A set of SNP molecular markers for screening and/or detecting the abnormality rate of spermatozoa in breeding bulls
A technology for sperm deformity and bulls, applied in the field of molecular genetic biology, can solve problems such as functional verification that has not been reported, and achieve the effects of increasing farm economic benefits, high accuracy and reducing costs
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Embodiment 1
[0031] Identification of the SNP site and genotype combination of embodiment 1 bovine PRKCB gene
[0032] The invention adopts the PCR product direct sequencing method to carry out SNP identification and typing on the PRKCB gene of Chinese Holstein bulls.
[0033] 1.1 Experimental materials
[0034] The bull used in the present invention is selected from Shandong Oakes bull station, 117 Chinese Holstein bulls. Frozen bull semen was stored in liquid nitrogen for later use.
[0035] 1.2 Extraction of genomic DNA from frozen semen
[0036] The high-salt method was used to extract the genomic DNA from the frozen semen, and the purity and concentration of the DNA samples were detected by a nucleic acid and protein analyzer, and finally diluted to 50 ng / μl, and stored at 4°C for later use.
[0037] 1.3 Design of primers
[0038] According to the bovine PRKCB gene sequence (accession number: AC_000182) provided by NCBI, utilize Primer Premier5.0 software to design primers, the se...
Embodiment 2
[0050] Example 2 Correlation Analysis of Bovine PRKCB Gene Haplotype Combination and Bull Sperm Motility
[0051] SAS 9.0 was used to compare the correlation between different genotype combinations of PRKCB gene and sperm abnormality rate in Chinese Holstein bulls. Its model is:
[0052] Y ijk =μ+G i +H k +e ijk
[0053] Y ijk is the observed value of the trait of sperm deformity in bulls; μ is the average value of the population; G i : fixed effect of haplotype combination; H k : fixed effect of the number of sessions; e ijk : random residual effect.
[0054] The results of haplotype combination correlation showed that among the six genotype combinations, the sperm abnormality rate of bulls with H1H2 haplotype combination was significantly lower than that of bulls with H1H1 and H2H2 haplotype combination (P<0.05) (Table 1).
[0055] Table 1 Correlation analysis between different haplotype combinations of bovine PRKCB gene and semen quality
[0056]
[0057] Note...
Embodiment 3
[0060] Embodiment 3 detection kit
[0061] As described in Example 1, bovine PRKCB genes g.-1526C>T, g.-1409C>T, g.-1259C>T, g.-1249A>G, g.-1230C>T, g.-1220C> T, g.-1091C>T, g.-1089C>T, g.-1088C>T, g.-1081A>T, g.-869A>C and g.-806A>C are all related to bull sperm deformity rate are closely related. Therefore, it is possible to invent a PRKCB gene SNPs molecular marker detection kit suitable for screening the abnormality rate of male bulls.
[0062] 1.1 PCR-RFLP genotyping
[0063] Since the 12 SNPs in the PRKCB promoter region are completely linked, the genotype of the overall SNPs can be obtained by detecting the genotype of any one of the SNPs. Here, we take the g.-1259C>T site as the detection point, as long as the g.-1259C>T site genotype is detected, the genotypes of the remaining 11 SNPs sites can be known. In order to find a simpler method, we use the PCR-RFLP method to identify the genotype of one of the SNPs, and then we can know the genotype of the entire SNPs co...
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