ADSL gene and method of ADSL gene as genetic marker for inosine monophosphate content of Xupu geese
A technology of goinosinic acid and genetic markers, which is applied in the field of determination of polymorphisms in the ADSL gene, can solve the problems that genetic markers have not been reported yet, and achieve significant application value and economic benefits, as well as the effect of fresh muscle quality
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Embodiment 1
[0036] Example 1 SNP screening of Xupu goose pectoralis inosinic acid-related genes
[0037] Sixty healthy Xupu geese of the same age were selected for the filling-feeding experiment. After 28 days of slaughter, the inosinic acid content in breast muscle was detected by high performance liquid chromatography, and the genomic DNA was extracted from samples with high inosinic acid content and low inosinic acid content.
[0038] According to the goose ADSL gene sequence in GenBank, Primer5.0 was used to design primers covering the entire sequence of exon 9 to exon 10 of the gene. The primer sequence is:
[0039] Forward primer: 5’—CACCCATAAAGGGAACAG—3’
[0040] Reverse primer: 5'—AGCACAGACAGCCAGATT—3'
[0041] Primers were synthesized by Hunan Qingke Biotechnology Co., Ltd. The genomic DNA of Xupu goose was amplified with the above primers respectively.
[0042] PCR: 20 μl reaction system: 12 μl of 2×Master mix, 0.8 μl each of upstream and downstream primers (10 μmol / L), 1 μl...
Embodiment 2
[0047] Example 2 Verification of the SNPs related to the inosinic acid content of Xupu goose pectoralis in production practice
[0048] Twenty healthy Xupu geese aged 80 days and under the same feeding and management conditions were selected for the experiment. After 28 days of feeding, all the tested Xupu geese were slaughtered to detect the content of inosinic acid in breast muscle.
[0049] Genomic DNA extracted from 20 Xupu geese pectoralis tissue samples was amplified using the primers in Example 1, and the SNPs were detected according to the method in Example 1.
[0050] Table 1 PCR reaction system
[0051]
[0052] The PCR cycling parameters are as follows:
[0053] Pre-denaturation at 95°C for 5min; denaturation at 95°C for 30s, annealing at 57.6°C for 30s, extension at 72°C for 45s, a total of 35 cycles; extension at 72°C for 10min, and finally storage at 4°C.
[0054] Genotype frequency analysis of ADSL gene SNP locus
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