Single nucleotide polymorphisms (SNP) molecular marker located on porcine chromosome 1 and related to daily gain of pig and application of SNP molecular marker
A molecular marker and chromosome technology, applied in the field of molecular biotechnology and molecular markers, can solve the problems of restricting the application of molecular markers for complex traits, unable to confirm genes, and large span of candidate gene regions, so as to increase core competitiveness, increase gene frequency, The effect of speeding up the breeding process
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0034] 1. Experimental animals
[0035] The group of experimental pigs used in the present invention is 3916 purebred American Durocs from the breeding pig branch of Wen's Food Group Co., Ltd., which is the core group of the breeding pig branch, and the group pedigree records are detailed. In the breeding process of 3916 American Duroc pigs in the resource group selected in this experiment, the pigs have free access to food and water, and the entire feeding method and feeding conditions are always consistent, which is a conventional method.
[0036] 2. Sample collection
[0037] The above-mentioned piglet docked tail and ear tissues were collected, soaked in ethanol with a volume fraction of 75%, and stored in a -20°C refrigerator for later use.
[0038] 3. 50K SNP typing in the whole pig genome
[0039] The ear tissue or docked tail tissue collected from each individual of the 3916 Duroc breeding pigs selected from the above-mentioned resource groups, the whole genome DNA w...
Embodiment 2
[0049] Example 2 Target DNA sequence amplification and sequencing
[0050] (1) Primer design
[0051] The DNA sequence of SEQ ID NO: 1 on pig chromosome 1 was downloaded from the Ensembl website (http: / / asia.ensembl.org / index.html). And use primer design software primer premier 6.0 to design primers.
[0052] The DNA sequences of the designed primers are as follows:
[0053] P001-F: 5'-CTGTGTCCCAAAGATCCCTGT-3',
[0054] P002-R: 5'-TGATGAGTGACCAGGCAGAG-3';
[0055] (2) PCR amplification
[0056] Add 1 μL of DNA template, 3.4 μL of double distilled water, 5 μL of 2×Tag PCR StanMix with Loading Dye, and 0.3 μL of primers P001-F and P002-R into a 10 μL reaction system. The PCR reaction conditions were as follows: 5 minutes of pre-denaturation at 94°C, 35 cycles of denaturation at 94°C for 30 s, annealing at 55°C for 30 s, extension at 72°C for 45 s, and finally 5 min at 72°C.
[0057] (3) DNA sequence determination
[0058] The identification of DNA sequence sequencing was ...
Embodiment 3
[0062] Example 3 SNP site g.87T>C effect analysis of molecular markers
[0063] The invention provides a SNP marker that can significantly increase the daily weight gain of Duroc pigs, and the SNP can be used for marker-assisted selection, which can greatly increase the breeding process of the lean meat rate of Duroc pigs. Through the assisted selection of molecular markers, if the present invention selects all the CC-type individuals with molecular markers that affect the daily weight gain traits of pigs into TT-type individuals, assuming that the pigs are bred to 160 days for slaughter, then each pig can gain 1.76kg more weight. According to the estimation of the slaughter rate of 50%, a large-scale pig farm with 10,000 heads can provide 8.8 tons more pork, which will bring huge economic benefits to the enterprise.
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com