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首页> 外文期刊>Russian journal of genetics >Polymorphism within the intron region of the bovine leptin gene in Iranian Sarabi cattle (Iranian Bos taurus)
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Polymorphism within the intron region of the bovine leptin gene in Iranian Sarabi cattle (Iranian Bos taurus)

机译:伊朗Sarabi牛(伊朗Bos taurus)牛瘦素基因内含子区域内的多态性

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摘要

The main goal of breeders is breeding superior animals. Most traits of the economic importance in farm animals are determined by polygenic loci and environmental factors. Progress in animal breeding may be improved by combining traditional performance data with molecular genetic information on quantitative loci in selection index. Candidate genes are chosen for study on the basis of known relationships between biochemical and physiological processes. Leptin is 16 kDa protein that is synthesized by adipose tissue and it is involved in the regulation of feed intake, energy balance, fertility, and immune functions. In cattle, the leptin gene is located on chromosome 4. It consists of three exons and two introns, of which only two exons are translated into protein. Sixty-six animals were genotyped for this project. PCR was carried out between exon 2 (intron 2). A strategy employing polymerase chain reaction was used to amplify a 422 bp from blood, semen, hair root, and milk DNA. Digestion of polymerase chain reaction products with Sau3AI revealed two alleles: allele A was 390, 32 fragments and allele B was 303, 88, 32 (only 303 fragment visible on the gel). Three patterns were observed and frequencies were 0.31, 0.43, and 0.14 for AA, AB and BB, respectively. This polymorphism could be further evaluated for marker-assisted selection and developed PCR methodology would expedite screening for large numbers of animals required for such studies.
机译:育种者的主要目标是繁殖优质动物。在农场动物中具有经济重要性的大多数特征是由多基因位点和环境因素决定的。通过将传统的性能数据与选择位点上定量位点的分子遗传信息相结合,可以改善动物育种的进展。根据生化和生理过程之间的已知关系选择候选基因进行研究。瘦素是由脂肪组织合成的16 kDa蛋白,它参与饲料摄入,能量平衡,生育力和免疫功能的调节。在牛中,瘦素基因位于4号染色体上。它由三个外显子和两个内含子组成,其中只有两个外显子被翻译成蛋白质。该项目对66只动物进行了基因分型。在外显子2(内含子2)之间进行PCR。使用聚合酶链反应的策略用于从血液,精液,发根和牛奶DNA扩增422 bp。用Sau3AI消化聚合酶链反应产物可发现两个等位基因:等位基因A为390个32个片段,等位基因B为303个,88个,32个(在凝胶上仅可见303个片段)。观察到三种模式,AA,AB和BB的频率分别为0.31、0.43和0.14。可以进一步评估这种多态性以进行标记辅助选择,而发达的PCR方法将加快筛选此类研究所需的大量动物的速度。

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