WO2022215982A1 - Guide rna complementary to trac gene and use thereof - Google Patents

Abstract

The present invention relates to a guide RNA complementary to the TRAC gene and a use thereof. A guide RNA according to one aspect, a vector comprising same, and a TRAC gene editing composition, comprising the guide RNA and a Cas9 editor protein or a variant thereof, can effectively knock out the TRAC gene from the genome of a cell or an individual and thus can be useful in preventing or treating cancer through personalized medicine or precision medicine.

Description

Guide RNA complementary to TRAC gene and uses thereof

It relates to a guide RNA complementary to a TRAC gene and uses thereof.

Gene scissors refers to an enzyme that binds to a gene and cuts a specific DNA region, or a genome editing technique using the same. Using gene scissors, it can be used in various fields such as correction of mutations that cause genetic diseases in stem cells or somatic cells, and anticancer cell therapy. The gene editing technology has evolved into the first generation zinc finger nuclease (ZFN), the second generation TALEN (transcription activator-like effector nuclease), and the third generation CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats)/Cas9.

CRISPR gene scissors (CRISPR/Cas9) consists of a guide RNA and Cas9 nuclease having specific nucleotide sequence information of the targeted DNA, and delivers it into the cell to cut a gene at a desired location or remove an existing gene. and insert new genes. When cleaving specific DNA using gene scissors, Cas9 nuclease cleaves the DNA target sequence specified by the sequence of the guide RNA. A method of editing a genome using gene scissors is known through a number of documents such as Korean Publication No. 10-2015-0101478. Recently, Cas9 variants with increased accuracy have been developed to reduce the probability of off-target that cuts off-target points. Such high-fidelity variants include HypaCas9, SpCas9, evoCas9, eSpCas9, Sniper-Cas9, SpCas9-HF1, xCas9, and the like.

TRAC (T Cell Receptor Alpha Constant) is a gene that expresses TCR (T Cell Receptor), which is distributed on the surface of T cells, which are immune cells, and plays an essential role in the natural response of T cells to antigens as a membrane protein complex. TCR recognizes cancer cell antigens through a molecule called Major Histocompatibility Complex (MHC). Since MHC has a specific combination that differs from person to person, the TCR must precisely match the MHC molecule in order to recognize the antigen. Suppression of the occurrence of Graft-versus-Host Disease (GvHD) is the key in the development of allogeneic therapeutics, since the more different MHCs are, the more intense the rejection reaction. Therefore, the TRAC gene is an important treatment enemy target.

Therefore, there is a need to develop guide RNAs targeting the TRAC gene.

One aspect is to provide a guide RNA comprising a nucleic acid sequence identical to or complementary to a polynucleotide selected from the group consisting of SEQ ID NOs: 1 to 4.

Another aspect is to provide a CRISPR/Cas9 system comprising the guide RNA and the Cas9 editor protein or a variant thereof, and a recombinant vector comprising the same.

Another aspect is to provide a composition for TRAC gene editing comprising the guide RNA, the CRISPR / Cas9 system, and a recombinant vector comprising them.

Other objects and advantages of the present application will become more apparent from the following detailed description in conjunction with the appended claims and drawings. Content not described in this specification will be omitted because it can be sufficiently recognized and inferred by those skilled in the technical field or similar technical field of the present application.

Each description and embodiment disclosed in this application is also applicable to each other description and embodiment. That is, all combinations of the various elements disclosed in this application fall within the scope of this application. In addition, it cannot be seen that the scope of the present application is limited by the detailed description described below.

One aspect provides a guide RNA comprising a nucleic acid sequence identical to or complementary to one polynucleotide selected from the group consisting of SEQ ID NOs: 1 to 4.

As used herein, the term "guide RNA" refers to a polynucleotide that cuts, inserts, or connects a target DNA in a cell through RNA editing. The guide RNA may be a single-chain guide RNA (sgRNA). The guide RNA may be a crRNA (CRISPR RNA) specific for a target nucleic acid sequence. The guide RNA may further include a trans-activating crRNA (tracrRNA) that interacts with the Cas9 nuclease. The tracrRNA may include a polynucleotide forming a loop structure.

In general, a guide sequence is any polynucleotide sequence having sufficient complementarity with a target polynucleotide sequence to hybridize to the target sequence and induce sequence-specific binding of the CRISPR complex to the target sequence.

TRAC gene (T Cell Receptor Alpha Constant) is a gene that expresses TCR (T Cell Receptor), which is distributed on the surface of T cells, which are immune cells, and plays an essential role in the natural response of T cells to antigens as a membrane protein complex. TCR recognizes cancer cell antigens through a molecule called Major Histocompatibility Complex (MHC). Since MHC has a specific combination that differs from person to person, the TCR must precisely match the MHC molecule in order to recognize the antigen. Suppression of the occurrence of Graft-versus-Host Disease (GvHD) is the key in the development of allogeneic therapeutics, since the more different MHCs are, the more intense the rejection reaction. Therefore, the TRAC gene is an important treatment known as an enemy target. The TRAC gene is, for example, NCBI Accession No. currently registered in NCBI GenBank, respectively. It may correspond to NG_001332.3. Those skilled in the art will be able to easily identify the sequence using the sequence ID accession number. The specific sequence corresponding to the Sequence ID number registered in the UCSC genome browser or GenBank may be slightly changed over time. It will be apparent to those skilled in the art that the scope of the present invention also extends to such altered sequences.

In addition, any nucleotide sequence that can be used for genetic manipulation to reduce the expression or activity of the TRAC gene or the protein expressed by the TRAC gene can be used as a guide RNA without limitation, for example, the nucleotide sequence is a sequence capable of hybridizing with the TRAC gene. It may be, for example, one comprising a polynucleotide consisting of SEQ ID NOs: 1 to 4 or a nucleic acid sequence complementary thereto. In addition, a portion of the guide RNA nucleotide sequence may be modified in order to modify/enhance the function of the guide RNA. Also in some embodiments, the degree of complementarity between a guide sequence and its corresponding target sequence, when optimally aligned using an appropriate alignment algorithm, is about 50%, 60%, 75%, 80%, 85%, 90%, 95%, 97.5%, 99% or more. Optimal alignment can be determined using any algorithm suitable for aligning sequences, non-limiting examples of which include the Smith-Waterman algorithm, the Needleman-Wunsch algorithm, the Burroughs- Algorithms based on the Burrows-Wheeler Transform (eg Burrows Wheeler Aligner), ClustalW, Clustal X, BLAT, Novocraft Technologies, ELAND (Illumina), SOAP ( available at soap.genomics.org.cn) and Maq (available at maq.sourceforge.net).

The guide RNA may be 10 nucleotides to 30 nucleotides in length. The guide RNA has a length of, for example, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, or 30 nucleotides.

The guide RNA may include a nucleic acid sequence identical to or complementary to two or more consecutive polynucleotides in a nucleic acid sequence selected from the group consisting of SEQ ID NOs: 1 to 4. The guide RNA may include two or more consecutive polynucleotides complementary to the remaining nucleic acid sequences except for the PAM sequence among the target nucleic acid sequences selected from the group consisting of SEQ ID NOs: 1 to 4. The guide RNA may include a polynucleotide complementary to the remaining nucleic acid sequences except for the PAM sequence among the target nucleic acid sequences selected from the group consisting of 1 to 4.

In addition, in the guide RNA, the complementary nucleic acid sequence may include a polynucleotide into which one polynucleotide selected from the group consisting of SEQ ID NOs: 1 to 4 is transcribed.

The guide RNA may include RNA, DNA, PNA, or a combination thereof. The guide RNA may be chemically modified.

The guide RNA may hybridize with the TRAC gene, and specifically, the guide RNA may hybridize or bind to at least one site in the region consisting of exon 1 of the TRAC gene.

The guide RNA may be a component of a programmable nuclease. Genetic scissors refer to any type of nuclease that can cut by recognizing a specific position on the genome. The gene scissors are, for example, transcription activator-like effector nuclease (TALEN), zinc finger nuclease, meganuclease, RNA-guided endonuclease (RGEN), Cpf1 and allologs. (Ago homolog, DNA guided endonuclease). The RGEN refers to a nuclease comprising a guide RNA specific for a target DNA and a Cas protein as components. Said polynucleotide is, for example, a component of an RGEN.

Also, the guide RNA may induce modification in the nucleic acid sequence of the TRAC gene. The guide RNA may remove the nucleic acid sequence encoding the TRAC protein by non-homologous end-joining (NHEJ) from the genome of the cell. Specifically, the modification in the nucleic acid sequence includes 1) deletion of all or a continuous 1bp to 15bp nucleotide sequence region of the TRAC gene, 2) substitution of 1 to 15 nucleotides of the TRAC gene with nucleotides different from those of the wild-type gene, 3) each independently insertion into TRAC of 1 to 15 nucleotides selected from A, T, C and G, or 4) a combination of two or more selected from 1) to 3) above. Specifically, the deletion may be a deletion of a nucleotide sequence region of about 6 bp, 8 bp, 11 bp, and/or 13 bp of the TRAC gene, and the insertion is 1 bp, 4 bp, 6 bp, 8 bp, It may be an insertion of an 11 bp, or 13 bp, and/or 15 bp site.

One aspect is a nucleic acid sequence identical to or complementary to one polynucleotide selected from the group consisting of SEQ ID NOs: 1 to 4; and a Cas9 editor protein or variant thereof; or a CRISPR/Cas9 system comprising a nucleic acid sequence encoding the same.

In general, a “CRISPR system” refers to a sequence that collectively encodes a Cas gene, a tracr (trans-activating CRISPR) sequence (eg, tracrRNA or active moiety tracrRNA), a tracr-mate sequence (in the context of an endogenous CRISPR system, “ CRISPR-related (including direct repeats” and tracrRNA-processing portion direct repeats), guide sequences (also referred to as “spacers” in the context of endogenous CRISPR systems), guide RNAs or other sequences and transcripts from the CRISPR locus "Cas") refers to transcripts and other elements involved in the expression of or inducing its activity. In some embodiments, one or more elements of the CRISPR system are derived from a type I, type II, or type III CRISPR system. In some embodiments, one or more elements of the CRISPR system are derived from a particular organism comprising an endogenous CRISPR system, eg, Streptococcus pyogenes. In general, CRISPR systems are characterized by elements that promote the formation of CRISPR complexes at the site of the target sequence (also referred to as protospacers in the context of endogenous CRISPR systems). In the context of the formation of a CRISPR complex, a "target sequence" or "target gene" refers to a sequence to which a guide sequence is designed to have complementarity, wherein hybridization between the target sequence and the guide sequence enhances the formation of the CRISPR complex. Although essentially perfect complementarity is not required, there is sufficient complementarity to cause hybridization and promote formation of the CRISPR complex. The target sequence may comprise any polynucleotide, eg, a DNA or RNA polynucleotide. In some embodiments, the target sequence is located in the nucleus or cytoplasm of the cell.

When the Cas protein forms a complex with two RNAs called CRISPR RNA (crRNA) and trans-activating crRNA (tracrRNA), it forms an active endonuclease or nickase. Non-limiting examples of such Cas proteins include Cas1, Cas1B, Cas2, Cas3, Cas4, Cas5, Cas6, Cas7, Cas8, Cas9 (also known as Csn1 and Csx12), Cas10, Csy1, Csy2, Csy3, Cse1, Cse2, Csc1, Csc2, Csa5, Csn2, Csm2, Csm3, Csm4, Csm5, Csm6, Cmr1, Cmr3, Cmr4, Cmr5, Cmr6, Csb1, Csb2, Csb3, Csx17, Csx14, Csx16, CsX, Csx3, Csx10, Csx, Csx Csf2, Csf3, Csf4, homologues thereof or modified versions thereof. These enzymes are known; For example, the amino acid sequence of the Streptococcus pyogenes Cas9 protein can be obtained from the SwissProt database under accession number Q99ZW2. In some embodiments, the unmodified CRISPR enzyme, eg, Cas9, has DNA cleavage activity. In some embodiments, the CRISPR enzyme is Cas9, which may be Cas9 from Streptococcus pyogenes or Streptococcus pneumoniae. In some embodiments, the Cas protein is codon-optimized for expression in a eukaryotic cell.

The Cas protein is one of the protein components of the CRISPR/Cas system, and may be an activated endonuclease or a nick forming enzyme. The Cas protein may form a complex with crRNA (CRISPR RNA) and tracrRNA (trans-activating crRNA) to exhibit its activity.

The Cas protein may be, for example, from the genus Streptococcus (eg, Streptococcus pyogens), from the genus Neisseria (eg, Neisseria meningitidis), from the genus Pasteurella (eg, Pasteurella multocida), from the genus Francisella (eg, Francisella novicida), or It may be a polynucleotide derived from a bacterium of the genus Campylobacter (eg, Campylobacter jejuni). The Cas protein is GenBank Accession No. and the amino acid sequence of Q99ZW2.1.

The Cas protein may be a wild-type Cas protein or a mutant Cas protein. The mutant Cas protein may be, for example, a protein in which a catalytic aspartate residue is changed to another amino acid (eg, alanine). The Cas protein may be a recombinant protein.

The Cas protein may be a Cas9 protein or a Cpf1 protein.

The Cas9 protein may be a Cas9 protein variant. For example, although not limited thereto, the variant may be one or more selected from the group consisting of HypaCas9, SpCas9, evoCas9, eSpCas9, Sniper-Cas9, SpCas9-HF1 and xCas9. Among the Cas 9 protein variants, eSpCas9 may be translated from the sequence of the polynucleotide consisting of SEQ ID NO: 7, evoCas9 may be translated from the sequence of the polynucleotide consisting of SEQ ID NO: 8, HypaCas9 is the polynucleotide consisting of SEQ ID NO: 9 It may be translated from the sequence of nucleotides, Sniper-Cas9 may be translated from the sequence of the polynucleotide consisting of SEQ ID NO: 10, SpCas9 may be translated from the sequence of the polynucleotide consisting of SEQ ID NO: 11, SpCas9- HF1 may be translated from the sequence of the polynucleotide consisting of SEQ ID NO: 12, and xCas9 may be translated from the sequence of the polynucleotide consisting of SEQ ID NO: 13.

Another aspect is a nucleic acid sequence identical to or complementary to one polynucleotide selected from the group consisting of SEQ ID NOs: 1 to 4; and a Cas9 editor protein or variant thereof; Or it provides a recombinant vector comprising a nucleic acid sequence encoding the same. The vector may be introduced into a cell or subject to generate a guide RNA. The vector may be introduced into a cell or subject to express TRAC guide RNA and/or Cas protein to form an insertion/deletion site in a nucleic acid sequence encoding the TRAC protein in the cell or subject to induce mutation.

The term "polynucleotide" is a polymer of deoxyribonucleotides or ribonucleotides that exist in single-stranded or double-stranded form. It encompasses RNA genomic sequences, DNA (gDNA and cDNA) and RNA sequences transcribed therefrom, and includes analogs of natural polynucleotides, unless otherwise specified.

The polynucleotide includes not only a nucleotide sequence encoding the amino acid sequence of the fusion protein, but also a sequence complementary to the sequence. The complementary sequence includes not only perfectly complementary sequences, but also substantially complementary sequences, which under stringent conditions known in the art, for example, nucleotides encoding the amino acid sequence of the fusion protein. It refers to a sequence capable of hybridizing with the nucleotide sequence of the sequence.

The vector can be constructed through various methods known in the art.

The vector may be a vector for cloning or a vector for expression. The vector may be a viral vector, a plasmid vector, or an agrobacterium vector.

The vector can be constructed using a prokaryotic cell or a eukaryotic cell as a host. When the vector is an expression vector and a prokaryotic cell is used as a host, a strong promoter capable of propagating transcription (eg, tac promoter, lac promoter, lacUV5 promoter, lpp promoter, pLλ promoter, pRλ promoter, rac5 promoter, amp promoter, recA promoter, SP6 promoter, trp promoter and T7 promoter), a ribosome binding site for initiation of translation, and a transcription/translation termination sequence. When the vector is a vector for expression and the host is a eukaryotic cell, a promoter derived from the genome of a mammalian cell (eg, metallotionine promoter) or a promoter derived from a mammalian virus (eg, , adenovirus late promoter, vaccinia virus 7.5K promoter, SV40 promoter, cytomegalovirus promoter, and tk promoter of HSV) may be used, and may have a polyadenylation sequence as a transcription termination sequence. On the other hand, the vector is a plasmid often used in the art (eg pSC101, ColE1, pBR322, pUC, pUC8/9, pHC79, pUC19 and pET, etc.), phage (eg λgt4 λB, λ-Charon, λ Δz1 and M13) or viruses (eg, SV40, etc.). The vector may include a CBh promoter, a U6 promoter, a CMV promoter, an EF-1α promoter, or a combination thereof.

The recombinant vector can be constructed using a prokaryotic cell or a eukaryotic cell as a host. For example, when the vector of the present invention is an expression vector and a prokaryotic cell is used as a host, a strong promoter capable of propagating transcription (eg, pLλ promoter, trp promoter, lac promoter, tac promoter, T7 promoter, etc.) ), a ribosome binding site for initiation of translation and a transcription/translation termination sequence. In the case of a eukaryotic cell as a host, the replication origin operating in the eukaryotic cell contained in the vector includes the f1 origin of replication, the SV40 origin of replication, the pMB1 origin of replication, the adeno origin of replication, the AAV origin of replication and the BBV origin of replication. It is not limited. In addition, promoters derived from the genome of mammalian cells (eg, metallotionine promoter) or from mammalian viruses (eg, adenovirus late promoter, vaccinia virus 7.5K promoter, SV40 promoter, cytomegalovirus promoter and tk promoter of HSV) can be used, and generally have a polyadenylation sequence as a transcription termination sequence.

The vector may include an antibiotic resistance gene. The antibiotic resistance gene may include an ampicillin resistance gene, a puromycin resistance gene, chloramphenicol, a blasticidin resistance gene, or a combination thereof.

Another aspect is a guide RNA and a Cas9 editor protein or a variant thereof comprising a nucleic acid sequence identical to or complementary to one polynucleotide selected from the group consisting of SEQ ID NOs: 1 to 4; Or it provides a composition for TRAC gene editing comprising a nucleic acid sequence encoding the same.

The guide RNA, vector, TRAC protein, and nucleic acid sequences encoding the TRAC protein are as described above.

The composition may be for administration in vitro or in vivo .

When the composition is administered to cells in vitro or in vivo, expression or activity may be exhibited or reduced to a degree lower than the measured TRAC gene or expression or activity level of a protein encoded by the TRAC gene of the cell or individual, or The TRAC gene can be edited to inactivate it. This means that the expression or activity can be exhibited to a lower degree than the expression or activity level of the protein encoded by the TRAC gene of the cells or administered subject in vitro, or the expression or activity can be abolished. That is, in the cell, the gene editing by the composition shows that the expression or activity of the TRAC gene or the protein encoded by the TRAC gene is about 20% or more, about 30% or more, about 40% more than that of the original non-engineered parent cell. at least about 50%, at least about 55%, at least about 60%, at least about 70%, at least about 75%, at least about 80%, at least about 85%, at least about 90%, at least about 95%, or at least about 100 % can be reduced.

The composition is capable of editing the genome such that the nucleic acid sequence encoding the TRAC protein is altered in the genome of a cell, thereby inducing any modification that eliminates or reduces the function of the TRAC protein, i.e., deletion, substitution, insertion, or frameshift mutation. By inducing the TRAC gene can be effectively knocked out (knockout).

The cells may be selected from the group consisting of cancer cells, stem cells, vascular endothelial cells, leukocytes, immune cells, epithelial cells, germ cells, fibroblasts, myocytes, bone marrow cells, epidermal cells, osteoblasts and neurons.

Genetically engineered or edited cells with reduced expression or activity of the TRAC gene or the protein encoded by the TRAC gene can be identified using any method known in the art. The term “inactivation” may mean that a gene that is not expressed at all or a protein that has no activity even if it is expressed is generated. The term "depression" may mean that the TRAC gene is expressed at a low level compared to the non-engineered cells, or that the activity is low or the activity is removed even if the protein encoded by the TRAC gene is expressed.

The "removal" refers to any modification in which the function of the TRAC protein is eliminated or reduced by altering the nucleic acid sequence encoding the TRAC protein in the genome of a cell. The term “removal” may be used interchangeably with “mutation”. The deletion or mutation may be, for example, a deletion, substitution, insertion, or frameshift mutation.

The composition for gene editing can be genetically manipulated or edited to reduce the expression or activity of a protein encoded by the TRAC gene, and thus can be used for the prevention and/or treatment of cancer of an individual administered the composition.

A composition for TRAC gene editing comprising a guide RNA, a vector comprising the same, the guide RNA and Cas9 editor protein or a variant thereof according to an aspect can effectively knockout the TRAC gene from the genome of a cell or individual, It can be usefully used to prevent or treat cancer as personalized medicine or precision medicine.

1 is a diagram illustrating a pcDNA 3.1 plasmid, which is a plasmid containing a nucleic acid sequence encoding Cas 9 or a variant thereof.

2 is a diagram schematically schematically illustrating a vector map of a mutant of the spCas9 gene editor protein (HypaCas9, SpCas9-HP1, evoCas9 and eSpCas9(1.1)) used in Examples.

3A is a diagram showing a plasmid including a guide RNA used in the experiment, and FIG. 3B is a diagram showing a vector map when the spCas9 gene editor protein and guide RNA are converted into an All-in-One vector system (in this case) It is constructed by inserting the U6 promoter-guide RNA-scaffold sequence portion of FIG. 3A in front of the CMV/EF-1α promoter of the Cas9 plasmid).

4 is a diagram illustrating HEK293T cells by transfection with a plasmid encoding TRAC guide RNA, and confirming the expression level through enhanced Green Fluorescent Protein (eGFP) fluorescence.

5 is a view showing the main pattern, confirming the gene editing with TRAC guide 1 (SEQ ID NO: 1) and the guide RNA and SpCas9-HF1, evoCas9-HF1, eSpCas9 and HypaCas9 confirmed to have high indel efficiency.

6 is a view showing the main pattern, confirming the gene editing pattern of TRAC guide 2 (SEQ ID NO: 2) and the guide RNA and SpCas9-HF1, evoCas9-HF1, eSpCas9 and HypaCas9 confirmed to have high indel efficiency.

7 is a view confirming the gene editing pattern of TRAC guide 3 (SEQ ID NO: 3) and the guide RNA and SpCas9-HF1 and evoCas9-HF1 confirmed to have high indel efficiency.

8 is a diagram confirming the gene editing pattern of TRAC guide 4 (SEQ ID NO: 4) and the guide RNA and eSpCas9 and HypaCas9 confirmed to have high indel efficiency.

Hereinafter, an aspect will be described in more detail through Examples and Experimental Examples. However, these Examples and Experimental Examples are for illustratively describing an aspect, and the scope of an aspect is not limited to these Examples and Experimental Examples, and the Examples and Experimental Examples of an aspect are average knowledge in the art. It is provided to more completely explain an aspect to those with

Example 1: High-fidelity CRISPR/Cas9 plasmid cloning

HypaCas9, SpCas9-HP1, evoCas9, and eSpCas9(1.1) (HypaCas9, SpCas9-HP1, evoCas9, eSpCas9(1.1) (Professor Hyung-Beom Kim's laboratory, Yonsei University College of Medicine) were cloned into pcDNA 3.1 vector (Thermofisher) with improved accuracy. The high-fidelity Cas9 variant interacts with the DNA-RNA heteroduplex to modify the REC3 domain that binds to the target site, or cuts the HNH domain that cuts the complementary DNA strand or the non-complementary DNA strand. We used a Cas9 variant that reduced the probability of off-target effect while maintaining on-target efficiency by modifying the RuvC III domain that generates DNA double-strand breaks (DSBs).

In order to quickly check the efficiency of guide RNA in HEK293T, the CMV promoter was used. CMV is the most widely used promoter and shows strong expression in most cell lines, and CMV is basically configured in pcDNA3.1 plasmid. As a promoter, the CMV promoter or EF- operably linked to the Cas9 mutant The 1α promoter was used. In addition, since IRES is more stable than P2A, the vector was constructed to be expressed in the form of Cas9-IRES-eGFP by utilizing the IRES sequence between Cas9 and EGFP. A schematic diagram of the specifically used IRES-eGFP expression vector is shown in FIG. 1, and vector maps of four Cas9 variants HypaCas9, SpCas9-HP1, evoCas9, and eSpCas9(1.1) are shown in FIG. 2, respectively.

Example 2: Guide RNA plasmid cloning

2-1: Guide RNA design

Four guide RNAs targeting the TRAC gene were synthesized. A guide RNA capable of knocking out TRAC in exon 1 of the human TRAC gene was designed. The positions and sequences of the four guide RNA candidate sequences are shown in Table 1 below.

TRAC	location	Target candidate sequence (5'-3')	SEQ ID NO:
Guide1	19:48	AGAGTCTCTCAGCTGGTACA	One
Guide2	08:37	GCTGGTACACGGCAGGGTCA	2
Guide3	02:31	ACACGGCAGGGTCAGGGTTC	3
Guide4	139:168	TGTGCTAGACATGAGGTCTA	4

2-2: Guide RNA plasmid cloning

GX19 vector was used as a plasmid expressing the guide RNA designed in Example 2-1. The U6 promoter was used as the promoter, and a guide RNA scaffold sequence binding to Cas9 was inserted, and a guide RNA target sequence of 20 bp in size was positioned between the U6 promoter and the scaffold sequence. The oligonucleotide sequences of Table 1 were synthesized, respectively, and annealed using forward/reverse primers, T4 polynucleotide kinase, and NEB annealing buffer. Annealing conditions were set at 95° C. for 5 minutes, followed by ramping to 25° C. (0.1° C. per second). The annealed oligonucleotides were ligated to the GX19 vector digested with BsaI restriction enzyme using T4 ligase. This guide RNA plasmid is shown in FIG. 3A, and a schematic plasmid vector map is shown in FIG. 3B.

Example 3: Transduction of TRAC guide RNA into cells

An experiment was performed to measure the efficiency of the designed guide RNA. HEK293T cells, a human embryonic kidney cell line, were transfected with a plasmid encoding TRAC guide RNA, and the expression level was confirmed by eGFP (enhanced Green Fluorescent Protein) fluorescence. Specifically, Cas9 plasmid 3μg, guide RNA plasmid 1μg (Cas9 to guide ratio is 3:1) in 5 x 10 ⁶ HEK293T cells under the conditions of 1300 v, 20 ms, and 1 pulse using the Neon transfection system (Thermofisher). And 400ng of puromycin plasmid for selecting only the transfected HEK293T cells was added to transfect HEK293T cells. In order to measure the transfection efficiency, the level of eGFP expression was confirmed 5 days after the transfection and shown in FIG. 4 , and then the transfected cells were selected.

As confirmed in FIG. 4 , it was confirmed that HEK293T cells expressed the TRAC guide RNA and high-fidelity Cas9 mutant designed in Examples 1 and 2-1, and the transfected cells were selected.

Example 4: Measurement of indel frequency and selection of optimal guide RNA

Next generation sequencing (NGS) was performed to confirm the optimal guide RNA and the Cas9 variant used. Specifically, next-generation sequencing was performed to measure the frequency of indels (insertion/deletion, indel) in the genome in the cells prepared in Example 3. The indel frequency was calculated according to the following equation.

[Equation 1]

Specifically, NGS prepared and used the primers as follows to enable sequencing of 50-100 bp downstream of the PAM (-NGG) sequence of the guide RNA target sequence, a total of 200-250 bp.

Adapter sequence: (5'-3')

Forward 5'-CTACACGACGCTCTTCCGATCT (SEQ ID NO: 5)

Reverse 5'-GTGACTGGAGTTCAGACGTGTGCTCTTCCGATCT (SEQ ID NO: 6)

Specifically, the NGS result was analyzed using the web-based NSG analyzer algorithm afterwards, and the NGS result was input to compare the insertion and deletion ratios, size, and sequence information, and the mutation rate due to indels in all cells was confirmed. did.

Experiments were conducted with a total of 5 guide RNAs and 4 types of Cas9 variants (eSpCas9, evoCas9, HypaCas9, SpCas9-HF1). Table 2 shows the results of checking indel frequency using is shown in Table 5.

evoCas9	score	Indel freq (%)
Guide 1	Top 1	40.33
Guide 2	Top 2	40.00
Guide 3	Top 3	20.65

HypaCas9	score	Indel freq (%)
Guide 1	Top 1	74.36
Guide 2	Top 2	62.57
Guide 4	Top 3	44.95

SpCas9-HF1	score	Indel freq (%)
Guide 1	Top 1	69.73
Guide 2	Top 2	56.74
Guide 3	Top 3	50.12

eSpCas9	score	Indel freq (%)
Guide 1	Top 1	73.71
Guide 2	Top 2	66.33
Guide 4	Top 3	57.74

As shown in Tables 2 to 5, the TRAC guide RNA showing the highest indel efficiency among guide RNAs was TRAC guide 1 (SEQ ID NO: 1) in all of the Cas9 variants SpCas9-HF1, evoCas9, eSpCas9 and HypaCas9, followed by TRAC guide 2 (SEQ ID NO: 2) was confirmed.

Example 5: Confirmation of gene editing efficiency and gene editing pattern through the selected guide RNA

An experiment was performed by the method of Example 4 to check the gene editing efficiency of the guide RNA for TRAC and whether there is a main editing pattern thereof when gene editing occurs. Specifically, an experiment was performed to confirm the gene editing efficiency of four types of guide RNAs for TRAC and their gene editing patterns.

By analyzing the indel frequencies between the Cas9 mutant, evoCas9, HypaCas9, SpCas9-HF1 and eSpCas9 and guide RNA, respectively, the indel frequencies of the three guides with the highest indel frequency were identified, and the results are shown in Tables 6 to 9 in turn. It was.

evoCas9	score	Indel freq (%)
Guide 1	Top 1	40.6
Guide 2	Top 2	38.7
Guide 3	Top 3	0.2

HypaCas9	score	Indel freq (%)
Guide 1	Top 1	69.7
Guide 2	Top 2	55.0
Guide 4	Top 3	49.8

SpCas9-HF1	score	Indel freq (%)
Guide 1	Top 1	74.3
Guide 2	Top 2	60.6
Guide 3	Top 3	0.6

eSpCas9	score	Indel freq (%)
Guide 1	Top 1	73.4
Guide 2	Top 2	64.8
Guide 4	Top 3	57.4

In addition, the pattern showing the most main among the gene editing identified with the guide RNA was confirmed, and the results of the confirmation are shown in Tables 10 and 11, respectively, of evoCas9 and HypaCas9 Cas9 mutants, and SpCas9-HF1 and eSpCas9 are sequentially shown in Table 12 to Table 13.

evoCas9	Of total indel freq (%)	Of total in/del freq (%)
Guide 1	31	78
Guide 2	66	67
Guide 3	63	63

HypaCas9	Of total indel freq (%)	Of total in/del freq (%)
Guide 1	31	78
Guide 2	58	62
Guide 4	25	74

SpCas9-HF1	Of total indel freq (%)	Of total in/del freq (%)
Guide 1	28	79
Guide 2	60	63
Guide 3	79	79

eSpCas9	Of total indel freq (%)	Of total in/del freq (%)
Guide 1	28	78
Guide 2	58	61
Guide 4	17	71

An experiment was performed to confirm the gene editing pattern of TRAC guides 1 to 4. First, the gene editing patterns of evoCas9, HypaCas9, SpCas9-HF1 and eSpCas9, which were confirmed to have high indel efficiency with TRAC guide No. 1 and the guide RNA, were checked, and the results confirmed as the main pattern are shown in FIG. 5 . As confirmed, numerically, there were many deletions, but the 1bp insertion frequency was the highest as the main pattern, and in the case of TRAC guide 1, regardless of the type of Cas9 mutant, AACTCTAACCAGCTG showed the most A 1bp insertion pattern between the CCGTGTACCAGCTG sequences. Confirmed.

Thereafter, the gene editing patterns of SpCas9-HF1, evoCas9-HF1, eSpCas9, and HypaCas9, which were confirmed to have high indel efficiency with TRAC guide 2 and the guide RNA, were confirmed, and the results confirmed as the main pattern are shown in FIG. 6 .

As confirmed in FIG. 6 , it was confirmed that guide 2 had a large number of deletions as the main pattern, and in particular, it was confirmed that the 6bp deletion pattern of ACCCTG appeared the most in the CAGAACCCTGACCCT sequence.

Thereafter, the gene editing patterns of TRAC guide 3 and the guide RNA and SpCas9-HF1 and evoCas9-HF1, which were confirmed to have high indel efficiency, were confirmed, and the confirmed results are shown in FIG. 7 .

As confirmed in FIG. 7 , it was confirmed that guide 3 had many numerical deletions, and in particular, it was confirmed that the CCCTGACCCTG 11bp deletion pattern appeared most in the AACCCTGACCCTGCC sequence.

Thereafter, the gene editing patterns of TRAC guide 4 and the guide RNA and eSpCas9 and HypaCas9 confirmed to have high indel efficiency were confirmed, and the confirmed results are shown in FIG. 8 .

As confirmed in FIG. 8 , it was confirmed that guide 4 had many numerical deletions, but the most major editing pattern was ATGAGGTCTATGGA between the ATGAGGTCTATGGA sequences, and it was confirmed that the T 1bp insertion pattern was the most frequent.

In summary, as confirmed in Tables 10 to 13, it was confirmed through NGS result analysis that TRAC guide 1 showed the highest ratio of main patterns in total indel frequency, and main insertion of TRAC guide 2 in total insertion frequency. It was confirmed that the pattern appeared the highest. As a result of checking the main pattern, TRAC guide 1 had A insertion and guide 2 had the most ACCCTG 6bp deletion, guide 1 had the highest total insertion frequency, and guide 2 showed a higher ratio of main pattern to total indel frequency. confirmed that. In general, the gene editing efficiency of Guide 1 was high, but it was confirmed that Guide 2 also exhibited sufficiently excellent editing ability when considering the mail pattern.

In the case of TRAC guide RNA, it was confirmed that TRAC guide 1 exhibited the highest indel frequency in combination with all Cas9 variants evoCas9, SpCas9-HF1, HypaCas9, and eSpCas9 (1.1), followed by guide 2 with the highest indel frequency. It was confirmed that the gene editing efficiency was excellent.

The above description is for illustration, and those of ordinary skill in the art to which the present invention pertains will understand that it can be easily modified into other specific forms without changing the technical spirit or essential features of the present invention. Therefore, it should be understood that the embodiments described above are illustrative in all respects and not restrictive.

Claims (10)

1. A guide RNA comprising a nucleic acid sequence identical to or complementary to one type of polynucleotide selected from the group consisting of SEQ ID NOs: 1 to 4.
2. The guide RNA according to claim 1, wherein the complementary nucleic acid sequence is a polynucleotide in which one selected polynucleotide is transcribed.
3. The guide RNA according to claim 1, wherein the guide RNA hybridizes with the TRAC gene.
4. The guide RNA according to claim 1, wherein the guide RNA is bound to at least one site in the region consisting of exon 1 of the TRAC gene.
5. The guide RNA according to claim 1, wherein the guide RNA induces modifications in the nucleic acid sequence of the TRAC gene.
6. 6. The method of claim 5, wherein the modification in the nucleic acid sequence is

   1) Deletion of the entire or consecutive 1bp to 15bp nucleotide sequence region of the TRAC gene;

   2) substitution of 1 to 15 nucleotides of the TRAC gene with nucleotides different from those of the wild-type gene;

   3) insertion of 1 to 15 nucleotides each independently selected from A, T, C and G into TRAC, or

   4) A combination of two or more selected from 1) to 3) above

   Guide RNA by.
7. a nucleic acid sequence identical to or complementary to one polynucleotide selected from the group consisting of SEQ ID NOs: 1 to 4; and

   Cas9 editor protein or variant thereof; or a CRISPR/Cas9 system comprising a nucleic acid sequence encoding the same.
8. The CRISPR/Cas9 system according to claim 7, wherein the variant of the Cas9 editor protein is at least one selected from the group consisting of HypaCas9, SpCas9, evoCas9, eSpCas9, Sniper-Cas9, SpCas9-HF1 and xCas9.
9. a nucleic acid sequence identical to or complementary to one polynucleotide selected from the group consisting of SEQ ID NOs: 1 to 4; and

   Cas9 editor protein or variant thereof; Or a recombinant vector comprising a nucleic acid sequence encoding the same.
10. a guide RNA and a Cas9 editor protein comprising a nucleic acid sequence identical to or complementary to one polynucleotide selected from the group consisting of SEQ ID NOs: 1 to 4, or a variant thereof; Or a composition for TRAC gene editing comprising a nucleic acid sequence encoding the same.

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