CN108715850B

CN108715850B - GING2 gene knockout in epidermal stem cells by using CRISPR-Cas system

Info

Publication number: CN108715850B
Application number: CN201810570225.9A
Authority: CN
Inventors: 杨骏; 朱成光
Original assignee: Aiyi Life Technology Guangdong Co Ltd
Current assignee: Aiyi Life Technology (Guangdong) Co., Ltd
Priority date: 2018-06-05
Filing date: 2018-06-05
Publication date: 2020-10-23
Anticipated expiration: 2038-06-05
Also published as: CN108715850A

Abstract

The invention provides GINS2 gene editing aiming at epidermal stem cells by adopting a CRISPR-cas system, and particularly relates to establishment of an epidermal stem cell line for constructing GINS2 gene knockout. Two specific gRNAs are constructed and obtained, and the gene editing efficiency of the CRISPR/Cas9 in the epidermal stem cell to GINS2 can be obviously improved. The epidermal stem cell GINS2 knockout plasmid provided by the invention has better genetic stability and higher targeting efficiency.

Description

GING2 gene knockout in epidermal stem cells by using CRISPR-Cas system

Technical Field

The invention provides a method for editing a GING2 gene aiming at an epidermal stem cell by using a CRISPR-cas system, and particularly relates to establishment of an epidermal stem cell line with a GING2 gene knockout structure.

Background

Epidermal stem cells (epistem cells, EpiSCS) are stem cells with the potential for self-proliferation and multidirectional differentiation, the normal proliferation and differentiation of which are essential requirements for maintaining the structural and functional integrity of the skin and its appendages (sweat gland hair, sebaceous glands). Under physiological conditions, the epidermal stem cell is differentiated into a stem cell and a transient amplifying cell (TA cell) by an asymmetric division mode, and the TA cell is differentiated into a Post-mitotic cell (Post-mitotic cell) and a terminal differentiated cell (terminal-differentiated cell) after multiple divisions so as to meet the requirement of continuous renewal of the epidermal cell. Studies have shown that epidermal stem cells not only can be subcultured for long periods in vitro and retain their proliferative differentiation potential (Dunnwald et al, Exp dermaltol, 2001, 10: 45-54.Papini et al stem cells, 2003, 21: 481-: 20: 21-31]. Therefore, the purified epidermal stem cells can be obtained, which not only can provide seed cells for constructing artificial skin with physiological functions, but also can be used for gene therapy and the production of transgenic animals.

Human pluripotent stem cells (hPSCs) and genome editing technology are combined to establish a cell model, and a unique experimental platform is provided for disease research. By utilizing the platform system, researchers can research the influence of specific gene mutation and even chromosome structure variation on various cell types and tissue and organ functions of human beings and detailed molecular mechanisms thereof, and can establish 'personalized' disease models carrying different genetic mutations for large-scale drug screening. The establishment of the model system benefits from the rapid development of a genome editing technology, in particular a CRISPR/Cas9(clustered modular shortpalindromic repeats/CRISPR-associated polypeptides 9, CRISPR/Cas9) technology.

GINS2 is a member of the GINS family of the DNA replication complex, located on human chromosome 16q24, whose mRNA is 1196bp in length and encodes a protein with a relative molecular mass of 21000. GINS is a replication helicase that opens a DNA double strand before moving to the replication fork. It has been shown that members of the GINS family play a role in the development of cancer, e.g., the GINS family is overexpressed in invasive melanoma, and that DNA replication-related proteins play different roles in different cells, e.g., GINS functions in determining the number of centrosome replications and the different stages of disease development, and is particularly closely related to chromosome segregation.

However, there are few reports of GINS2 in tumor-related fields. In CN106620703A, aiming at a small interfering RNA sequence, an RNA interfering vector and an RNA interfering lentivirus of a human GINS2 gene, the silencing efficiency of the GINS2 gene and the influence of the GINS2-siRNA lentivirus on the proliferation capacity and the apoptosis level of tumor cells are further detected, and the result shows that after the expression of the human GINS2 gene is down-regulated by an RNAi method, the proliferation and the growth of the tumor cells can be effectively inhibited and the apoptosis of the tumor cells can be promoted, which indicates that the GINS2 gene is a protooncogene and can be used as a target spot for tumor treatment, and the silencing of the expression of the GINS2 gene by the RNAi method can be used as an effective means for inhibiting the tumor development. However, in this study, SiRNA was used for interference, and the method has the disadvantage that the knockout was not complete and the inheritance could not be stably knocked out. In (Integration of Genomic, biological, and chemical applications to Target p53Loss and Gain-of-Function in Triple reactive Breast cancer), although it is mentioned that CRISPR/Cas can be used in MCM2, GINS2, C19orf43, ELOVL2, ARL4D, DNM3OS, FGFR2, IFIT2, MPPED2, B2M, ERRFI1, GLUL CASP4, CPED1, SPTLC2, CMTM6, CFH, CARS2, SUMF1, it is only one idea and not implemented. CRISPR modification of different genes is not simple and easy to design, and requires overcoming numerous obstacles, with great experimental difficulties.

Based on the pluripotency of epidermal stem cells, in order to study the function of the GINS2 gene-knocked-out epidermal stem cells in cancer treatment, it becomes important to establish GINS2 gene-knocked-out epidermal stem cell lines.

Disclosure of Invention

The invention aims to provide an epidermal stem cell with a GINS2 gene knocked out, which effectively overcomes the technical defect that the prior art uses siRNA for interference and can not stably inherit.

In order to achieve the above object, the present invention provides a target of CRISPR-cas system, and specific sgrnas designed according to the gene sequence of GINS2 are as follows:

GINS2-sgRNA7：5’to 3’aatgcccagcccttactaca

GINS2-sgRNA23：5’to 3’tgcatggaagccatcacact。

to achieve the above objects, the present invention provides a method for increasing CRISPR-cas system to knock out GINS2 gene in epidermal stem cells, comprising introducing into a host cell a potentiating protein, which is a protein encoded by the nucleotide sequence shown in seq id No. 1, ESCS-higher.

Further, the potentiating protein comprises a) or b):

a) 1, and a polynucleotide sequence of a protein coded by the nucleotide sequence shown in SEQ ID NO;

b) the amino acid sequence shown in SEQ ID NO. 2.

Still further, there is provided a system for gene editing using CRISPR/Cas9 in epidermal stem cells, characterized in that the system comprises: (1) for expressing SEQ ID NO:1 the plasmid of ESCS-higher; (2) a PX 330-expressing plasmid (which can express sgRNA and cas9) into which sgRNA has been inserted.

Further, the sgRNA and cas9 expression vectors may also be other expression vectors commonly used in the art.

The invention provides a method for editing GINS2 by using CRISPR/Cas9 gene in epidermal stem cells, which has the following advantages:

the invention provides 2 specific gRNAs which can specifically knock out the GINS2 gene in an epidermal stem cell by designing and optimizing the gRNAs for nearly one hundred times, and the method has a strong knock-out effect.

Drawings

FIG. 1 is a graph showing the result of detecting the expression of GINS2 protein by Western-blot; 4 is epidermal stem cell blank control; 3 represents the effect of gRNA7 into which no potentiating protein was introduced; 2 is the effect of gRNA7 introduced with a potentiated protein; reference numeral 1 denotes the effect of introducing gRNA23 as a potentiated protein.

The technical solution of the present invention is further described in detail by the accompanying drawings and embodiments.

Detailed Description

The technical scheme of the method for improving the genome editing efficiency of the invention is further illustrated by the specific examples.

Example 1 construction of CRISPR expression vectors

Design of gRNA

According to the gene sequence of a target gene, the specific form of sgRNA obtained by the applicant through early optimization design and specific screening from dozens of grnas is as follows:

GINS2-sgRNA7：5’to 3’aatgcccagcccttactaca

GINS2-sgRNA23：5’to 3’tgcatggaagccatcacact。

according to the above gRNA, a forward oligonucleotide sequence was obtained by adding CACC to the 5 'end of the gRNA, a reverse oligonucleotide sequence was obtained by adding AAAC to the 5' end of the complementary strand, and the forward and reverse oligonucleotide sequences were synthesized, respectively, and then the synthesized sequences were denatured and annealed to obtain a double-stranded DNA fragment having a BbsI cohesive end, as follows: forward direction: 5' -CACCNNNNNNNNNNNNNNNNNNNN reverse: NNNNNNNNNNNNNNNNNNNNCAAA-5', the denaturation and annealing system is as follows: mu.l forward oligonucleotide strand (50. mu.M) 2. mu.l reverse oligonucleotide strand (50. mu.M) 46. mu. l l. mu.NEB buffer was run in a PCR instrument following the following procedure: 4min at 90 ℃; 72 ℃ for 10 min; 22min at 37 ℃; 25 ℃ for 25 min.

The annealed double-stranded oligonucleotide chain contains a cohesive end of BbsI, and is directly connected with a pX330-U6-Chimeric _ BB-CBh-hSpCas9 (hereinafter referred to as PX330) vector cut by BbsI, so that a PX330-gRNA-Cas9 recombinant plasmid can be obtained.

Enzyme digestion system: 39.3. mu.l of water, 5. mu.l of 10. mu.l of FD buffer, 2. mu.l of BbsI, and 2. mu.l (2. mu.g) of PX 3303.7. mu.l (2. mu.g) digested plasmid in 37 ℃ water bath for 2h were recovered directly by using a gel recovery kit.

A connection system: annealing product 0.5 μ l, linearized PX330 plasmid 2 μ 1, 5 × ligationbuffer2 μ l, T4DNAligase (3 units/. mu.1), 1 μ l, water 4.5 μ l, water bath 2h at 16 deg.C to transform the ligation product obtained in the above steps into JM109 competent cells, coating on LB plate of Amp +, picking positive clone inoculation, shaking table at 37 deg.C overnight, plasmid extraction kit extracting plasmid and sequencing identification to obtain PX330-gRNA plasmid.

Example 2 cloning of the synergistic protein ESCS-higher and construction of the vector

Cloning the synergistic protein ESCS-higher gene, and obtaining the amino acid sequence shown in SEQ ID NO:1, the gene sequence is used as a template, the sequences of upstream and downstream primers are 5'-atgatatactttattagaat-3' and 5'-tcaagggatttccatttctc-3' respectively, and the primers and the whole genome are synthesized by Shanghai Biotech Co., Ltd. And (2) amplifying the ESCS-higher gene target gene fragment by PCR reaction, wherein the amplification reaction system comprises 95 ℃, 40s, 57 ℃, 1min, 72 ℃, 10min and 35 cycles, PCR products are sequenced by Shanghai's Productivity Co., Ltd, and the PCR products are combined with the sequences shown in SEQ ID NO:1 are perfectly matched. And then, connecting the target gene amplified by the PCR to an empty vector lentiviral vector pHIV-CS-CDF-CG-PRE, and identifying the recombinant lentiviral vector by methods of PCR amplification, enzyme digestion, sequencing and the like. The combination proves that the recombinant lentiviral vector is successfully constructed. The recombinant lentiviral vector plasmids were then co-infected with helper plasmids (ESCs) (isolated and cultured according to the method of claim 1 in CN 1253558C) and packaged by recombination into epidermal stem cells expressing the ESCS-higher gene. Stably transfected stem cells were used for subsequent gene editing applications as identified by PCR screening.

Example 3 analysis of the use of CRISPR/Cas9 in epidermal Stem cells

The sgRNA expression plasmid prepared in example 1, the well-known Cas9 expression plasmid, was co-transfected into epidermal stem cells. Lipofectamine is prepared by transfecting the constructed epidermal stem cell with liposome transfection method and using Lipofectamine as reagent^TM2000 (invitrogen) and the detailed steps of transfection are described in the instructions for transfection. Stem cells not transfected with the enhanced gene of example 2 were used as positive controls.

Example 4Western-blot detection of GINS2 protein expression

1. Total protein extraction

Cultured cell lysis

(1) And (3) removing the adherent cells of the epidermal stem cells, removing the culture solution, washing once with PBS, suspending the cells, centrifugally collecting, and washing once with PBS.

(2) Usually, 0.1ml RIPA buffer is added to every 106 cells, and the lysate is brought into contact with the cells.

(3) The cells were fully lysed by gentle blowing with a pipette tip after a few minutes on ice, and the lysate was then poured onto one side or corner of a petri dish by gentle tilting, then transferred to a 1.5ml centrifuge tube and shaken vigorously for 30 seconds.

(4) Centrifuging at 4 deg.C for 5min at 12,000 Xg, and collecting supernatant for subsequent electrophoresis, Western or immunoprecipitation.

Tissue mass lysis

(1) The tissue is sheared into fine fragments. 1ml of RIPA lysate was added per 100 mg of tissue. Homogenize manually 20 times up and down with a glass homogenizer.

(2) The homogenate was transferred to a 1.5ml centrifuge tube.

(3) Centrifuging at 4 deg.C for 5min at 12,000 Xg, and collecting supernatant for subsequent electrophoresis, Western or immunoprecipitation.

2. Protein concentration determination (BCA protein concentration determination)

Preparation of working fluid

(1) Before the measurement, the mixture was mixed at a ratio of BCA Reagent A to BCA Reagent B of 100:1 to prepare a working solution, and for example, when 30ml of the working solution was prepared, 0.3ml of BCA Reagent B was added to 30ml of BCA Reagent A, and the thus prepared working solution was sufficiently shaken and mixed, and then stored at 4 ℃ for three days.

(2) The required working fluid amount is calculated as follows:

total volume (ml) of working solution required to be [ (8 parts or 7 parts of BSA standard solution + number of samples to be detected) × parallel number of samples (n) +1] × 1 sample

Example) standard procedure [ 1ml reaction system ] when the number of samples tested is 12, replicates (n ═ 2): [ (8+12) × 2+1] × 1ml ═ 41ml

Example) standard procedure [ 200 μ l reaction system ], number of samples tested 20, replicates (n ═ 2): [ (8+20) × 2+1] × 0.2ml ═ 11.4ml

Example) procedure for low concentration protein sample determination [ 1ml reaction system ], number of samples tested 12, parallel sample (n ═ 2): [ (7+12) × 2+1] × 0.5ml ═ 19.5ml

3. Standard operation procedure of low concentration protein sample (quantitative range: 0-200 mug/ml)

[ 0.2ml reaction System, assay Using microwell plates ]

1) And (3) preparing a BSA standard solution.

(1) Preparation of 0.2mg/ml BSA standard solution: mu.l BSA Standard Solution (2mg/ml) was added to 1,080. mu.l of the dilution and mixed well.

(2) The BSA standard solution was diluted at different concentrations, and deionized water, 0.9% NaCl, or PBS was used for dilution of the BSA standard solution and the test sample.

2) Preparation of BSA Standard Curve

(1) 100. mu.l of the diluted BSA standard solutions were added to the plate, and 2 replicates were taken at each concentration.

(2) After 100ul of working solution was added, the mixture was immediately mixed.

(3) After reacting in a 37 ℃ water bath for 60 minutes, the mixture was cooled to room temperature.

(4) The absorbance value at 562nm was measured using a spectrophotometer. For the measurement, a 1mL cuvette was used and the water was used for zero calibration. All samples were tested as soon as possible within 20 minutes.

(5) The absorbance value of the BSA standard solution at each concentration was subtracted by the average value of the Blank values, and a standard curve of the BSA standard solution was plotted.

3) Determination of test sample

When the sample is detected, the sample is recommended to be detected simultaneously with the BSA standard solution.

(1) 100 mul of each sample was added to the microplate and 2 replicates of each sample were tested.

(if necessary, measurement can be made after diluting the test sample by the same dilution method as that for the BSA standard solution)

(2) After adding 100. mu.l of the working solution, mix well immediately.

(3) After reacting in a water bath at 37 ℃ for 60 minutes, the reaction mixture was cooled to room temperature.

(4) The microplate reader wavelength was set at 562nm for the determination. Zero calibration with water. All samples were tested as soon as possible within 20 minutes.

(5) The absorbance value of each sample solution was subtracted by the average value of Blank values, and the protein concentration of the test sample was calculated from the standard curve.

SDS-PAGE electrophoresis

(1) The glass plates are aligned and then placed into a clamp for clamping. The card is then vertically mounted on a rack ready for potting.

(2) Preparing 10% separation gel, adding TEMED, immediately shaking up, and filling gel.

(3) When there is a line of refraction between the water and the gel, the gel is said to have solidified. Waiting for 3min for the glue to solidify sufficiently, pouring off the water on the upper layer of the glue, and sucking the water with absorbent paper.

(4) 4 percent of concentrated glue is prepared, and the concentrated glue is immediately shaken up after TEMED is added, so that glue can be filled. The remaining space was filled with the gel concentrate and a comb was then inserted into the gel concentrate.

(5) The concentrated gel was washed with water and placed in an electrophoresis tank. (small glass plate face is inward, big glass plate face is outward if only run a piece of glue, the another side of that groove will be filled with a plastic board and the face that has the word is outward.) (6) take out the sample loading sample and 5 x SDS buffer solution of sample loading according to 4: mixing at a ratio of 1, mixing, and decocting in boiling water for 5min to denature protein.

(7) Adding sufficient electrophoresis solution, and loading the same amount of protein.

(8) And (4) electrophoresis, wherein after 80V runs through the concentrated gel, the voltage is converted to 120V, and when bromophenol blue runs to the bottom of the gel plate, the bromophenol blue just does not run out.

(9) Opening the clamp to keep the black side horizontal, and sequentially filling a sponge pad, filter paper, glue, a PVDF membrane (activated by methanol), the filter paper and the sponge pad on the clamp; and simultaneously, the electrophoretic solution is changed into transfer solution.

(10) The current was regulated to a constant current of 200mA for about 1 hour of transfer.

(11) The membrane was removed and front and back labeled, washed in TBST for 1 minute, and then blocked with blocking solution.

(12) Diluting the corresponding primary antibody to a certain concentration (1:500) by using a confining liquid, wherein the final dilution concentration of the internal reference primary antibody is 1:3000, then incubated for 1.5 hours or overnight at 4 ℃.

(13) The washing was performed 3 times for 5 minutes each with TBST.

(14) The secondary antibody was diluted to a certain concentration (1:3000) with blocking solution and then incubated for 1.5 hours.

(15) Wash 4 times 5 minutes each with TBST.

5. Chemiluminescence, development, and fixation

(1) The reagents A and B were mixed in equal volumes in a test tube and then applied to the front of the PVDF membrane and incubated for approximately 2 minutes.

(2) And (4) entering a dark room, covering a layer of preservative film on the PVDF film, and wiping off the redundant luminous agent. The film is pressed on the preservative film, and different exposure time is selected according to the intensity of the light emission.

(3) And (3) putting the film into a developing solution, immediately putting the film into a fixing solution after a strip appears, washing the film with running water, and drying the film.

(4) The film was scanned and the grey values of the bands of interest were analyzed using the UVP gel image processing system labworks4.6 software.

(5) Detecting the expression of the GINS2 protein in the transfected epidermal stem cells by Western-blot, wherein the result is shown in figure 1, and the expression of the protein is not influenced by the blank control of the epidermal stem cells; the gRNA1 without the introduced synergistic protein can knock out a target gene, and the protein expression has certain influence; the gRNA7 introduced with the synergistic protein has the obvious effect of improving the gene knockout effect and the protein inhibition rate reaches 92.1 percent; the protein expression inhibition rate of the gRNA23 introduced with the synergistic protein reaches 91.0%, and the effect is extremely obvious. Has excellent application prospect and application value.

Finally, it should be noted that the above embodiments are only for illustrating the technical solutions of the present invention and not for limiting, and although the present invention is described in detail with reference to the preferred embodiments, it should be understood by those skilled in the art that modifications or equivalent substitutions may be made on the technical solutions of the present invention without departing from the spirit and scope of the technical solutions of the present invention.

Sequence listing

<110> Luoyang Xuan Zhi Biotech Co., Ltd

<120> GING2 gene knockout in epidermal stem cells by using CRISPR-Cas system

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gtttgttggc ggaagcgtgt aaaatcagag tacatgcgac tgagacagct caagaggttc 120

agacgagctg atgaagtaaa gagtatgttt agttccaatc gtcagaaaat tttggaaaga 180

acggaaatct taaaccaaga atggaaacag cgaaggatac agcctgtgca catcctgact 240

tctgtgagct cattgcgcgg gactagggag tgttcggtga ccagtgactt ggattttcca 300

acacaagtca tcccattaaa gactctgaat gcagttgctt cagtacccat aatgtattct 360

tggtctcccc tacagcagaa ttttatggtg gaagatgaaa ctgttttaca taacattcct 420

tatatgggag atgaagtttt agatcaggat ggtactttca ttgaagaact aataaaaaat 480

tatgatggga aagtacacgg ggatagagaa tgtgggttta taaatgatga aatttttgtg 540

gagttggtga atgcccttgg tcaatataat gatgatgacg atgatgatga tggagacgat 600

cctgaagaaa gagaagaaaa gcagaaagat ctggaggatc accgagatga taaagaaagc 660

cgcccacctc ggaaatttcc ttctgataaa atttttgaag ccatttcctc aatgtttcca 720

gataagggca cagcagaaga actaaaggaa aaatataaag aactcaccga acagcagctc 780

ccaggcgcac ttcctcctga atgtaccccc aacatagatg gaccaaatgc taaatctgtt 840

cagagagagc aaagcttaca ctcctttcat acgcttttct gtaggcgatg ttttaaatat 900

gactgcttcc tacatcgtaa gtgcaattat tcttttcatg caacacccaa cacttataag 960

cggaagaaca cagaaacagc tctagacaac aaaccttgtg gaccacagtg ttaccagcat 1020

ttggagggag caaaggagtt tgctgctgct ctcaccgctg agcggataaa gaccccacca 1080

aaacgtccag gaggccgcag aagaggacgg cttcccaata acagtagcag gcccagcacc 1140

cccaccatta atgtgctgga atcaaaggat acagacagtg atagggaagc agggactgaa 1200

acggggggag agaacaatga taaagaagaa gaagagaaga aagatgaaac ttcgagctcc 1260

tctgaagcaa attctcggtg tcaaacacca ataaagatga agccaaatat tgaacctcct 1320

gagaatgtgg agtggagtgg tgctgaagcc tcaatgttta gagtcctcat tggcacttac 1380

tatgacaatt tctgtgccat tgctaggtta attgggacca aaacatgtag acaggtgtat 1440

gagtttagag tcaaagaatc tagcatcata gctccagctc ccgctgagga tgtggatact 1500

cctccaagga aaaagaagag gaaacaccgg ttgtgggctg cacactgcag aaagatacag 1560

ctgaaaaagg acggctcctc taaccatgtt tacaactatc aaccctgtga tcatccacgg 1620

cagccttgtg acagttcgtg cccttgtgtg atagcacaaa atttttgtga aaagttttgt 1680

caatgtagtt cagagtgtca aaaccgcttt ccgggatgcc gctgcaaagc acagtgcaac 1740

accaagcagt gcccgtgcta cctggctgtc cgagagtgtg accctgacct ctgtcttact 1800

tgtggagccg ctgaccattg ggacagtaaa aatgtgtcct gcaagaactg cagtattcag 1860

cggggctcca aaaagcatct attgctggca ccatctgacg tggcaggctg ggggattttt 1920

atcaaagatc ctgtgcagaa aaatgaattc atctcagaat actgtggaga gattatttct 1980

caagatgaag ctgacagaag agggaaagtg tatgataaat acatgtgcag ctttctgttc 2040

aacttgaaca atgattttgt ggtggatgca acccgcaagg gtaacaaaat tcgttttgca 2100

aatcattcgg taaatccaaa ctgctatgca aaagttatga tggttaacgg tgatcacagg 2160

ataggtattt ttgccaagag agccatccag actggcgaag agctgttttt tgattacaga 2220

tacagccagg ctgatgccct gaagtatgtc ggcatcgaaa gagaaatgga aatcccttga 2280

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Asp Gly Pro Asn Ala Lys Ser Val Gln Arg Glu Gln Ser Leu His Ser

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Phe His Thr Leu Phe Cys Arg Arg Cys Phe Lys Tyr Asp Cys Phe Leu

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His Arg Lys Cys Asn Tyr Ser Phe His Ala Thr Pro Asn Thr Tyr Lys

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Arg Lys Asn Thr Glu Thr Ala Leu Asp Asn Lys Pro Cys Gly Pro Gln

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Cys Tyr Gln His Leu Glu Gly Ala Lys Glu Phe Ala Ala Ala Leu Thr

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Ile Lys Asp Pro Val Gln Lys Asn Glu Phe Ile Ser Glu Tyr Cys Gly

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Glu Ile Ile Ser Gln Asp Glu Ala Asp Arg Arg Gly Lys Val Tyr Asp

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AspAla Thr Arg Lys Gly Asn Lys Ile Arg Phe Ala Asn His Ser Val

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Asn Pro Asn Cys Tyr Ala Lys Val Met Met Val Asn Gly Asp His Arg

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Ile Gly Ile Phe Ala Lys Arg Ala Ile Gln Thr Gly Glu Glu Leu Phe

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Phe Asp Tyr Arg Tyr Ser Gln Ala Asp Ala Leu Lys Tyr Val Gly Ile

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755

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aatgcccagc ccttactaca 20

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tgcatggaag ccatcacact 20

Claims

1. A CRISPR-CAS system for epidermal stem cell GINS2 gene editing, characterized in that: the system comprises the following components: (1) for expressing SEQ ID NO:1, the plasmid of ESCS-higher; (2) expresses SEQ ID NO: 3 or 4, sgRNA shown and PX330 plasmid of Cas 9.

2. The system of claim 1, wherein: (1) the plasmid (2) is introduced into a gene-editing cell in advance, and after a positive cell is obtained by screening, the plasmid (2) is transferred.

3. Use of the system of claim 1 for the preparation of an agent for epidermal stem cell GINS2 gene editing.