Molecular Markers and Detection Methods of Holstein Cattle Heat Stress Tolerance
A technology of Holstein cattle and heat stress, applied in the direction of biochemical equipment and methods, microbial measurement/inspection, etc., can solve problems such as lack of
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Embodiment 1
[0106] Example 1. Genome-wide association analysis of rectal temperature of Holstein cattle under heat stress conditions
[0107] 1. Determination of rectal temperature
[0108] From 2013 to 2015, the rectal temperature of Holstein lactating cows under heat stress in 9 pastures in Beijing was measured every summer (June to August), a total of 6,446 cows. Measuring time: 7:00 to 10:00 in the morning and 14:00 to 17:00 in the afternoon (according to NY / T 2363-2013, when the average temperature and humidity index of the barn is 72≤THI≤79, Holstein cattle In a state of mild heat stress; when the average temperature and humidity index of the barn is 7888, the Holstein cattle are in a severe heat stress state. Stress state), each cow measured rectal temperature twice a day, recorded as rectal temperature in the morning and rectal temperature in the afternoon, and measured for two consecutive days. Measuring method: When measuring, the cow is under the neck yoke, and the electronic...
Embodiment 2
[0120] Example 2 Screening and polymorphism mining of candidate genes related to heat stress tolerance
[0121] In order to find candidate genes that may be related to heat stress tolerance, the 200kb regions near the significant SNPs were selected as candidate regions, and the gene screening was carried out. A total of 5 candidate genes that may be related to EBV in the rectal temperature in the morning were found (Table 1). After reviewing the literature, it was found that the protein encoded by the PHRF1 gene is rich in the Ser / Arg domain, which binds to the C-terminus of the large subunit of RNA polymerase II, and can promote genomic DNA by regulating non-homologous end joining after DNA damage. For completeness, we therefore speculate that PHRF1 is the most likely functional candidate gene. In order to further verify the possibility of the PHRF1 gene as a candidate gene, its polymorphism was screened and its association with traits was analyzed.
[0122] 1. Genomic DNA ...
Embodiment 3
[0152] Example 3. SNPs group typing and its correlation analysis with various physiological indicators and milk production performance EBVs of Holstein cattle under heat stress
[0153] Randomly select 1,665 Holstein lactating cows with clear pedigree, complete phenotype and DHI records from Beijing area as the experimental group, collect 10 mL of anticoagulated blood intravenously, and then take 800 μL of blood, and use the blood genome extraction kit (article number: DP318-03, Tiangen Biochemical Technology (Beijing) Co., Ltd.), DNA extraction was performed according to the instructions. Use NanoDrop2000 ultraviolet spectrophotometer and 1% agarose gel electrophoresis (130V, 20min) to detect the quality of DNA extraction, and store the qualified DNA in a -20°C refrigerator for future use.
[0154] 1. Establishment of a large group typing method for SNPs of the PHRF1 gene
[0155] Each individual SNP genotype was obtained using competitive allele-specific PCR (KASP). Compet...
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