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首页> 外文期刊>American journal of animal and veterinary sciences >Study and identification of Insulin-like Growth Factor-I gene polymorphisms in Zel sheep population.
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Study and identification of Insulin-like Growth Factor-I gene polymorphisms in Zel sheep population.

机译:Zel绵羊群体中胰岛素样生长因子-I基因多态性的研究与鉴定。

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Problem statement: The IGFs play an important role in regulating somatic growth according to nutritional conditions. Polymorphisms of IGF gene are reported to be significantly associated with many traits. Approach: In these study 142 samples of DNA from Zel sheep were used for detecting the polymorphisms of promoter region of the Insulin-like Growth Factor-1 (IGF-1) gene. Therefore DNA extracted from blood using Salting-out procedure. Results: Primers were supplied for amplifying the specific segment. Polymerase Chain Reaction (PCR) accomplished after finding the best condition to do the reaction. The specific segment amplified well. SSCP and RFLP markers were used for detecting the polymorphisms of the segment. For SSCP analysis PCR-product was denatured and dilution was loaded onto a 12% polyacrylamide gel. RFLP analysis was performed by incubating of PCR product by HaeII restriction enzyme at 37 degrees C for 4 h. Gels were visualized using a 3.5% agarose gel that contained ethidium bromide. The polymorphisms were the same when both methods were examined. Evaluation of result revealed 2 alleles and 3 genotypes. The alleles were A and B and their frequencies was 0.71 and 0.29 respectively. The genotyped named AA, AB and BB with the frequencies of 0.47, 0.47 and 0.06 respectively. Conclusion/Recommendations: The data were analyzed for Genetic variation statistics using PopGene32 software and no deviation from Hardy-Weinberg equilibrium was observed in this study. finding the relation between genotype which is found by genetic markers with growth traits, live weight and carcass weight will be investigate by the IGFs genes.
机译:问题陈述:IGF在根据营养状况调节体细胞生长中起重要作用。据报道,IGF基因的多态性与许多性状显着相关。方法:在这些研究中,使用了142个来自Zel绵羊的DNA样本来检测胰岛素样生长因子1(IGF-1)基因启动子区域的多态性。因此,使用盐析法从血液中提取DNA。结果:提供了用于扩增特定片段的引物。找到最佳条件进行反应后即可完成聚合酶链反应(PCR)。特定片段扩增良好。 SSCP和RFLP标记用于检测片段的多态性。为了进行SSCP分析,将PCR产物变性,并将稀释液加载到12%聚丙烯酰胺凝胶上。通过用HaeII限制酶将PCR产物在37°C下孵育4小时来进行RFLP分析。使用包含溴化乙锭的3.5%琼脂糖凝胶将凝胶可视化。当两种方法都检查时,多态性是相同的。结果评估显示2个等位基因和3个基因型。等位基因为A和B,频率分别为0.71和0.29。该基因型分别为AA,AB和BB,频率分别为0.47、0.47和0.06。结论/建议:使用PopGene32软件对数据进行遗传变异统计分析,本研究未观察到与Hardy-Weinberg平衡的偏差。通过IGFs基因研究寻找具有生长性状的遗传标记物发现的基因型,活体重量和car体重量之间的关系。

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