Molecular marker on pig chromosome No.7 related to duroc pig daily weight gain property and application
A molecular marker and chromosomal technology, applied in recombinant DNA technology, microbial determination/inspection, DNA/RNA fragments, etc., which can solve the problem that QTL cannot be accurately located at one time, multiple traits cannot be analyzed at one time, and QTL mapping resolution is poor. and other problems to achieve the effect of increasing core competitiveness, reducing feeding costs, and 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] Embodiment 1 concrete explanation obtains the assay process that affects daily weight gain in the present invention
[0035] The average daily gain of live pigs from 30 kg to 100 kg body weight was measured by the Osborne FIRE Pig Performance Testing System (Kansas, NE, USA). The experimental pig group used in the present invention is 2121 purebred plus-line Duroc of Guangdong Wen's Food Group Co., Ltd. Breeding Pig Branch Company, which is the core group of the Breeding Pig Branch Company, and the group pedigree records are detailed. In this experiment, the Canadian Duroc breed pigs in this resource group were selected. 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.
Embodiment 2
[0036] Embodiment 2 specifically explains the inventive process of obtaining the gene marker in the present invention
[0037] (1) The method of extracting DNA from the ear-like tissues of the Canadian Duroc pig was extracted from the whole genome DNA according to the marked phenol-chloroform method. Using Nanodrop-ND1000 spectrophotometer to detect the quality and concentration of the DNA of the purebred plus line Duroc population. The ratio of A260 / 280 is 1.8-2.0, and the ratio of A260 / 230 is 1.7-1.9. Finally, the qualified DNA samples were uniformly diluted to 50 ng / μl.
[0038] (2) 50K SNP genotype detection of the whole pig genome: GeneSeek Genomic Profiler Porcine50KSNP typing platform, using Illumina Infinium instructions and standard procedures for chip hybridization and result scanning. Finally, the genotype data were read by GenomeStudio software. The quality control of the obtained genotype data was performed with PLINK v1.07, and the detection rate was -6 Indivi...
Embodiment 3
[0044] Embodiment 3 specifically explains the inventive process of inventing and detecting SNP markers
[0045] (1) The target segment containing the SNP site significantly related to the average daily weight gain of the Canadian Duroc 30-100 kg is a 214bp nucleotide sequence in chromosome 7, and the upstream and downstream primers for sequence amplification are primer-F and primer-R, its nucleic acid sequence is as follows:
[0046] Upstream primer primer-F: 5'-CCAGGAGAACTGGGTCACAT-3';
[0047] Downstream primer primer-R: 5'-TGGCTCATTCAGTGCAGAAC-3';
[0048] (2) PCR amplification system and condition setting
[0049] Configure a 10 μL system, including 1.0 μL DNA sample, 0.3 μL upstream primer, 0.3 μL downstream primer, 5.0 μL PCR mix, ddH 2 O3.4 μL, PCR conditions were pre-denaturation at 95°C for 5 min, denaturation at 95°C for 30 s, annealing at 64°C for 30 s, extension at 72°C for 30 s, a total of 35 cycles, and a final extension at 72°C for 5 min.
[0050] (3) DNA se...
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