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Genotyping of β-Lactoglobulin gene by PCR-RFLP in Sahiwal and Tharparkar cattle breeds

机译:通过PCR-RFLP对Sahiwal和Tharparkar牛品种的β-乳球蛋白基因进行基因分型

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摘要

BackgroundImprovement of efficiency and economic returns is an important goal in dairy farming, as in any agricultural enterprise. The primary goal of dairy industry has been to identify an efficient and economical way of increasing milk production and its constituents without increasing the size of the dairy herd. Selection of animals with desirable genotypes and mating them to produce the next generation has been the basis of livestock improvement and this would continue to remain the same in the coming years. The use of polymorphic genes as detectable molecular markers is a promising alternative to the current methods of trait selection once these genes are proven to be associated with traits of interest in animals. The point mutations in exon IV of bovine β-Lactoglobulin gene determine two allelic variants A and B. These variants were distinguished by Polymerase Chain Reaction and Restriction Fragment Length Polymorphism (PCR-RFLP) analysis in two indigenous Bos indicus breeds viz. Sahiwal and Tharparkar cattle. DNA samples (228 in Sahiwal and 86 in Tharparkar) were analyzed for allelic variants of β-Lactoglobulin gene. Polymorphism was detected by digestion of PCR amplified products with Hae III enzyme, and separation on 12% non-denaturing gels and resolved by silver staining.
机译:背景技术与任何农业企业一样,提高效率和经济回报是奶牛养殖的重要目标。奶业的主要目标是确定一种有效且经济的方式来增加奶产量及其组成,而不增加奶牛群的规模。选择具有理想基因型的动物并将它们交配以生产下一代已成为牲畜改良的基础,并且在未来几年中这种情况将保持不变。一旦证明这些基因与动物感兴趣的性状有关,使用多态性基因作为可检测的分子标记物是当前性状选择方法的有前途的替代方法。牛β-乳球蛋白基因外显子IV上的点突变确定了两个等位基因变体A和B。这些变体通过聚合酶链反应和限制性片段长度多态性(PCR-RFLP)分析在两个本地博斯印度品种中进行区分。 Sahiwal和Tharparkar的牛。分析了DNA样本(Sahiwal中为228个,Tharparkar中为86个)的β-乳球蛋白基因等位基因变体。通过用Hae III酶消化PCR扩增产物,并在12%非变性凝胶上分离并通过银染来解决多态性。

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