Patent Application
20210002652
The present invention relates to the technical field of gene engineering, specifically to a CRISPR/Cas9 vector and a use thereof in gene knockout.
At present, mechanical artificial heart valves or glutaraldehyde-fixed wild-type heart valves from pig or bovine tissue (referred to as GBHV) are clinically used for cardiac replacement therapy. Although they have been applied clinically, some problems leading to poor transplantation effect still exist. First, glutaraldehyde fixation will inactivate vascular endothelial cells, and damage the transplantation effect; second, the calcification of GBHV will cause structural valve degeneration, and patients have to undergo a further operation, thereby increasing the morbidity and mortality; third, studies have shown that 90% of people over 65 maintain a GBHV transplantation success for more than 10 years, while only 18% of adolescents maintain a transplantation success for 3 years. A reason causing the significant difference in transplantation results of people at different ages is that young people wear out quickly, have a stronger immune system, and exhibit more obvious reject reaction. A main factor leading to calcification and structural valve degeneration is an antibody-mediated immune reject reaction.
α-1,3-Galactosyltransferase (GGTA1), CMP-N-acetylneuraminic acid hydroxylase (CMAH) and β-1,4-N-acetyl galactosaminyl transferase 2 (β4GalNT2) which are abundantly expressed in porcine organs and tissues are three types of primary antigens causing xenotransplantation immune reject reaction (Estrada, J. L., et al., Evaluation of human and non-human primate antibody binding to pig cells lacking GGTA1/CMAH/beta4GalNT2 genes. Xenotransplantation, 2015. 22(3): p. 194-202).
Invention objects: To address the antibody-mediated immune reject reaction occurred in the existing cardiac replacement therapy, the present invention provides a GGTA1/CMAH/β4GalNT2-CRISPR/Cas9 vector, and a further object of the present invention is to provide a use of the GGTA1/CMAH/β4GalNT2-CRISPR/Cas9 vector in the knockout of GGTA1/CMAH/β4GalNT2 gene.
Technical Solutions: An SgRNA combination of the present invention, comprising an SgRNA specifically targeting a GGTA1 gene, an SgRNA specifically targeting a CMAH gene and an SgRNA specifically targeting a β4GalNT2 gene, wherein said SgRNA specifically targeting a GGTA1 gene comprising a nucleotide sequence as set forth in SEQ ID No:1, said SgRNA specifically targeting a CMAH gene comprising a nucleotide sequence as set forth in SEQ ID No:2, and said SgRNA specifically targeting a β4GalNT2 gene comprising a nucleotide sequence as set forth in SEQ ID No:3.
A further object of the present invention is to provide a CRISPR/Cas9 vector combination comprising a GGTA1-CRISPR/Cas9 vector, a CMAH-CRISPR/Cas9 vector and a β4GalNT2-CRISPR/Cas9 vector; wherein said GGTA1-CRISPR/Cas9 vector comprising a nucleotide sequence as set forth in SEQ ID No:1, said CMAH-CRISPR/Cas9 vector comprising a nucleotide sequence as set forth in SEQ ID No:2, and said β4GalNT2-CRISPR/Cas9 vector comprising a nucleotide sequence as set forth in SEQ ID No:3.
Said GGTA1-CRISPR/Cas9 vector has a nucleotide sequence as represented by SEQ ID No:4; said CMAH-CRISPR/Cas9 vector has a nucleotide sequence as represented by SEQ ID No:5; and said β4GalNT2-CRISPR/Cas9 vector has a nucleotide sequence as represented by SEQ ID No:6.
Said CRISPR/Cas9 vector is constructed through the following method:
(1) digesting a pX330 plasmid with a restriction enzyme, isolating the digested plasmid with an agarose gel, followed by purifying and recovering the digested product with a gel extraction kit;
(2) annealing the SgRNA sequence in accordance with the following procedures: 37° C. 30 min 95° C. 5 min, and then cooling to 25° C. at a rate of 5° C./min;
(3) linking the digested product obtained in step (1) to the SgRNA sequence annealed in step (2) with a ligase;
(4) treating the system obtained in step (3) with a plasmid-safe exonuclease to remove the improperly linked plasmid;
(5) transforming the plasmid into a competent cell for culture; and
(6) extracting the plasmid from the competent cell cultured in step (5) for sequencing, thereby determining successful construction of the vector.
When said CRISPR/Cas9 vector is a GGTA1-CRISPR/Cas9 vector, said SgRNA nucleotide sequence in step (2) is set forth in SEQ ID No:1; when said CRISPR/Cas9 vector is a CMAH-CRISPR/Cas9, said SgRNA nucleotide sequence in step (2) is set forth in SEQ ID No:2; and when said CRISPR/Cas9 vector is a β4GalNT2-CRISPR/Cas9 vector, said SgRNA nucleotide sequence in step (2) is set forth inSEQ ID No:3.
A further object of the present invention is to provide a use of said CRISPR/Cas9 vector combination in knockout of GGTA1 gene, CMAH gene and β4GalNT2 gene,comprising the following steps:
(1) transforming the CRISPR/Cas9 vector combination into a porcine fetal fibroblast; and
(2) performing a resistance screening on the fibroblast obtained in step (1) with G418 antibiotics, followed by subjecting the fibroblast having resistance to PCR amplification gene sequencing, thereby obtaining the fibroblasts with the GGTA1 gene, CMAH gene and β4GalNT2 gene knocked out.
A further object of the present invention is to provide a use of said CRISPR/Cas9 vector combination in preparation of the heart valve of a pig with the GGTA1 gene, CMAH gene and β4GalNT2 gene knocked out, comprising the following steps:
(1) transforming the CRISPR/Cas9 vector combination into a porcine fetal fibroblast;
(2) performing a resistance screening on the fibroblast obtained in step (1) with G418 antibiotics, followed by subjecting the fibroblast having resistance to PCR amplification gene sequencing, thereby obtaining the fibroblasts with the GGTA1 gene, CMAH gene and β4GalNT2 gene knocked out;
(3) transplanting the nucleus of the fibroblast obtained in step (2) into an enucleated porcine oocytes for culturing to blastocyst stage;
(4) transplanting the blastocyst obtained in step (3) into a surrogate porcine for feeding and parturition; and
(5) extracting the genome of the porcine obtained in step (4), followed by amplification with a PCR primer for genotype identification.
A further object of the present invention is to provide a use of said sgRNA combination in preparation of a kit for GGTA1 gene, CMAH gene and β4GalNT2 gene knockout.
Beneficial effects: (1) By designing an SgRNA sequence including specifically targeting GGTA1 gene, CMAH gene and targeting β4GalNT2 gene, the knockout effects of the three genes are 56%, 63% and 41%, respectively;
(2) by modifying the gene of porcine, knocking out three genes (GGTA1/CMAH/β4GalNT2) associated with the immune reject reaction in a manner of frameshift mutation, it can completely knock out the aforesaid three genes, obtain three-knockout porcine and obtain its heart valve; and
(3) the heart valve of three-knockout porcine exhibits a significantly decreased binding with immunoglobulin in human serum, and produces a significant effect on overcoming a hyperacute immune reject reaction, and effectively solves the problems of xenotransplanted organ shortage and calcification, as well as structural valve degeneration. It has become a source of new materials for GBHV, laid the foundation for gene modification of xenotransplanted organ donors, and provided a valuable source of material for clinical cardiac replacement therapy.
First, an SgRNA (single guide RNA) targeting GGTA1, CMAH and β4GalNT2 gene was synthesized in accordance with the DNA sequence of GGTA1/CMAH/β4GalNT2 gene, and a GGTA1-CRISPR/Cas9 vector, a CMAH-CRISPR/Cas9 vector and a β4GalNT2-CRISPR/Cas9 vector were respectively constructed by use of pX330 as a skeleton plasmid.
I. The GGTA1-CRISPR/Cas9 vector was constructed through the following method:
First, in accordance with the porcine GGTA1 gene sequence disclosed by Genbank, the exon3 of the GGTA1 gene was selected as the CRISPR/Cas9 target. In accordance with the design principles of cas9 target: the 5′ end was G, the 3′end was a PAM sequence (NGG), the SgRNA sequence was designed as GAAAATAATGAATGTCAA, as shown in
The GGTA1 -CRISPR/Cas9 vector was constructed through the following method:
Step (1), in accordance with the design principles of cas9 target that the 5′ end was G and the 3′end was a PAM sequence (NGG), finding the targeting site in the GGTA1 gene;
Step (2), purchasing a pX330 skeleton plasmid expressing hSpCas9 and gRNA (Addgene plasmid 423230); and
Step (3), synthesizing the 5′-end phosphorylated oligonucleotide chain SgRNA sequence GAAAATAATGAATGTCAA by the company.
The SgRNA sequence was cloned into the pX330 skeleton vector in the following specific steps:
1. Digesting lug of pX330 plasmid with a restriction enzyme BbsI;
2. Isolating the digested pX330 plasmid by an agarose gel (an agarose gel at a concentration of 1%, i.e., 1 g of agarose gel was added into 100 mL of electrophoresis buffer), followed by purifying and recovering the digested product with a gel extraction kit (QIAGEN);
3. Annealing the synthesized 5′end phosphorylated oligonucleotide chain SgRNA sequence in accordance with the following procedures:
37° C. 30 min
95° C. 5 min, and then cooling to 25° C. at a rate of 5° C./min.
4. Initiating a linking reaction in accordance with the following system: Reaction at room temperature for 10 min
The BbsI-digested pX330 obtained in step 2 50 ng
The annealed 5′end phosphorylated oligonucleotide obtained in step 3 (1:250 v/v, diluted with sterile water) 1 μL
2× flashlinking buffer (NEB) 5 μL
Diluting the system to 10 μL with ddH2O
Sub-total 10 μL
Flash ligase (NEB) 1 μL
Total 11 μL
5. Treating the linking system with a plasmid-safe exonuclease to remove the improperly linked plasmid:
The linking reaction system obtained in step 4 11 μL
10× plasmid-safe buffer (NEB) 1.5 μL
10 mM ATP 1.5 μL
Plasmid-safe exonuclease (NEB) 1 μL
Total 15 μL
Reaction at 37° C. for 30 min
6. Transforming
(1) 50 μL of competent cells (TIANGEN) were placed in an ice bath;
(2) 15 μL of a solution free of improperly linked plasmid obtained in step 5 was added into a centrifuge tube containing competent cells, and then stood in the ice bath for 30 min after uniformly mixed;
(3) The competent cells ice-cooled for 30 min were placed in a water bath at 42° C. for 60-90 s, and then rapidly transferred into the ice bath, allowing the cells to cool for 2-3 min;
(4) 900 μL of sterile LB medium (free of antibiotics) was added into the centrifuge tube, and placed on a 37° C. shaker for shaking culture at 150 rpm for 45 min after uniformly mixed; and
(5) The centrifuge tube was placed in a centrifuge to undergo a centrifugation at 12000 rpm for 5 min, and then 900 μL of supernatant was discarded, and the precipitates of competent cells were re-suspened in the residual 100 μL of supernatant, the re-suspensed competent cells were added onto an LB solid agar medium containing the corresponding antibiotic, uniformly spread with a sterile spreading rod; and the LB solid agar medium coated with the competent cells was incubated by reversion in a 37° C. incubator for 12-16 h.
7. Carefully extracting the plasmid, sequencing by the company, and identifying for the successful construction of the targeting plasmid.
The constructed CRSAPR/Cas9 vector is designated as GGTA1-PX330, with a full nucleotide sequence as set forth in SEQ ID No:4.
II. CMAH-CRISPR/Cas9 Vector was Constructed through the Following Method:
First, in accordance with the porcine CMAH gene sequence disclosed by Genbank, exon6 of the CMAH gene was selected as the CRISPR/Cas9 target. In accordance with the design principles of cas9 target: 5′end was G, 3′end was a PAM sequence (NGG), the SgRNA guide sequence was designed as GAGTAAGGTACGTGATCTGT, as shown in
The CMAH-CRISPR/Cas9 vector was constructed through the following method:
Step (1), in accordance with the design principles of cas9 target that 5′end was G and 3′ end was a PAM sequence (NGG), finding the targeting site in the CMAH gene;
Step (2), purchasing a pX330 skeleton plasmid expressing hSpCas9 and gRNA (Addgene plasmid 423230); and
Step (3), synthesizing the 5′ end phosphorylated oligonucleotide chain SgRNA sequence GAGTAAGGTACGTGATCTGT by the company.
The SgRNA sequence was cloned into the pX330 skeleton vector in the following specific steps:
1. Digesting lug of pX330 plasmid with a restriction enzyme BbsI;
2. Isolating the digested pX330 plasmid by an agarose gel (an agarose gel at a concentration of 1%, i.e., 1 g of an agarose gel was added into a 100 mL electrophoresis buffer), followed by purifying and recovering the digested product with a gel extraction kit (QIAGEN);
3. Annealing the synthesized 5′end phosphorylated oligonucleotide chain SgRNA sequence in accordance with the following procedures:
37° C. 30 min
95° C. 5 min, and then cooling to 25° C. at a rate of 5° C./min.
4. Initiating a linking reaction in accordance with the following system: Reaction at room temperature for 10 min
The BbsI-digested pX330 obtained in step 2 50 ng
The annealed 5′end phosphorylated oligonucleotide obtained in step 3 (1:250 v/v, diluted with sterile water) 1 μL
2× flashlinking buffer (NEB) 5 μL
Diluting the system to 10 μL with ddH2O
Sub-total 10 μL
Flash ligase (NEB) 1 μL
Total 11 μL
5. Treating the linking system with a plasmid-safe exonuclease to remove the improperly linked plasmid:
The linking reaction system obtained in step 4 11 μL
10× plasmid-safe buffer (NEB) 1.5 μL
10 mM ATP 1.5 μL
Plasmid-safe exonuclease (NEB) 1 μL
Total 15 μL
Reaction at 37° C. for 30 min
6. Transforming
(1) 50 μL of competent cells (TIANGEN) were placed in an ice bath;
(2) 15 μL of a solution free of the improperly linked plasmid obtained in step 5 was added to a centrifuge tube containing the competent cells, and stood in the ice bath for 30 min after uniformly mixed;
(3) The competent cells ice-cooled for 30 min were placed in a water bath at 42° C. for 60-90 s, and then rapidly transferred into the ice bath, allowing the cells to cool for 2-3 min;
(4) 900 μL of a sterile LB medium (free of antibiotics) was added into the centrifuge tube, and placed on a 37° C. shaker for shaking culture at 150 rpm for 45 min after uniformly mixed; and
(5) The centrifuge tube was placed in a centrifuge to undergo a centrifugation at 12000 rpm for 5 min, and then 900 μL of supernatant was discarded, and the precipitates of competent cells were re-suspended in the residual 100 uL of supernatant,the re-suspended competent cells were added onto an LB solid agar medium containing the corresponding antibiotic, uniformly spread with a sterile spreading rod; and the LB solid agar medium coated with the competent cells was incubated by reversion in a 37° C. incubator for 12-16 h.
7. Carefully extracting the plasmid, sequencing by the company, and identifying for the successful construction of the targeting plasmid.
The constructed CRSAPR/Cas9 vector was designated as CMAH-PX330, with a full nucleotide sequence as set forth in SEQ ID No:5.
III. β4GalNT2-CRISPR/Cas9 Vector was Constructed through the Following Method:
First, in accordance with the porcine β4GalNT2 gene sequence disclosed by Genbank, exon8 of the β4GalNT2 gene was selected as the CRISPR/Cas9 target. In accordance with the design principles of cas9 target: 5′end was G, 3′end was a PAM sequence (NGG), the guide sequence was designed as GGTAGTACTCACGAACACTC, as shown in
The β4GalNT2-CRISPR/Cas9 vector was constructed through the following method:
Step (1), in accordance with the design principles of cas9 target that 5′end was G and 3′ end was a PAM sequence (NGG), finding the targeting site in the β4GalNT2 gene;
Step (2), purchasing a pX330 skeleton plasmid expressing hSpCas9 and gRNA (Addgene plasmid 423230); and
Step (3), synthesizing the 5′ end phosphorylated oligonucleotide chain SgRNA sequence GGTAGTACTCACGAACACTC by the company.
The SgRNA sequence was cloned into pX330 skeleton vector in the following specific steps:
1. Digesting lug of pX330 plasmid with a restriction enzyme BbsI;
2. Isolating the digested pX330 plasmid by an agarose gel (an agarose gel at a concentration of 1%, i.e., 1 g of an agarose gel was added into a 100 mL electrophoresis buffer), followed by purifying and recovering the digested product with a gel extraction kit (QIAGEN);
3. Annealing the synthesized 5′end phosphorylated oligonucleotide chain SgRNA sequence in accordance with the following procedures:
37° C. 30 min
95° C. 5 min, and then cooling to 25° C. at a rate of 5° C./min.
4. Initiating a linking reaction in accordance with the following system: Reaction at room temperature for 10 min
The BbsI-digested pX330 obtained in step 2 50 ng
The annealed 5′end phosphorylated oligonucleotide obtained in step 3 (1:250 v/v, diluted with sterile water) 1 μL
2× flashlinking buffer (NEB) 5 μL
Diluting the system to 10 μL with ddH2O
Sub-total 10 μL
Flash ligase (NEB) 1 μL
Total 11 μL
5. Treating the linking system with a plasmid-safe exonuclease to remove the improperly linked plasmid:
The linking reaction system obtained in step 4 11 μL
10× plasmid-safe buffer (NEB) 1.5 μL
10 mM ATP 1.5 μL
Plasmid-safe exonuclease (NEB) 1 μL
Total 15 ∞L
Reaction at 37° C. for 30 min
6. Transforming
(1) 50 μL of competent cells (TIANGEN) were placed in an ice bath;
(2) 15 μL of a solution free of the improperly linked plasmid obtained in step 5 was added to a centrifuge tube containing the competent cells, and stood in the ice bath for 30 min after uniformly mixed;
(3) The competent cells ice-cooled for 30 min were placed in a water bath at 42° C. for 60-90 s, and then rapidly transferred into the ice bath, allowing the cells to cool for 2-3 min;
(4) 900 μL of a sterile LB medium (free of antibiotics) was added into the centrifuge tube, and placed on a 37° C. shaker for shaking culture at 150 rpm for 45 min after uniformly mixed; and
(5) The centrifuge tube was placed in a centrifuge to undergo a centrifugation at 12000 rpm for 5 min, and then 900 μL of supernatant was discarded, and the precipitates of competent cells were re-suspended in the residual 100 uL of supernatant, and the re-suspended competent cells were added onto an LB solid agar medium containing the corresponding antibiotic, uniformly spread with a sterile spreading rod, and the LB solid agar medium coated with the competent cells was incubated by reversion in a 37° C. incubator for 12-16 h.
7. Carefully extracting the plasmid, sequencing by the company, and identifying for the successful construction of the targeting plasmid.
The constructed CRSAPR/Cas9 vector was designated as β4GalNT2-PX330, with a full nucleotide sequence as set forth in SEQ ID No:6.
This transgene fragment that can be widely present in mammals and respectively express GGTA1/CMAH/β4GalNT2 genes (see
The constructed GGTA1-CRISPR/Cas9 vector, CMAH-CRISPR/Cas9 vector and β4GalNT2-CRISPR/Cas9 vector, together with tdTomato plasmid were co-transfected into pig fetal fibroblasts. Single cell clones were obtained by G418 screening. GGTA1/CMAH/β4GalNT2 three-knockout pig fetal fibroblasts were obtained by sequencing identification. GGTA1/CMAH/β4GalNT2 three-knockout Landraces were prepared by somatic cell nuclear transfer (SCNT). The genome of the newly born piglet was extracted, amplified by use of a PCR primer, and linked to a T vector for genotype identification.
Step (1), porcine primary fibroblast resuscitation
1. The cryopreserved primary porcine fibroblasts were removed from liquid nitrogen, and thawed in a 37° C. water bath;
2. The thawed cells were transferred into a 15 mL sterile centrifuge tube, and then 3 mL of cell culture medium was added,the mixture was centrifuged at 1500 rpm for 5 min, wherein,
the formula of the complete cell culture medium includes: 16% of fetal bovine serum (Gibco)+84% of DMEM medium (Gibco), in which 16% and 84% are volume percentages.
3. The supernatant was discarded. 2 mL of complete medium was added to re-suspend the cell precipitates, then, the re-suspended cells were spread into a 6-cm cell culture dish, supplemented with 2 mL of complete medium, and placed in a constant temperature incubator at 37° C., 5% CO2 (volume percentage) for culture;
4. When the cells were grown to about 90% of the bottom of the dish, 0.05% (5 g/100 mL) of trypsin was used to digest the cells, and then a complete medium was added to quench the digestion. The cell suspension was transferred to a 15 mL centrifuge tube, centrifuged at 1500 rpm for 5 min, and then the supernatant was discarded,the cells were re-suspended with 2 mL of complete medium,the cells were counted, and the total amount of cells was adjusted to 1.5×106 for use in the next nuclear transfection experiment.
Step (2), Co-transfection of porcine primary fibroblasts with the constructed GGTA1-PX330, CMAH-PX330, β4GalNT2-PX330 and tdTomato plasmid (Clontech, PT4069-5)
The nucleus transfection experiment was carried out by use of Mammalian fibroblast nuclear transfection kit (Lonza) and Lonza Nucleofactor™2b Nucleus Transfector
1. A nucleus transfection reaction solution was formulated. The system was as follows:
Nucleus transfection basic solution 82 μL
Supplementary components 8 μL
2. The three constructed plasmids and the Tdtomato plasmid were added into 100 μL of nucleus transfection reaction solution obtained in step 1 at a mass ratio of 5:1, respectively, and uniformly mixed,be careful not to generate bubbles during the process;
3. The cell suspension prepared in step (1) was washed with 2× Dulbecco's Phosphate Buffered Saline (DPBS) (Gibco), and digested at 37° C. for 2 min. After terminating the digestion with DMEM complete medium containing 10 vol % of fetal bovine serum, the mixture was subject to centrifuge at 1500 rpm for 5 min. The supernatant was discarded, and the cells were re-suspended in the nucleus transfection reaction solution including plasmids obtained in this step 2. During the re-suspension processing, the generation of bubbles should be avoided.
4. The nucleus transfection system was carefully added into an electrotransfection cup provided in the kit, taking care to prevent air bubbles. The electrotransfection cup containing 100 μL of PBS was first placed in the cup slot of the Lonza nucleus transfector. The U023 nucleus transfection program was selected and debugged. Then, the electrotransfection cup containing cells was subject to electro-transfection under electroshock, immediately followed by gently sucking out the liquid in the electrotransfection cup in an ultra-clean table, which was transferred into 1 mL of DMEM complete medium containing 16% fetal bovine serum by volume, and gently mixed to uniform;
5. Several Petri dishes (10 cm) containing 8 mL of complete culture medium were prepared, and the nucleus-transfected cell suspension was pipetted into the Petri dishes containing complete medium, and mixed to uniform. The cells were observed under the microscope for their number, and counted, so that a dish included about 50-60 cells in a field of view under the microscope. Cell suspensions were added to the remaining dishes according to the final amount of this cell suspension, mixed to uniform, and placed in a constant temperature incubator at 37° C., 5% CO2 for culture.
Step (3), Screening of three-knockout cell lines
1. The cells obtained in Step (2) were cultured for 24 h, and then the cell culture medium was replaced with a complete medium containing 1 mg/mL of G418, and placed in a constant temperature incubator at 37° C., 5% CO2 for culture. The cell culture medium was changed every 2-3 days. During this time, the concentration of G418 was gradually decreased in accordance with the cell growth conditions until the final concentration of G418 was 0.3 mg/mL. At Days 10 to 14, monoclonal cell lines having G418 resistance would gradually grow in the culture dish;
2. A cloning ring was used to pick up the cell lines. The picked monoclonal cell lines were seeded into a 24-well plate plated with 0.3 mg/mL G418 complete medium, and placed in a constant temperature incubator at 37° C., 5% CO2 for culture. The cell culture medium was changed every 2-3 days;
3. Once the cells in the 24-well plate covered the bottom of the wells, trypsin was used to digest and collect the cells, wherein ⅘ of the cells were seeded into a 12-well plate or a 6-well plate containing 0.3 mg/mL G418 complete medium (in accordance with cell numbers), and the remaining ⅕ of cells were left in the 24-well plate for further culture;
4. Once the cells in the 12-well plate or the 6-well plate covered the bottom of the wells, 0.05% (5 g/100 mL) of trypsin was used to digest and collect the cells. The cells were frozen for storage with a cell cryopreservation solution (90% fetal bovine serum+10% DMSO, volume ratio);
Step (4), Gene identification of three-knockout cell lines
1. Once the cells in the 24-well plate grew to cover the bottom of the wells, 0.05% (5 g/100 mL) of trypsin was used to digest and collect the cells. Then, 25 ml of NP-40 lysate was added to the cells to lyse the cells to extract the cell genome DNA. The lysis procedure is: 55° C. 60 min −95° C. 5 min −4° C. After the completion of the reaction, the genome DNA was stored at −20° C.;
2. The respective PCR primers were designed against the GGTA1/CMAH/β4GalNT2 gene targeting information, and the PCR primer sequences are respectively:
GGTA1
The PCR target product has a length of 428 bp;
CMAH
The PCR target product has a length of 485 bp;
β4GalNT2
The PCR target product has a length of 399 bp;
3. A PCR reaction was used to amplify the GGTA1/CMAH/β4GalNT2 target gene, and the PCR reaction system is as follows:
Cell genome DNA 2 μL
GGTA1 forward primer (10 pM) 1 μL
GGTA1 reverse primer (10 pM) 1 μL
2× Taq enzyme premix solution 25 μL
dd H2O 21 μL
Total 50 μL
The reaction conditions are as follows:
The amplification of CMAH target gene is the same as the aforesaid steps; and the amplification of β4GalNT2 target gene is the same as the aforesaid steps.
4. The PCR reaction product was subject to an agarose gel electrophoresis (1%, i.e., 1 g of an agarose gel was added into 100 mL of electrophoresis buffer). After the completion of electrophoresis, the target band was cut under ultraviolet light, and then recovered with a gel extraction kit (QIAGEN). The recovered PCR product was tested for concentration by NanoDrop 200;
5. The recovered PCR product was linked to a T vector by a TAKARA pMD™18-T Vector Cloning Kit, and the T vector has the following reaction system:
pMD18-T vector 1 μL
gel-recovered PCR product 81.7 ng*
The system was diluted with ddH2O to 10 uL
*NOTE: In the instructions of the TAKARA pMD™ 18-T Vector Cloning Kit, the dosage of Insert DNA (in this case, the gel-recovered PCR product) in the description is required to be 0.1-0.3 pM. In this case, the dosage is selected as 0.2 pM. The calculation method of dosage is: dosage of Insert DNA (ng)=number of nmol×660×the bp number of Insert DNA.
The reaction conditions of T-vector linking is reacted at 16° C. for 30 min;
6. The T vector linked product obtained in step 5 was transformed with competent cells (TIANGEN). After transformation, the competent cells were plated on an Amp-resistant LB agar solid medium, and incubated at 37° C. in a constant temperature incubator overnight;
10-15 monoclonal colonies were picked from the medium cultured overnight, and sequenced by the sequencing company. The sequencing results were compared with the target GGTA1/CMAH/β4GalNT2 information to determine whether the cell lines were GGTA1/CMAH/β4GalNT2 gene knockout cell lines;
A total of 27 monoclonal cell lines were picked at this time, in which one bi-allelic knockout cell line with three genes knocked out at the same time is available, and the number was 50 #. The status of this clonal genotype is shown in Table 1:
The knockout efficiencies of GGTA1, CMAH, β4GalNT2 gene knockout are 56%, 63% and 41%, respectively.
Comparing the GGTA1/CMAH/β4GalNT2 three-knockout with GGTA1/CMAH two-knockout, the binding to human IgM, IgG is significantly reduced, therefore, the three-knockout is necessary.
Step (5), Somatic cell nuclear transplantation
1. Ovaries of sows over the age of six months were purchased from a slaughterhouse, and immature oocytes were manually extracted from the follicles. Oocytes of better quality were picked under a microscope and placed in a constant temperature incubator of 38.5° C., 5% CO2 for 42-44 h, until oocytes became mature;
2. A microscopic operating system was used to enucleate the mature oocytes in step (1), and then recover the GGTA1/CMAH/β4GalNT2 knockout monoclonal cell lines obtained in step (4). The GGTA1/CMAH/β4GalNT2 knockout cells were injected as a nuclear donor into enucleated oocytes, and each enucleated oocyte was injected with one GGTA1/CMAH/β4GalNT2 knockout cell;
3. The injected cells were activated by an electrofusion technology so that the reconstructed embryos were activated after nuclear transplantation. The embryos were placed in a 38.5° C. incubator for 5 days to develop into morula; and
4. The well-developed embryos were transplanted into the womb of the surrogate sow, which was carefully cared, and detected by B-ultrasound for its pregnancy status one month after transplantation. The surrogate sow was monitored in time until delivery.
Step (6), Genotype analysis of three-knockout Ba-Ma mini pigs
1. After birth, the GGTA1/CMAH/β4GalNT2 gene knockout piglet was cut for its ear tissue, and then a blood/cell/tissue genome DNA extraction kit (TIANGEN) was used to extract the piglet genome DNA;
2. The genome DNA of the piglet obtained in step 1 was subject to a PCR reaction. The PCR reaction conditions are the same as step 4 (3). The PCR reaction product was then sequenced by the sequencing company, and the sequencing results were compared with the GGTA1/CMAH/β4GalNT2 gene target sequence.
At this time, a total of 8 male Landraces were born, numbered as 1-8. The born 8 male piglets had the same results as cell genotype.
Valve extraction process: after perfusion, the piglet was killed and the heart was removed. The envelope outside the heart was peeled off, and then washed with 1× PBS, the fat tissue outside the pericardium was gently peeled off, and then washed with 2× PBS, fixed with 0.2% of glutaraldehyde for at least 48 h for subsequent experiments.
1. Knockout of GGTA1, CMAH and β4GalNT2 genes in WT porcine can effectively decrease the hyperacute immune reject reaction during xenotransplantation.
After weaning, the piglet was subject to blood sampling to isolate peripheral blood mononuclear cells (PBMCs). The piglet was determined by flow cytometry for its gene knockout and its binding to immunoglobulin (IgM, IgG) in human serum. It is found that the three antigens of alpha-1,3-galactosyltransferase (GGTA1), CMP-N-acetylneuraminic acid hydroxylase (CMAH) and β-1,4-N-acetyl galactosaminyl transferase 2 (β4GalNT2) were successfully knocked out in the three-knockout piglets produced by Example 2, as shown in
PBMC is separated by the following method: To 100 μL of anticoagulated blood was added 3 volumes of red blood cell lysate (BD, diluted with 10× deionized water). It was lysed at room temperature for 5 min-10 min. After centrifugation, the supernatant was discarded, and washed with a pre-cold washing solution containing 0.1% FBS (the solvent is PBS, 0.1%, i.e., 0.1 g FBS/100 mL PBS) (enhancing cell sedimentation), rinsed, and centrifuged to obtain PBMC precipitate.
2. Peripheral blood mononuclear cells (PBMCs) were detected by a flow cytometry for the binding level of PBMCs of three-knockout piglets and control wild-type piglets with human immunoglobin. The results show that in comparison with wild-type piglets, the three-knockout porcine exhibits a significant decrease in the binding level of PBMCs to human immunoglobulin, which is close to the level of humans.
FIG.
3. Uniaxial mechanical testing of the pericardium mechanical properties of wild-type and three-knockout pigs
The fresh pericardium of wild-type and three-knockout pigs was fixed with glutaraldehyde for more than 48 h. The pericardium was cut into a dumbbell shape with a length of 14 mm, a width of 2 mm, and a thickness of 2 mm. Each group included 6 samples, with a length of 14.67±1.03 mm, a width of 2.15±0.23 mm, and a thickness of 0.2±0.01 mm. An instron 5943 single column material tensile tester was used to detect the stress and strain of the pericardium. The results showed that the pericardium of three-knockout pig does not exhibit a significant difference of mechanical properties from that of the wild type, as shown in
At present, the clinically used and commercially available glutaraldehyde fixed heart valve has been maturely applied in clinic, but the effect of the heart valve cannot be maintained for a long time due to calcification, immune reject reaction and the like. The heart valves of pigs in which three genes associated with immune reject reaction are knocked out can be used as a source of a new type of biomaterial valve to provide solutions to the problems that arise in clinical cardiac replacement therapy.
| Number | Date | Country | Kind |
|---|---|---|---|
| 201810139547.8 | Feb 2018 | CN | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2019/078060 | 3/14/2019 | WO | 00 |
