy construct.

[0148] As used herein, the term "treating," e.g., treating, a disease, means that a subject (e.g., a human) having the disease, at risk of having the disease, and / or experiencing symptoms of the disease will, in one embodiment, experience less severe symptoms and / or will recover more quickly when administered, e.g., a fusion molecule or a nucleic acid encoding the fusion molecule and / or a gRNA or a nucleic acid encoding the gRNA as described herein, compared to when the fusion molecule or a nucleic acid encoding the fusion molecule and / or the gRNA or a nucleic acid encoding the gRNA has never been administered.

[0149] Without intending to be bound by any theory, the following examples are merely intended to illustrate the compositions, methods of use and applications of the present application, and are not intended to limit the scope of the present invention.

[0150] Example

[0151] Example 1

[0152] Construction and functional screening of sgRNA libraries targeting the hepatitis B virus (HBV) gene

[0153] (1) Construction of sgRNA libraries for HBV B, C, and D genes

[0154] This example uses the genome sequence of hepatitis B virus (HBV), which includes the complete genome of polynucleotides encoding HBV polymerase Pol, surface antigen HBsAg, HBV X protein, and core region antigen precursor HBcAg. These genomes are divided into HBV type B (serotype adw subtype), HBV type C (serotype adr subtype), and HBV type D (serotype ayw subtype), as shown in the following table.

[0155] (2) sgRNA functional screening

[0156] 293FT was used to construct reporter cell lines targeting HBV surface antigen (HBsAg), core antigen (HBcAg), X protein (HBx), and polymerase (Pol) for genotypes B, C, and D. A schematic diagram is shown in Figure 1A. The genomic sequence containing the CpG island and regulatory elements preceding the protein transcription start site was retained. The gene sequences for the self-cleaving peptide P2A and EGFP were fused after amino acid 38 of the HBV surface antigen (HBsAg), amino acid 129 of the core antigen (HBcAg), amino acid 77 of the X protein (HBx), and amino acid 177 of the polymerase (Pol), respectively. The reporter genes were integrated into the 293FT genome using the PiggyBac transposon system, and stably transfected cell lines were constructed. Fluorescence intensity was used to reflect protein expression levels, allowing for rapid functional validation and preliminary screening of sgRNAs near the CpG islands.

[0157] The coding sequence of the self-cleaving peptide P2A used in this example is:

[0158] The coding sequence of EGFP used is:

[0159] The screening scheme for sgRNA functional verification using the above-mentioned reporter cell line is designed as follows (Figure 1B): After the reporter cells are plated, the composition EPIREG described in the present application (the domain of the composition is DNMT3A-hDNMT3L-xten80-ZIM3-xten80-dCas9, whose amino acid sequence is shown in SEQ ID NO: 1194, and its nucleic acid sequence is shown in SEQ ID NO: 1192 (CDS sequence) and 1193 (plasmid sequence)) containing different sgRNAs is delivered into the cells by transfection, and the two carry red fluorescence and blue fluorescence, respectively. The red fluorescent and blue fluorescent double positive cell populations are sorted by flow cytometry and cultured for a long time. Flow analysis is performed every other week to detect changes in the fluorescence intensity of the reporter cells, which can reflect changes in protein expression levels after epigenetic editing.

[0160] (3) Analysis of experimental results

[0161] The results shown in Figures 2A-2F show that 14 days after transfection with the composition described in the present application containing different sgRNAs, the fluorescence intensity of the HBx reporter cell line of type B HBV showed a significant decrease, indicating that HBx expression was significantly inhibited. On the 21st day after transfection, the results of each cell line were basically maintained, indicating that the inhibitory effect of epigenetic editing was maintained. This example summarizes the editing ability of each sgRNA in the cell line at different time points. Among them, BSG30, BSG35, BSG43, and BSG50 all have extremely high editing effects and target relatively concentrated areas in the genome. Figure 2G shows the relationship between the target position of the tested sgRNA in the type B HBV genome and the proportion of cells that can be knocked down on the 28th day after transfection. The results show that the sgRNAs with better knockdown effects are mainly concentrated in the areas near the BSG35 and BSG29 target sequences, indicating that epigenetic editing of this part of the region can better achieve the inhibition of HBx expression.

[0162] Figures 3A-3B show that the fluorescence intensity of the HBx reporter cell line transfected with HBV C decreased significantly on day 14 after transfection, indicating that HBx expression was significantly inhibited. Figure 3C shows the relationship between the targeted locations of the tested sgRNAs in the HBV C genome and the proportion of knockdown cells on day 14 after transfection. The results show that sgRNAs with good knockdown effects are mainly concentrated in the regions flanking the target sequences of BSG35, SG75, and BSG29, indicating that epigenetic editing in these regions can effectively inhibit HBx expression.

[0163] The transfection results of the HBx reporter cell line of type D HBV shown in Figures 4A-4F show that the fluorescence intensity decreased significantly on the 16th day after transfection, indicating that the expression of HBx was significantly inhibited. On the 21st and 28th days after transfection, the results of each cell line were basically maintained, indicating that the inhibitory effect of epigenetic editing was maintained. Figure 4G shows the relationship between the target position of the tested sgRNA in the type D HBV genome and the proportion of knockdown cells on the 28th day after transfection. The results show that the sgRNAs with better knockdown effects are mainly concentrated in the areas near the BSG35 and BSG29 target sequences, indicating that epigenetic editing of this part of the region can effectively inhibit HBx expression.

[0164] Based on the transfection results of the three genotypes of HBx reporter cell lines, the use of the epigenetic editing tools provided in this application to target the B, C, and D HBV genomes can significantly inhibit the expression of HBx, and this inhibitory effect is long-term, lasting at least 28 days. BSG29, BSG31, BSG34, and BSG35, which can simultaneously target three genomes, have a near-optimal inhibitory effect on the expression of HBx in all three genotypes of HBV. In the cell lines of the three genotypes, the sgRNAs with the best editing effects are mainly concentrated in the regions on both sides of the BSG35 and BSG29 target sequences, indicating that this part of the region may be the key region for epigenetic regulation of the HBV gene.

[0165] The sgRNAs that have been functionally verified in this example are summarized in the following table (arranged by the starting position of the target sequence of each sgRNA):

[0166] Example 2

[0167] The knockdown effect of the composition of the present application on HBV markers in primary hepatocytes (PHH)

[0168] This example uses a primary hepatocyte (PHH) cell line infected with hepatitis B virus type D (GenBank: U95551). Based on the results of the HBx reporter cell line screening described in Example 1, BSG29, BSG31, BSG34, and BSG35 are located in conserved regions of the genome and exhibit the best inhibitory effects. Therefore, these four sgRNAs were used to formulate the pharmaceutical composition provided herein and perform epigenetic editing in primary hepatocytes to verify their inhibitory effects on HBV gene expression.

[0169] The experimental scheme is shown in Figure 5A. Two days after primary hepatocytes were infected with HBV, lipid nanoparticles (LNPs) (LNP preparation reference: https: / / doi.org / 10.1038 / s41586-021-03534-y) were used to deliver a composition of mRNA encoding EPIREG (SEQ ID NO: 1191) and each sgRNA (BSG29, BSG31, BSG34, BSG35) into primary hepatocytes (dosage dose was 2.5 ug / ml, the mass ratio of EPIREG and sgRNA was 1:1). The culture supernatant was collected every two days after administration to detect the expression levels of HBV surface antigen (HBsAg) and core antigen (HBcAg) secreted by the cells. Cell samples were collected until 14 days after administration, DNA and RNA were extracted from the cells, and the levels of HBV mRNA and changes in the cccDNA of the HBV gene were detected. The two positive controls used Myrcludex B (WuXi AppTec, C9023GE070-1 / PE0723) and RG7834 (WuXi AppTec, ET25747-14-P1), respectively. Myrcludex B inhibits HBV infection of hepatocytes, while RG7834 inhibits the synthesis of viral proteins. RG7834 was discontinued on day 13 of the experiment to observe the rebound of viral antigen proteins. (Specific detection methods were performed according to the following kit instructions: HBsAg ELISA kit, Antu-CL 0310; HBeAg ELISA kit, Antu-CL 0312; RNeasy 96 Kit (12), QIAGEN #74182)

[0170] The experimental results 2 days, 4 days, 6 days, 8 days and 10 days after administration are summarized in Figure 5B. After delivering the composition containing BSG29, BSG31, BSG34, BSG35, BSG34+BSG35 (the mass ratio of EPIREG and sgRNA in BSG34+BSG35 is 1:0.5:0.5) to HBV-infected primary hepatocytes, the expression levels of HBsAg and HBeAg / HBcAg in the supernatant showed different degrees of decrease, among which BSG35 had the best effect, which could simultaneously reduce the expression levels of HBsAg and HBeAg / HBcAg by about 80%. Moreover, the combination of two sgRNAs (BSG34+BSG35) can further enhance the inhibitory effect and further reduce the expression levels of HBsAg and HBeAg / HBcAg. In the control group, HBsAg and HBeAg / HBcAg expression levels continued to rise with increasing infection days, reaching peaks around the 14th and 12th days post-infection, respectively. In the BSG35 experimental group, HBsAg and HBeAg / HBcAg expression levels remained essentially stable on the fourth day after administration. The inhibitory effect of the BSG35 experimental group was similar to that of two reference inhibitors, Myrcludex B and RG7834. Furthermore, after discontinuation of RG7834, a significant rebound (increased) trend in HBsAg and HBeAg / HBcAg expression was observed. In the BSG35 experimental group, no subsequent drug administration occurred 4 hours after drug treatment on the day of administration, and viral antigen protein levels remained stable at a low level throughout the experimental period. These results demonstrate that epigenetic editing can significantly reduce viral protein expression in HBV-infected PHHs, and that epigenetic editing using a single sgRNA can simultaneously regulate the expression of multiple viral proteins.

[0171] Example 3

[0172] sgRNA lentiviral library construction and functional screening

[0173] This example uses D-type HBV X protein (HBx), core antigen (HBcAg) and surface antigen (HBsAg) reporter cell lines for library screening. First, according to the method described in Example 1, a sgRNA cell library of the D-type HBV gene is constructed using a reporter cell line. The sgRNA library is packaged into a lentivirus to obtain an sgRNA lentiviral library (carrying red fluorescence), the lentiviral library is infected with a reporter cell line, and the red fluorescence is sorted to obtain an sgRNA cell library. Each cell in the sorted cell library integrates an sgRNA in the library, and at the same time, it carries a reporter sequence (carrying green fluorescence). The EPIREG tool described in Example 2 (the amino acid sequence of the tool is: SEQ ID NO: 1194) (carrying blue fluorescence) is transfected and delivered to a cell library carrying both sgRNA and reporter sequences. The red / green / blue fluorescent Sanyang cells are sorted using a flow cytometer and cultured for a long time. The EPIREG transfected into the cell can silence the GFP in the reporter together with the sgRNA. On day 14 after transfection, the GFP-negative cell population in the cell library was sorted, and genomic DNA from the negative cell population was extracted for NGS sequencing. Using the untreated cell library as a reference, the sgRNAs with increased sequencing reads in the negative cell population were compared to identify candidate sgRNAs with editing potential for each reporter. (A schematic diagram of this screening scheme is shown in Figure 6, and the analysis method is based on the literature DOI: 10.1186 / s13059-014-0554-4.) The following table summarizes the functionally validated sgRNAs for each reporter cell line (arranged by the starting position of each sgRNA's target sequence).

[0174] The information of sgRNA obtained by HBx reporter screening (as shown in the upper figure of Figure 7) is summarized as follows: Note: Log2 FC stands for fold change, which is the logarithm of the expression ratio between two samples (groups) to the base 2. It is used to indicate the differential expression level between the two. For example, a Log2 FC absolute value greater than 1 is usually used as the default screening criterion for differentially expressed genes.

[0175] The information of the sgRNA obtained by HBcAg reporter screening (as shown in the middle figure of Figure 7) is summarized as follows:

[0176] The information of sgRNA obtained by HBsAg reporter screening (as shown in the lower figure of Figure 7) is summarized as follows:

[0177] Example 4

[0178] Candidate sgRNA effect verification experiment screened by library

[0179] Effect validation in primary hepatocytes (PHH)

[0180] This validation experiment used a primary hepatocyte (PHH) cell line (WuXi AppTec, M00995-P) infected with hepatitis B virus type D (GenBank: U95551). Based on the screening results of the three libraries in Example 3 and factors such as conservation, the 20 sgRNAs shown in the table below were selected to formulate the pharmaceutical composition provided herein and perform epigenetic editing in the primary hepatocytes to verify the inhibitory effect of the selected candidate sgRNAs on HBV gene expression.

[0181] The 20 sgRNA sequences used for verification in this example are as follows:

[0182] The experimental scheme is shown in Figure 5A. Two days after primary hepatocytes were infected with HBV, lipid nanoparticles (LNPs) (LNP preparation reference: https: / / doi.org / 10.1038 / s41586-021-03534-y) were used to deliver the mRNA encoding EPIREG (sequence: SEQ ID NO: 1191) and each of the above-mentioned sgRNAs into primary hepatocytes (dosage dose was 2.5 ug / ml, the mass ratio of EPIREG and sgRNA was 1:1). Myrcludex B (provided by WuXi AppTec, C9023GE070-1 / PE0723) was used as a positive control. Myrcludex B can inhibit HBV infection of hepatocytes. After administration, the culture supernatant was collected every two days from each group to detect the expression levels of HBV surface antigen (HBsAg), core antigen (HBcAg / HBeAg), and HBV DNA secreted by the cells. Cell samples were collected 14 days after infection, DNA and RNA were extracted from the cells, and HBV mRNA levels were detected. (Specific detection methods were performed according to the instructions of the following kits: HBsAg ELISA kit, Antu-CL 0310; HBeAg ELISA kit, Antu-CL 0312; RNeasy 96 Kit (12), QIAGEN #74182)

[0183] The experimental results 14 days after infection are summarized in Figure 8. After delivering the combination of 20 sgRNAs and EPIREG to HBV-infected primary hepatocytes, the HBsAg, HBeAg / HBcAg and HBV in the supernatant were significantly increased. The expression levels of DNA showed varying degrees of decrease, of which 17 sgRNAs could reduce the expression of HBV viral antigens and DNA by more than 50% (except D409, D199, and D16), and the inhibition rate of 9 sgRNAs could reach nearly 80% or more (D340, D75, D97, D99, D100, D101, D108, D111, and D113), of which D99 ​​(i.e., BSG35) showed the highest inhibition level; EPIREG showed the same efficiency and trend in the inhibition of HBV total RNA and pgRNA as HBV antigens and DNA, indicating that the epigenetic editing tool effectively inhibited HBV transcription; at the same time, the combination of 20 sgRNAs and EPIREG did not affect the viability of PHH cells, indicating the safety of the epigenetic editing tool. In summary, through verification in the PHH cell line, most of the candidate sgRNAs obtained by library screening showed a significant inhibitory effect on HBV.

[0184] Knockdown effect of the composition on HBV markers in transgenic HBV mice

[0185] This validation experiment used transgenic HBV mice (Beijing Weitongda Biotechnology Co., Ltd., C57BL / 6-HBV, with subsequent breeding and testing performed by Beijing Weitongda). This strain of mice had a 1.28-fold HBV genome (type A, GenBank: AF305422.1) inserted into its genome. Based on all screening results, the sgRNA numbered D99 (BSG35) was located in a conserved region of the genome and exhibited the best inhibitory effect. Therefore, this sgRNA was used to formulate the pharmaceutical composition provided in this application and perform epigenetic editing in transgenic HBV mice to verify the inhibitory effect of this drug on integrated HBV gene expression in an in vivo model.

[0186] A combination of EPIREG mRNA (SEQ ID NO: 1191) and sgRNA D99 (BSG35) (mRNA:sgRNA mass ratio of 1:1) was delivered to transgenic HBV mice via tail vein injection of lipid nanoparticles (LNP) (LNP preparation reference: https: / / doi.org / 10.1038 / s41586-021-03534-y) at a dose of 10 mg / kg. A negative control was injected with PBS (200 μl), and a positive control was administered with the antisense oligonucleotide (ASO) drug Bepirovirsen (GSK3228836, dosed at 200 mg / kg), which targets all HBV RNA and thus reduces HBV antigen expression. Blood samples were collected regularly after administration to measure serum levels of secreted HBV surface antigen (HBsAg) and core antigen (HBcAg / HBeAg). HBV DNA levels were also measured using qPCR. (Hepatitis B virus e antigen quantitative kit: Mike Biotech, catalog number IM4403003; Hepatitis B virus surface antigen quantitative kit: Mike Biotech, catalog number IM4403001; Hepatitis B virus nucleic acid quantitative kit: Shengxiang Biotech, 2015340008; detection method is carried out according to the kit instructions).

[0187] The results of the post-administration experiments are summarized in Figures 9A-9C. Following a single injection of EPIREG, serum HBsAg, HBeAg, and HBV DNA expression levels in transgenic HBV mice rapidly decreased within one week, with the magnitude of the decrease approaching or exceeding that of the ASO group. However, HBV markers in the ASO group gradually returned to their original levels, while HBV markers in the EPIREG group were stably and persistently suppressed, with HBsAg and HBV DNA continuing to decrease approximately two months after administration (Figure 9A). Analysis of the HBV marker expression curves for each mouse in the EPIREG group (Figure 9B) revealed that, after a single injection of EPIREG, HBsAg and HBV DNA levels spontaneously decreased further in all three mice approximately two months after administration, with HBsAg decreasing to the lower limit of detection. Furthermore, progressive HBsAb expression was detectable in the serum of these three mice (Figure 9C). This result shows that in a transgenic HBV mouse model, the epigenetic editing composition comprising mRNA encoding EPIREG and the sgRNA provided in this application can significantly and persistently silence the expression of the integrated HBV genome in vivo, and due to the long-term silencing of HBV, the mice can gradually restore their immune response to the surface antigen HBsAg, thereby further reducing the expression of HBV markers.

[0188] Knockdown effect of the composition on HBV markers in AAV-HBV mice

[0189] This validation experiment used an AAV-HBV mouse model (modeling, subsequent breeding, and testing were completed by Beijing Weitongda Biotechnology Co., Ltd.). Adenovirus-associated viruses (AAV) carrying a 1.3-fold longer HBV genome (type D, GenBank: U95551) were used to infect mice to simulate the expression of free HBV genomes in vivo. Based on all screening results, the sgRNA numbered D99 (BSG35) is located in the conserved region of the genome and exhibits the best inhibitory effect. Therefore, this sgRNA was used to formulate the pharmaceutical composition provided in this application and perform epigenetic editing in AAV-HBV mice to verify the inhibitory effect of this drug on free HBV gene expression in an in vivo model.

[0190] Two titers (1E10 and 1E11) of AAV (AMV-002, Beijing Wujiahe Gene Technology Co., Ltd.) carrying 1.3 times the length of the HBV genome were delivered to mice via tail vein injection to achieve different degrees of stable expression of the HBV genome in vivo. Subsequently, on the day of the first dose (D0) and day 15 (D15), lipid nanoparticles (LNPs) (LNP preparation reference: https: / / doi.org / 10.1038 / s41586-021-03534-y) were injected into AAV-HBV mice via tail vein injection to deliver a combination of mRNA encoding EPIREG (sequence: SEQ ID NO: 1191) and sgRNA numbered D99 (BSG35) (mRNA:sgRNA mass ratio of 1:1) (both injection doses were 5 mg / kg). Negative controls were injected with PBS (200 μl). Blood was collected regularly after administration in each group to detect the levels of HBV surface antigen (HBsAg) and core antigen (HBcAg / HBeAg) secreted in the serum, and the level of HBV DNA was detected by qPCR (all detection kits are as described in the previous part of this example).

[0191] A summary of the post-dose experimental results is shown in Figure 10. After two injections of EPIREG in AAV-HBV mice, serum HBsAg, HBeAg, and HBV DNA expression levels rapidly decreased. The 1E10 AAV group exhibited low viral expression, with viral markers reduced to near the limit of detection within a short period of time after administration. The 1E11 AAV group exhibited high viral expression, with even greater reductions in viral markers achieved after administration. Ultimately, this epigenetic editing tool stably and persistently reduced HBV markers in both the 1E10 and 1E11 AAV groups. These results demonstrate that epigenetic editing can significantly and persistently silence episomal HBV genome expression in vivo in the AAV-HBV mouse model.

Claims

1. A composition comprising: (1) a fusion molecule or a nucleic acid sequence encoding the fusion molecule, wherein the fusion molecule comprises at least one DNA binding protein and at least one gene expression regulator, and (2) at least one single guide RNA (sgRNA), or a nucleic acid sequence encoding the sgRNA, The sgRNA is complementary to a target DNA sequence near a hepatitis B virus (HBV) gene and / or within a HBV gene regulatory element, the HBV gene is a type B HBV gene comprising a nucleotide sequence shown in SEQ ID NO: 1, a type C HBV gene comprising a nucleotide sequence shown in SEQ ID NO: 2, or a type D HBV gene comprising a nucleotide sequence shown in SEQ ID NO: 3, the HBV gene regulatory element comprises a transcription start site, a core promoter, a promoter, an enhancer, a silencer, an insulator element, a boundary element and / or a locus control region, and the target DNA sequence is located between nucleotides 1056 and 2354, between nucleotides 2639 and 2658, between nucleotides 2863 and 2930, and / or between nucleotides 3048 and 3067 of the HBV gene.

2. The composition according to claim 1, wherein the target DNA sequence is located between nucleotides 1056 and 1900, between nucleotides 1972 and 2082, between nucleotides 2134 and 2264, between nucleotides 2335 and 2354, between nucleotides 2639 and 2658, between nucleotides 2863 and 2930, and / or between nucleotides 3048 and 3067 of the HBV gene.

3. The composition according to claim 1 or 2, wherein the target DNA sequence is located between nucleotides 1060 to 1079, between nucleotides 1149 to 1612, between nucleotides 1693 to 1852, and / or between nucleotides 2863 to 2882 of the HBV gene.

4. The composition according to any one of claims 1-3, wherein the target DNA sequence is located in one or more regions of the following type B HBV gene: between nucleotides 1149 and 1190, between nucleotides 1210 and 1310, between nucleotides 1350 and 1400, between nucleotides 1420 and 1450, and between nucleotides 1470 and 1592.

5. The composition according to any one of claims 1-3, wherein the target DNA sequence is located in one or more regions of the following type C HBV gene: between nucleotides 1150 and 1180, between nucleotides 1200 and 1310, between nucleotides 1350 and 1390, between nucleotides 1420 and 1460, and between nucleotides 1480 and 1593.

6. The composition according to any one of claims 1-3, wherein the target DNA sequence is located in one or more regions of the following D-type HBV gene: between nucleotides 1056 and 1079, between nucleotides 1101 and 1900, between nucleotides 1972 and 2082, between nucleotides 2134 and 2264, between nucleotides 2335 and 2354, between nucleotides 2639 and 2658, between nucleotides 2863 and 2882, between nucleotides 2911 and 2930, and between nucleotides 3048 and 3067.

7. The composition according to any one of claims 1-3 and 6, wherein the target DNA sequence is located in one or more regions of the following D-type HBV gene: between nucleotides 1060 and 1079, between nucleotides 1160 and 1310, between nucleotides 1253 and 1284, between nucleotides 1370 and 1470, between nucleotides 1490 and 1612, between nucleotides 1693 and 1852, and between nucleotides 2863 and 2882.

8. The composition according to any one of claims 1-7, wherein the sgRNA comprises a nucleotide sequence shown in any one of SEQ ID NOs: 4-1165.

9. The composition according to any one of claims 1 to 7, wherein the sgRNA comprises a partial sequence of the nucleotide sequence shown in any one of SEQ ID NOs: 4 to 1165, and the length of the partial sequence is 15 to 20 base pairs.

10. The composition of any one of claims 1-9, wherein the at least one DNA binding protein is a CRISPR enzyme, a zinc finger nuclease (ZNF), a transcription activator-like effector nuclease (TALEN), a homing endonuclease, a dCas9-FokI nuclease, or a MegaTal nuclease.

11. The composition of claim 10, wherein the CRISPR enzyme is a class 2 Cas protein and / or a mutant thereof.

12. The composition of claim 10 or 11, wherein the CRISPR enzyme is one or more of the following Cas proteins: class 2 type II-A Cas protein, class 2 type II-B Cas protein, class 2 type II-C Cas protein, class 2 type VA Cas protein, class 2 type VB Cas protein, class 2 type VC Cas protein, class 2 type VU Cas protein, and mutants thereof.

13. The composition according to any one of claims 10-12, wherein the CRISPR enzyme is a Cas9 protein and / or a mutant thereof.

14. The composition of any one of claims 1-13, wherein the at least one DNA binding protein is dCas9.

15. The composition of claim 14, wherein the dCas9 comprises Staphylococcus aureus dCas9, Streptococcus pyogenes dCas9, Campylobacter jejuni dCas9, Corynebacterium diphtheria dCas9, Eubacterium ventriosum dCas9, Streptococcus pasteurianus dCas9, Lactobacillus farciminis dCas9, Sphaerochaeta globus dCas9, Azospirillum (e.g., strain B510) dCas9, Gluconacetobacter diazotrophicus dCas9, Neisseria griseus dCas9, cinerea dCas9, Roseburia intestinalis dCas9, Parvibaculum lavamentivorans dCas9, Nitratifractor salsuginis (e.g., strain DSM 16511) dCas9, Campylobacter lari (e.g., strain CF89-12) dCas9, Streptococcus thermophilus (e.g., strain LMD-9) dCas9.

16. The composition according to claim 14 or 15, wherein the dCas9 comprises the amino acid sequence shown in SEQ ID NO: 1170-1187.

17. The composition according to any one of claims 1-16, wherein the at least one gene expression regulator provides modification of at least one nucleotide near the HBV gene and / or within the HBV gene regulatory element.

18. The composition of any one of claims 1-17, wherein the at least one gene expression regulator comprises one or more selected from the group consisting of DNA methyltransferases, DNA hydroxymethylases, DNA demethylases, histone methyltransferases, histone demethylases, histone acetyltransferases, histone deacetylases, phosphatases, kinases, transcriptional activators, transcriptional repressors, parts of the foregoing, and any combination of the foregoing.

19. The composition of claim 17, wherein the modification of the at least one nucleotide is DNA methylation.

20. The composition of any one of claims 1-19, wherein the at least one gene expression regulator comprises one or more selected from DNA methyltransferases (DNMTs), zinc finger protein-based transcription factors, the moieties described above, and any combination thereof.

21. The composition of any one of claims 1-20, wherein the at least one gene expression regulator comprises a DNA methyltransferase (DNMT) or a portion thereof, and a zinc finger protein-based transcription factor or a portion thereof.

22. The composition of claims 18, 20 and 21, wherein the DNA methyltransferase is DNMT3A, DNMT3B, DNMT3L, DNMT1 or DNMT2.

23. The composition according to claim 22, wherein the DNMT3A comprises the amino acid sequence shown in SEQ ID NO: 1166, and the DNMT3L comprises the amino acid sequence shown in SEQ ID NO: 1167 or 1195.

24. The composition according to claim 20 or 21, wherein the zinc finger protein-based transcription factor is Krüppel-related repressor (KRAB) or a KRAB domain derived from ZIM3 (ZIM3 KRAB).

25. The composition according to claim 24, wherein the zinc finger protein-based transcription factor comprises the amino acid sequence shown in SEQ ID NO: 1168 or 1196.

26. The composition of any one of claims 18 and 20-25, wherein the DNA methyltransferase is selected from DNMT3A and DNMT3L and combinations thereof, and the zinc finger protein-based transcription factor is KRAB or ZIM3 KRAB.

27. The composition of any one of claims 1-26, wherein the fusion molecule comprises the at least one gene expression regulator fused to the C-terminus, N-terminus, or both ends of the at least one DNA binding protein.

28. The composition of any one of claims 1-27, wherein the at least one gene expression regulator is directly fused to the at least one DNA binding protein.

29. The composition of any one of claims 1-27, wherein the at least one gene expression regulator is indirectly fused to the at least one DNA binding protein via a non-regulator, a second regulator, or a linker.

30. The composition of any one of claims 1-29, wherein the fusion molecule comprises the domain DNMT3A-DNMT3L-dCas9-KRAB or the domain DNMT3A-DNMT3L-ZIM3 KRAB-dCas9, in, - indicates that the partial domains of the fusion molecule are directly and / or indirectly connected, and the partial domains are in the order from N-terminus to C-terminus.

31. The composition according to any one of claims 1-30, wherein the fusion molecule comprises the amino acid sequence shown in SEQ ID NO: 1169 or 1194.

32. The composition of any one of claims 1-31, wherein the fusion molecule further comprises at least one nuclear localization sequence (NLS).

33. The composition of claim 32, wherein the at least one nuclear localization sequence is fused directly or indirectly to the C-terminus, N-terminus, or both of the at least one DNA binding protein.

34. The composition of any one of claims 1-33, wherein the nucleic acid sequence encoding the fusion molecule is deoxyribonucleic acid (DNA) or messenger ribonucleic acid (mRNA).

35. The composition of any one of claims 1-34, wherein the fusion molecule is packaged in a liposome or a lipid nanoparticle.

36. The composition of any one of claims 1-35, wherein the fusion molecule and the sgRNA are packaged in a liposome or a lipid nanoparticle.

37. The composition according to any one of claims 1-36, wherein the fusion molecule and the sgRNA are packaged in the same liposome or lipid nanoparticle, or in different liposomes or lipid nanoparticles.

38. The composition of any one of claims 1-37, wherein the liposome or the lipid nanoparticle comprises ionizable lipids (20%-70%, molar ratio), pegylated lipids (0%-30%, molar ratio), supporting lipids (30%-50%, molar ratio) and cholesterol (10%-50%, molar ratio).

39. The composition of claim 38, wherein the ionizable lipid is selected from the group consisting of a pH-responsive ionizable lipid, a thermally responsive ionizable lipid, and a light-responsive ionizable lipid.

40. The composition of any one of claims 1-34, wherein the fusion molecule is packaged in an AAV vector.

41. The composition of any one of claims 1-34 and 40, wherein the fusion molecule and the sgRNA are packaged in an AAV vector.

42. The composition of any one of claims 1-34, 40 and 41, wherein the fusion molecule and the sgRNA are packaged in the same AAV vector or different AAV vectors.

43. The composition according to any one of claims 1-42, which is a pharmaceutical composition comprising a pharmaceutically acceptable carrier.

44. A single guide RNA (sgRNA), the sgRNA comprising a sequence complementary to a target DNA sequence, the target DNA sequence being located near a hepatitis B virus (HBV) gene and / or within a HBV gene regulatory element; the HBV gene being a type B HBV gene comprising a nucleotide sequence shown in SEQ ID NO: 1, a type C HBV gene comprising a nucleotide sequence shown in SEQ ID NO: 2, or a type D HBV gene comprising a nucleotide sequence shown in SEQ ID NO: 3, the HBV gene regulatory element comprising a transcription start site, a core promoter, a promoter, an enhancer, a silencer, an insulator element, a boundary element and / or a locus control region, and the target DNA sequence being located between nucleotides 1056 and 2354, between nucleotides 2639 and 2658, between nucleotides 2863 and 2930, and / or between nucleotides 3048 and 3067 of the HBV gene.

45. The sgRNA according to claim 44, wherein the target DNA sequence is located between nucleotides 1056 and 1900, between nucleotides 1972 and 2082, between nucleotides 2134 and 2264, between nucleotides 2335 and 2354, between nucleotides 2639 and 2658, between nucleotides 2863 and 2930, and / or between nucleotides 3048 and 3067 of the HBV gene.

46. ​​According to the sgRNA of claim 44 or 45, the target DNA sequence is located between nucleotides 1060 to 1079, between nucleotides 1149 to 1612, between nucleotides 1693 to 1852, and / or between nucleotides 2863 to 2882 of the HBV gene.

47. According to the sgRNA of any one of claims 44-46, the target DNA sequence is located in one or more regions of the following type B HBV gene: between nucleotides 1149 and 1190, between nucleotides 1210 and 1310, between nucleotides 1350 and 1400, between nucleotides 1420 and 1450, and between nucleotides 1470 and 1592.

48. According to the sgRNA of any one of claims 44-46, the target DNA sequence is located in one or more regions of the following C-type HBV gene: between nucleotides 1150 and 1180, between nucleotides 1200 and 1310, between nucleotides 1350 and 1390, between nucleotides 1420 and 1460, and between nucleotides 1480 and 1593.

49. According to the composition described in any one of claims 44-46, the target DNA sequence is located in one or more regions of the following D-type HBV gene: between nucleotides 1056 and 1079, between nucleotides 1101 and 1900, between nucleotides 1972 and 2085, between nucleotides 2134 and 2264, between nucleotides 2335 and 2354, between nucleotides 2639 and 2658, between nucleotides 2863 and 2882, between nucleotides 2911 and 2930, and between nucleotides 3048 and 3067.

50. According to the sgRNA of any one of claims 44-46 and 49, the target DNA sequence is located in one or more regions of the following D-type HBV gene: between nucleotides 1060 and 1079, between nucleotides 1160 and 1310, between nucleotides 1253 and 1284, between nucleotides 1370 and 1470, between nucleotides 1490 and 1612, between nucleotides 1693 and 1852, and between nucleotides 2863 and 2882.

51. The sgRNA according to any one of claims 44-50, comprising a nucleotide sequence shown in any one of SEQ ID NOs: 4-1165.

52. The sgRNA according to any one of claims 44 to 50, wherein the sgRNA comprises a partial sequence of the nucleotide sequence shown in any one of SEQ ID NOs: 4 to 1165, and the length of the partial sequence is 15 to 20 base pairs.

53. A nucleic acid molecule encoding the sgRNA of any one of claims 44-52.

54. A method for reducing or eliminating the expression of hepatitis B virus (HBV) gene products in cells, the method comprising the step of introducing the composition of any one of claims 1-43 into the cells, thereby reducing or eliminating the expression of the HBV gene products in the cells.

55. A method for reducing or eliminating the expression of hepatitis B virus (HBV) gene products in a subject in vivo, the method comprising the step of introducing the composition described in any one of claims 1-43 into the cells of the subject, thereby reducing or eliminating the expression of the HBV gene products in the subject.

56. A method for treating a disease associated with hepatitis B virus (HBV) infection in a subject or alleviating the symptoms of a disease associated with HBV infection in a subject, the method comprising the step of introducing an effective amount of the composition described in any one of claims 1-43 into cells of the subject.

57. The method of claim 55 or 56, wherein the subject is a mammal, such as a human, monkey, mouse, rat, rabbit, pig, horse, cat, and dog.

58. The method of any one of claims 55-57, comprising administering the composition to the subject one or more times.

59. The method of any one of claims 55-58, comprising administering the composition to the subject at least twice.

60. The method of any one of claims 55-59, wherein the interval between administering the composition more than once or administering the composition at least twice is 1 day, 2 days, 3 days, 4 days, 5 days, 6 days, 7 days, 8 days, 9 days, 10 days, 11 days, 12 days, 13 days, 14 days or 15 days.

61. The method according to claim 56, wherein the HBV infection-related diseases include hepatitis, cirrhosis, liver fibrosis and hepatocellular carcinoma caused by HBV infection.

62. The composition of any one of claims 1-43, which is used to treat a disease associated with hepatitis B virus (HBV) infection in a subject or alleviate the symptoms of a disease associated with HBV infection in a subject.

63. A kit comprising the composition of any one of claims 1-43 and a container for placing the composition and / or instructions for use.

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