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Analysis of polymorphism at the beta-lactoglobulin locus in vechur and dwarf cattle of Kerala using PCR-RFLP

机译:使用PCR-RFLP分析喀拉拉邦的侏儒牛和矮牛中β-乳球蛋白基因座的多态性

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Investigations were carried out on the genetic polymorphism at the beta-lactoglobulin (beta-LG) locus in Vechur and nondescript dwarf cattle of Kerala, using the PCR-RFLP method. A total of 92 Vechur cattle and 34 dwarf cattle were studied. A 262 bpregion of the beta-LG gene spanning from exon IV to intron IV that contains the nucleotide substitution diagnostic of A or B allele was amplified by polymerase chain reaction and polymorphism was detected by digestion of the PCR product with HaeIII enzyme. The analysis revealed two alleles; namely, allele A (153 and 109 bp) and allele B (109, 79 and 74 bp). The frequencies of beta-LG-A and beta LG-beta alleles were 0.35/0.65 and 0.19/0.81 for Vechur and dwarf cattle, respectively. The frequencies of different genotypes in two types of cattle were AA: 0.11, 0.03; AB: 0.48, 0.32 and BB: 0.41, 0.65, respectively. The observed numbers of the three beta-LG genotypes were not significantly (p > 0.05) different from the expected numbers on the basis of Hardy-Weinberg equilibrium. It was important to note that the frequency of the desirable B allele was very high in both the cattle types investigated.
机译:使用PCR-RFLP方法,对喀拉拉邦的Vechur和非描述性矮矮牛的β-乳球蛋白(β-LG)基因座进行了遗传多态性研究。共研究了92头Vechur牛和34头矮人牛。通过聚合酶链反应扩增了包含外显子IV到内含子IV的β-LG基因的262 bp区域,该区域包含诊断A或B等位基因的核苷酸,通过聚合酶链反应扩增了多态性,并用HaeIII酶消化了PCR产物。分析发现了两个等位基因。即等位基因A(153和109 bp)和等位基因B(109、79和74 bp)。 Vechur和矮牛的β-LG-A和β-LG-β等位基因频率分别为0.35 / 0.65和0.19 / 0.81。两种类型的牛的不同基因型的频率分别为AA:0.11、0.03; AA:0.11、0.03。 AB:0.48、0.32和BB:0.41、0.65。在Hardy-Weinberg平衡的基础上,观察到的三种β-LG基因型数目与预期数目没有显着差异(p> 0.05)。重要的是要注意,在所调查的两种牛中,理想的B等位基因的频率都很高。

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