Method for detecting pig hair-free character based on EDAR gene expression quantity and application thereof
A gene expression and expression technology, applied in the direction of DNA / RNA fragments, recombinant DNA technology, biochemical equipment and methods, etc., can solve the problems of unassisted hairless pig selection and breeding, etc., to reduce the existence of false positives and achieve accurate results Effect
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Embodiment 1
[0039] Example 1: Screening for the gene EDAR associated with hairless traits
[0040] The experimental population of the present invention is a small amount of large white hairless pigs discovered earlier (discovery address: Anping County, Hengshui City, Hebei Province, discoverer: Ding Xiangdong, associate researcher of the Animal Science and Technology College of China Agricultural University)
[0041] The specific implementation of EDAR screening:
[0042] S1. Hairless pig mating plan: select normal boars and hairless sows for mating, and perform cesarean section when pregnant sows reach 41 days of gestation, take out pig embryos and collect two tissue pieces of 2cm x 2cm on the back of the embryos, and then separate the skin tissue And disinfect. One of them was placed in liquid nitrogen for RNA preservation, and the other was placed in paraformaldehyde for later phenotypic identification.
[0043] S2. Phenotype identification: for phenotype identification, hematoxylin ...
Embodiment 2
[0058] Example 2 Verification of the relationship between EDAR gene expression and hairless phenotype in pig skin (experimental verification of the relationship between EDAR quantitative values and hairless traits)
[0059] S1. Hairless pig breeding plan: select normal boars and hairless sows to breed, and perform cesarean section when pregnant sows reach 41 days of gestation, take out pig embryos and collect two tissue pieces of size 2cm x 2cm on the back of the embryos, then separate the skin tissue and dry Disinfect. Place samples in liquid nitrogen for RNA preservation.
[0060] S2. mRNA extraction of skin samples: Grind the tissue block into powder in liquid nitrogen, weigh 50-100 mg of the tissue sample, add 1 ml Trizol, and then perform homogenization. Using chloroform (trichloromethane), isopropanol, 75% ethanol, and RNase-free water (required to be prepared with DEPC-treated water), the protein, DNA, and inorganic salts in the tissue were eluted and removed, and th...
Embodiment 3
[0085] Example 3 Breeding Homozygous Hairless Pigs by Gene Editing EDAR Knockout Pigs
[0086] Hairless pigs were gene-edited using CRISPR / Cas9 gene knockout technology, and the molecular mechanism of EDAR on the formation of hair follicle placodes and the effect of hair follicle phenotype were verified by knockout of EDAR. The phenotype data of EDAR knock-in pig hair follicles were collected and analyzed to verify that EDAR is a functional gene that affects the formation of hair follicle placodes and leads to hairless traits.
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