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首页> 外文期刊>African Journal of Biotechnology >Diversity of growth hormone gene and its relation with average daily gain in Simmental cattle in West Sumatera Province, Indonesia
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Diversity of growth hormone gene and its relation with average daily gain in Simmental cattle in West Sumatera Province, Indonesia

机译:印度尼西亚西苏门答腊省西门塔尔牛生长激素基因的多样性及其与日平均增重的关系

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摘要

This study was aimed to analyse the genetic polymorphism of Growth Hormone (GH) polymorphism of Simmental cattle using polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method and its relation to average daily gain. The research was conducted in the Padang Mangatas Breeding Centre, Limapuluh Kota district, West Sumatera Province and Biotechnology Laboratory of Faculty of Animal Husbandry, Andalas University. The research used 100 Simmental calves. DNA were isolation from blood sample using DNA purification Kit from Pomega. The PCR procedure was used to amplify 591-bp of bGH exon 1 (GH1) and 694-bp exon 2 (GH2). The PCR product were digested by restriction enzymes MspI and AluI. Digestion of 591-bp GH gen PCR product with enzyme restriction MspI reveal allele A(+) and B(-) with frequency 0.875 and 0.125 respectively and digestion with restriction enzyme AluI revealed allele C(+) and D(-) with frequency 0.95 and 0.05 respectively and. Digestion of 694-bp PCR product by MspI represent allele P(+) and Q(-) with frequency 0.88 and 0.12 respectively and digestion with AluI enzyme represent allele R(+) and S(-) with frequency 0.94 and 0.06 respectivly. The observed heterozygosity, effective allele numbers and polymorphism information content of GH1/MspI, GH2/MspI, GH1/AluI, and GH2-AluI were 0.11/0.1948, 0.04/0.1889, 0.00/0.0927, and 0.00/0,1096 respectively. Using GLM, there was no relation between these polymorphic and avarage daily gain of calve.
机译:本研究旨在利用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法分析西门塔尔牛生长激素(GH)多态性的遗传多态性及其与平均日增重的关系。这项研究是在西苏门答腊省利马普鲁亚哥打区的Padang Mangatas繁育中心和安达拉斯大学畜牧学院生物技术实验室进行的。该研究使用了100只西门塔尔牛犊。使用Pomega的DNA纯化试剂盒从血液样本中分离DNA。 PCR程序用于扩增591 bp的bGH外显子1(GH1)和694 bp的外显子2(GH2)。用限制酶MspI和AluI消化PCR产物。酶切MspI的591 bp GH基因PCR产物的消化分别显示频率为0.875和0.125的等位基因A(+)和B(-),酶切AluI的消化显示频率为0.95的等位基因C(+)和D(-)和0.05分别和。 MspI消化694-bp PCR产物分别代表频率为0.88和0.12的等位基因P(+)和Q(-),而用AluI酶消化分别代表频率为0.94和0.06的等位基因R(+)和S(-)。 GH1 / MspI,GH2 / MspI,GH1 / AluI和GH2-AluI的杂合度,有效等位基因数和多态性信息含量分别为0.11 / 0.1948、0.04 / 0.1889、0.00 / 0.0927和0.00 / 0,1096。使用GLM,这些多态性与平均小牛日增重之间没有关系。

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