COLD-RESISTANT AND LEAN-TYPE TRANSGENIC PIG AND PREPARATION METHOD THEREFOR

Abstract

Disclosed is a cold-resistant and lean-type transgenic pig and a preparation method therefor, which relate to the field of genetic engineering. By transferring a mouse uncoupling protein 1 gene into the genome of a pig, a transgenic pig is obtained which can not only resist the cold but also have an increased lean meat rate by reducing fat deposition. Simultaneous improvement of two important production traits of pigs through the site-directed single gene manipulation not only lays a foundation for the application and basic research of genetic editing for big animals, but also provides with breading researchers a new way of thinking for improving traits of livestock.

Claims

1. A cold-resistant and lean-type transgenic pig, wherein, the pig is a transgenic pig in which UCP1 gene is expressed in adipose tissue.

2. The transgenic pig according to claim 1, wherein, the UCP1 gene is a mouse uncoupling protein 1 gene.

3. The transgenic pig according to claim 1, wherein, the expression of the UCP1 gene is specifically driven by an adiponectin promoter.

4. The transgenic pig according to claim 3, wherein, the adiponectin promoter is a mouse adiponectin promoter.

5. A preparation method of the transgenic pig according to claim 1, wherein, the method comprises the following steps: S1. constructing a donor plasmid comprising a target sequence, an adiponectin promoter and an UCP1 gene; S2. constructing a Cas9/gRNA vector targeting the target sequence; S3. co-transfecting the constructed donor plasmid and the Cas9/gRNA vector into porcine fetal fibroblasts, obtaining monoclonal cells by limiting dilution method, and further obtaining successfully targeted positive cells by PCR genotyping; and S4. using positive colony cells obtained by screening as nuclear transfer donor cells, and isolated oocytes as nuclear transfer recipient cells, and performing somatic cell cloning by nuclear transfer technology to obtain the transgenic pig.

6. The method according to claim 5, wherein, the starting vector of the donor plasmid is a pLB vector.

7. The method according to claim 6, wherein, the nucleotide sequence of the target sequence is represented by SEQ ID NO. 1.

8-10. (canceled)

11. The transgenic pig according to claim 2, wherein, the expression of the UCP1 gene is specifically driven by an adiponectin promoter.

12. The transgenic pig according to claim 11, wherein, the adiponectin promoter is a mouse adiponectin promoter.

13. A method for improving the cold resistance of a transgenic pig, wherein, the method comprises preparing a transgenic pig by the method according to claim 5.

14. A method for increasing the lean meat rate of a transgenic pig, wherein, the method comprises preparing a transgenic pig by the method according to claim 5.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0030] FIG. 1 shows the strategy of the targeting vector construction, and identification of gene knock-in in the present invention.

[0031] FIG. 2 shows the genotyping of positive targeted cells of the present invention.

[0032] FIG. 3 shows genotyping of the transgenic pig of the present invention.

[0033] FIG. 4 is a graph showing changes in the rectal temperature of the pig under the cold condition of the present invention.

[0034] FIG. 5 shows the infrared photograph and body surface temperature of the pig under the cold condition of the present invention.

[0035] FIG. 6 shows measurements of slaughter indexes of the wild-type pig and the transgenic pig of the present invention.

SPECIFIC MODES FOR CARRYING OUT THE EMBODIMENTS

[0036] The preferred embodiments of the present invention will be described in detail below with reference to Examples. It is to be understood that the following Examples are presented for illustrative purposes only and are not intended to limit the scope of the present invention. Various modifications and alterations of the present invention can be made by a person skilled in the art without departing from the purpose and spirit of the present invention.

[0037] The UCP1 expression vector Pcdna3.1 driven by the mouse adiponectin promoter was obtained by cloning the mouse adiponectin promoter and the UCP1 coding sequence into the Pcdna3.1 plasmid backbone. Sequence determination and primer synthesis were performed by Thermo Fisher Co., Ltd. Taq enzyme, T4 DNA ligase and endonuclease were purchased from Beijing NEB Co., Ltd., and the reagents for somatic cell nuclear transfer were purchased from Sigma company. For conventional experimental procedures such as enzyme digestion, ligation, recovery, transformation, and PCR amplification, refer to Molecular Cloning (Third Edition).

[0038] The experimental methods used in the following Examples are conventional methods unless otherwise specified.

[0039] The materials, reagents and the like used in the following Examples are commercially available unless otherwise specified.

Example 1: Preparation of a Transgenic Pig

[0040] The construction of a targeting vector and the knock-in of an exogenous gene were carried out according to the strategy described in FIG. 1.

[0041] 1. Construction of Cas9/gRNA Targeting Vector

[0042] The gRNA recognition sequence was designed using the online tool CRISPR Design Tool (http://crispr.mit.edu/) developed by Professor Zhang Feng of the Massachusetts Institute of Technology and synthesized by Thermo Fisher company, and the gRNA recognition sequence was located in the exon 2 of the pig uncoupling protein 1 pseudogene. The PX330 plasmid containing Cas9 was purchased from Addgene. The PX330 plasmid was first cut with BbsI endonuclease, and the linearized plasmid was purified and recovered. Then, the gRNA recognition sequence was subjected to denaturation and renaturation treatment to change from a single-stranded nucleotide to a double-stranded oligonucleotide, and then the double-stranded DNA was ligated to the linearized PX330 plasmid using T4 DNA ligase. Transformation, spreading the obtained bacteria solution onto a plate and cultivation were performed, followed by further sequencing to identify positive bacterial, and performing large-scale extraction of plasmids for later use.

[0043] 2. Construction of an Uncoupling Protein 1 Donor Plasmid

[0044] Firstly, the Pcdna3.1 plasmid was double-enzyme digested using Kpn I endonuclease and Xho I endonuclease, and the adiponectin promoter-UCP1 fragment was recovered by electrophoresis. The adiponectin promoter-UCP1 fragment was ligated to the pLB vector using the pLB Zero-Background Simple Fast Cloning Kit (TIANGEN BIOTECH Co., Ltd.), the positive plasmid was identified, and large-scale extraction of the plasmid was performed for later use. Finally, the obtained new plasmid was single-enzyme digested using BspEI enzyme, purified and recovered, and then, the gRNA recognition sequence with BspEI restriction enzyme cutting site, i.e., the target sequence (Bait sequence), was ligated to the linearized plasmid using T4 DNA ligase to obtain the donor plasmid.

[0045] 3. Acquisition of UCP1 Transgenic Fibroblasts 3.1 Construction of Porcine Fetal Fibroblasts

[0046] 1) A Bama sow at day 35 of gestation was killed to give the uterus, and the uterus was transported to the laboratory within 1 hour. The fetus was taken out from the uterus, washed with DPBS containing antibiotics, transferred to a clean bench, and the head, limbs and viscera were removed using ophthalmic scissors. The remainder was washed with DPBS repeatedly until it was clean. The remainder was cut into pieces using ophthalmic scissors in a 100 mm culture dish.

[0047] 2) The shredded tissue was transferred to a new 100 mm culture dish, followed by addition of 10 mL of a digestive solution and digestion in a 5% CO.sub.2 incubator at 37 C. for 4 to 6 h. The components of the digestive solution comprise: DMEM high glucose medium (Gibco) supplemented with 15% fetal bovine serum (Hyclone), 0.032% collagenase IV (Sigma), 25 Kunitz units/mL DNase I (Sigma) and 40 g/mL gentamicin (Sigma). After the digestion was completed, the digested product was collected, and centrifuged at 3000 rpm for 10 min in a centrifuge tube, followed by discarding the supernatant, resuspending the resultant pellet with a culture medium and then centrifuging. Finally, the resuspended tissue was placed in a 25 cm.sup.2 culture dish. The components of the culture medium comprise: DMEM high glucose medium (Gibco) supplemented with 15% fetal bovine serum (Hyclone) and 40 g/mL gentamicin (Sigma).

[0048] 3) Subculture or Cryopreservation was Carried Out when Cells Grow to 80% Confluence.

[0049] 3.2 Transfection of Fetal Fibroblasts with the Targeting Vector

[0050] The fetal fibroblasts were resuscitated two days before transfection in a 25 cm.sup.2 culture dish. Transfection can be carried out when the cells grew to about 70% confluence, and the culture medium was replaced 4 h before transfection. The cells were digested using 0.25% trypsin (Invitrogen), resuspended with an electrotransfer solution, and the Cas9/gRNA plasmid and the donor plasmid were added to the resuspended cells. Transfection was carried out with a nuclear electroporation apparatus (Nucleofector 2b Device, Lonza) using U-023 procedure. The transfected cell suspension was transferred to a 60 mm culture dish and cultured for 48 hours.

[0051] 3.3 Cell Screening and Genotyping

[0052] The cells were digested using 0.25% trypsin (Invitrogen). After the digestion reaction was terminated, the cell density was measured using a hand-held automatic cell counter (Millipore). The cells were inoculated into a 96-well plate using limited dilution method according to the cell density. Then, 100 ul of culture medium was added to each well and only one cell was contained per 100 ul of culture medium. After 3-4 days, the culture medium was replaced. When the cells growed to one hundred percent confluence of the 96-well plate, they were transferred to a 24-well plate. When cells growed to one hundred percent confluence of the 24-well plate, a part of the cells was transferred to a 6-well plate, and a small portion of the cells was further cultured in the 24-well plate for genotyping. Finally, a total of 26 cell colonies were obtained and identified by PCR. It was found that cell colonies with bands at both the 5 junction end and the 3 junction end are transgenic, wherein the colony Nos. 8, 14 and 17 are positive (FIG. 2) for subsequent experiments.

[0053] 4. Preparation of a Nuclear Transfer Embryo and a Cloned Pig

[0054] 4.1 Maturation Culture of Pig Oocytes:

[0055] The ovaries of pig collected from a slaughterhouse were placed in a thermos containing physiological saline comprising penicillin and streptomycin at 37 C., and transported to the laboratory within 1 hour. After washing the ovaries with physiological saline for 3 to 5 times, the follicles with a diameter of 3 to 8 mm on the ovary surface were aspirated with syringes, and the follicular fluid containing oocytes was collected in a 50 mL centrifuge tube and washed with TL-HEPES oocyte-washing liquid for 3 times. Dense cumulus-oocyte complexes (COCs) with uniform cytoplasm containing more than three layers of cumulus cells were selected under a stereomicroscope and transferred into an in-vitro maturation culture solution, and cultured under conditions of 39.0 C. and 5% CO.sub.2 for 42 to 44 h.

[0056] 4.2 Acquisition of a Reconstructed Embryo:

[0057] The oocytes subjected to in-vitro maturation culture for 42 to 44 h were digested with 0.1% hyaluronidase (purchased from Sigma company) to remove the cumulus cells around the oocytes. Under a stereomicroscope, oocytes with uniform cytoplasm, obvious perivitelline space and the first polar body expelled, i.e. MII stage oocytes, were selected and placed in a micro operation drop, the mature oocytes were fixed with a fixing tube such that the polar body was at the direction of 3 o'clock, and the first polar body and about of the surrounding cytoplasm (including nucleus) were sucked out with an enucleation needle having an outer diameter of 20 m. The UCP1 transgenic fibroblast was injected into the perivitelline space of the enucleated oocyte, so that the donor cell was in contact with the oocyte membrane. Then, the oocyte was fused with the donor cell by an electric activation method (BTX Electro-cell Manipulator 200) to obtain a reconstituted embryo. The reconstituted embryo was placed in PZM3 solution, cultured under conditions of 39.0 C. and 5% CO.sub.2 for 14 to 16 h, and then embryo transfer was performed.

[0058] 4.3 Embryo Transfer:

[0059] The reconstituted embryos having been subjected to in-vitro culture for 14 to 16 h were transferred into the fallopian tubes of pseudo-pregnant sows in synchronous estrus, and about 180 embryos were transferred to each sow on average. After 28 days, the sows were examined for pregnancy by ultrasound. If a pig was pregnant, the pregnancy status was monitored every two weeks by ultrasound. The present invention obtained 3 pregnant sows and 12 piglets were successfully delivered.

[0060] 5. Genotyping of UCP1 Gene Knock-in Pigs

[0061] After the pig was born, the ear tissue was taken and DNA was extracted using a genomic DNA extraction kit (TIANGEN BIOTECH Co., Ltd.) for PCR genotyping (FIG. 3).

Example 2: Detection of Cold Resistance of Piglets

[0062] One-month-old transgenic pigs and wild-type pigs were placed in a refrigerator at 4 C. for 4 h. Starting from 0 h, the rectal temperature of pigs was measured by an electronic thermometer (Tianjin Jinming Instrument Co., Ltd.) every 1 hour (FIG. 4). It can be seen from FIG. 4 that the rectal temperature of the transgenic pig was significantly higher than that of the wild-type pig during 1 h to 4 h of cold stimulation. At the same time, the pigs were photographed with an infrared camera (FUR) to record changes in the temperature of the pig's body surface (FIG. 5). It can be seen from FIG. 5 that after cold stimulation, the infrared color of the transgenic pig was significantly stronger than that of the wild-type pig, that is, the temperature of the transgenic pig in the area marked with white line was higher than that of the wild-type pig.

Example 3: Slaughter Index Measurements

[0063] The slaughter experiment was carried out when the pigs were 6 months old. Fasting for 24 hours was performed before slaughtering. The pigs were weighed before slaughtering, subjected to anesthesia and killed by bloodletting. The head, hooves, tail and viscera were removed with retained kidney and leaf fat, and then carcass weight was weighed and recorded. The ratio of the carcass weight to the weight before slaughtering is the dressing rate. The pig carcass was separated from the middle. For the left carcass, lean meat, fat, skin and bone were separated and weighed, respectively, and the proportion of each part in the total was calculated (see FIG. 6). It can be seen from FIG. 6 that there is no difference in the dressing rate between the wild-type pig and the transgenic pig, while the lean meat rate of the transgenic pig is significantly higher than that of the wild-type pig and the fat rate is significantly lower than that of the wild-type pig.

[0064] Although the present invention has been described in detail with the general description and the specific embodiment, it is obvious to a person skilled in the art that some modifications or improvements can be made on the basis of the present invention. Therefore, these modifications or improvements made on the basis of without departing from the spirit of the present invention are intended to be within the protection scope of the present invention.

INDUSTRIAL APPLICABILITY

[0065] The present invention provides a cold-resistant and lean-type transgenic pig and a preparation method therefor. In the present invention, by transferring a mouse uncoupling protein 1 gene into the genome of a pig, a transgenic pig is obtained which can not only resist the cold but also have an increased lean meat rate by reducing fat deposition. The transgenic pig provided in the present invention can not only resist the cold but also have an increased lean meat rate by reducing fat deposition. In the present invention, simultaneous improvement of two important production traits of pigs through site-directed single gene manipulation not only lays a foundation for the application and basic research of genetic editing for big animals, but also provides with breeding researchers a new way of thinking for improving traits of livestock. The transgenic pig and the preparation method thereof have good economic value and application prospects.