首页> 外文期刊>African Journal of Biotechnology >Detection of polymorphism of the insulin-like growth factor-I (IGF-I) gene in Mazandaran native chicken using PCR-RFLP method
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Detection of polymorphism of the insulin-like growth factor-I (IGF-I) gene in Mazandaran native chicken using PCR-RFLP method

机译:PCR-RFLP法检测马赞达兰天然鸡胰岛素样生长因子-I(IGF-I)基因的多态性

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摘要

Molecular genetic selection on individual genes is a promising method to genetically improve economically important traits in chickens. The insulin-like growth factor-I (IGF-I)?gene may play important roles in growth of multiple tissues, including muscle cells, cartilage and bone. In the present study, polymorphism of the promoter and 5' untranslated region of IGF-I gene of Mazandaran native fowls was investigated. In order to evaluate the IGF-I gene polymorphism, we used the restriction fragment length polymorphism (RFLP) method. Blood samples were collected from randomly chosen 100 Mazandaran native fowls. Genomic DNA was extracted using modified salting-out method and amplified polymerase chain reaction technique. The promoter and 5' untranslated region of the fowl IGF-I gene was amplified to produce a 621 bp fragment. The PCR products were electrophoresed on 2.5% agarose gel and stained by ethidium bromide. Then they were digested of amplicons with PstI, which revealed two alleles A and B. Data were analyzed using Pop Gene 32 software package. In this population, AA, AB, BB genotypes were identified with 25.88, 50.23 and 23.89% frequencies, respectively. Allele frequencies (A and B) were 0.51 and 0.49, respectively. The Chi-square (χ2) test did not show deviation from Hardy–Weinberg equilibrium (P<0.05).
机译:对单个基因进行分子遗传选择是从遗传上改善鸡的重要经济性状的有前途的方法。胰岛素样生长因子-I(IGF-I)?基因可能在包括肌肉细胞,软骨和骨骼在内的多种组织的生长中起重要作用。在本研究中,研究了马赞达兰家禽IGF-I基因启动子和5'非翻译区的多态性。为了评估IGF-I基因多态性,我们使用了限制性片段长度多态性(RFLP)方法。从随机选择的100只Mazandaran本地家禽中采集血样。使用改良的盐析法和扩增的聚合酶链反应技术提取基因组DNA。禽IGF-1基因的启动子和5′非翻译区被扩增以产生621bp的片段。将PCR产物在2.5%琼脂糖凝胶上电泳,并用溴化乙锭染色。然后用PstI消化扩增子,揭示出两个等位基因A和B。使用Pop Gene 32软件包分析数据。在该人群中,分别以25.88%,50.23%和23.89%的频率鉴定出AA,AB,BB基因型。等位基因频率(A和B)分别为0.51和0.49。卡方检验(χ2)并未显示出与Hardy-Weinberg平衡的偏离(P <0.05)。

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