Method for evaluating, detecting and/or predicting beef quality traits of consumption cattle
A technology for quality traits and beef, applied in biochemical equipment and methods, microbiological determination/inspection, DNA/RNA fragments, etc., can solve problems such as unreported research
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Embodiment 1 4
[0057] Example 1 Amplification of Sichuan Yak ACOT12 Gene SNP Site
[0058] 1. Experimental samples
Embodiment 1
[0059] The 102 Sichuan yaks in Example 1 came from a cattle farm in Aba Prefecture, Sichuan Province. The blood samples of healthy yaks in the same environment, the same feeding conditions, and the same period were collected and stored at -20°C for the extraction of blood genome DNA and the collection of related meat Quality trait data and analysis.
[0060] 2. Experimental method
[0061] 1. DNA extraction
[0062] According to the instructions, the blood genome DNA extraction kit was used to extract DNA from Sichuan yak blood samples, the concentration and purity of DNA were detected by micro-spectrophotometer, and the quality of DNA was detected by agarose gel electrophoresis.
[0063] 2. Primer design
[0064] According to the bovine ACOT12 gene sequence published in Ensembl (ENSBTAT00000014753.6), a pair of specific amplification primers was designed and synthesized by Sangon Bioengineering (Shanghai) Co., Ltd.
[0065] The sequences of the specific amplification prime...
Embodiment 2
[0080] Example 2 Population genetic characteristics of 3 SNPs loci of ACOT12 gene
[0081] 1. Experimental method
[0082] All 102 Sichuan yak sequencing results obtained in Example 1 were analyzed, using Popgene 32 software to calculate the gene frequency, genotype frequency, genetic heterozygosity (H), effective allele number (Ne) of alleles; PIC0.6 software calculates polymorphic information content (PIC).
[0083] 2. Experimental results
[0084] The population genetic characteristics of the three SNPs of the ACOT12 gene are shown in Table 1. It can be seen from Table 1 that the dominant genotype in SNP site 1 (E1-285T>C), SNP site 2 (E1-603 T>A), and SNP site 3 (E1-675 C>G) is TC , TA, CC, the dominant alleles are T, A, C, respectively, and the frequency is greater than 0.5.
[0085] The genetic heterozygosity (H) and polymorphic information content (PIC) of SNP locus 1 (E1-285 T>C) and SNP locus 2 (E1-603 T>A) were between 0.25 and 0.50, It shows that the above loci...
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