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首页> 外文期刊>Iranian Journal of Applied Animal Science >Association between Yearling Weight and Calpastatin and Calpain Loci Polymorphism in Iranian Zel Sheep
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Association between Yearling Weight and Calpastatin and Calpain Loci Polymorphism in Iranian Zel Sheep

机译:一岁体重与钙蛋白酶抑素和伊朗Zel绵羊钙蛋白酶基因座多态性的关联

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Genotypes of Iranian Zel sheep for Calpastatin(CAST) locus were determined by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) and polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) methods and for Calpain(CAPN) locus by PCR-SSCP. Blood samples were collected from 200 purebred Zel sheep of Zel Breeding Station located in Golestan province in northeast of Iran. Extraction of genomic DNA was based on modified salting out method. The digestion of PCR products of CAST gene by MspI and NcoI restriction enzymes revealed two alleles M and N, with frequencies 85.5 and 14.5%, respectively. Frequencies were 75, 21 and 4% for MM, MN and NN genotypes, respectively. Alternatively, using PCR-SSCP method, four genotypes including AA, AB, BB and AC with frequencies of 71, 21, 4 and 4%, respectively, were observed in this population. Analyzing CAPN gene by the PCR-SSCP method, revealed two different conformational patterns (AA and AB) with frequencies of 69 and 31% for AA and AB, respectively. Average heterozygosity for both loci was low (0.28 and 0.25% for CAST using PCR-SSCP and PCR-RFLP, and 0.26% for CAPN).Yearling weights (YW) were analyzed by a statistical model comprising PCR-SSCP and as a result CAPN genotypes had significant effect (P<0.01) on YW. A Chi-square test confirmed Hardy-Weinberg (H-W) equilibrium for the CAST locus using PCR-SSCP method but not for PRC-RFLP method and CAPN locus. Totally, the investigated herd had little genetic diversity and different factors disturb H-W equilibrium and PCR-RFLPand PCR-SSCP might be used successfully in these studies.
机译:通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)和聚合酶链反应-单链构象多态性(PCR-SSCP)方法确定伊朗Zel绵羊的基因型,钙蛋白酶(CAPN)座位的基因型通过PCR-SSCP。采血是从位于伊朗东北部Golestan省的Zel育种站的200只纯种Zel绵羊采集的。基因组DNA的提取是基于改良的盐析法。 MspI和NcoI限制性内切酶消化CAST基因的PCR产物显示两个等位基因M和N,频率分别为85.5和14.5%。 MM,MN和NN基因型的频率分别为75%,21%和4%。或者,使用PCR-SSCP方法,在该人群中观察到了四种基因型,分别为AA,AB,BB和AC,频率分别为71%,21%,4%和4%。通过PCR-SSCP方法分析CAPN基因,发现两种不同的构象模式(AA和AB),AA和AB的频率分别为69%和31%。两个基因座的平均杂合度均较低(使用PCR-SSCP和PCR-RFLP的CAST的平均杂合度为0.28和0.25%,CAPN的为0.26%)。通过包含PCR-SSCP的统计模型分析了年体重基因型对黄W病有显着影响(P <0.01)。卡方检验使用PCR-SSCP方法确认了CAST基因座的Hardy-Weinberg(H-W)平衡,而PRC-RFLP方法和CAPN基因座则没有。总体而言,所研究的牛群遗传多样性很少,并且各种因素干扰了H-W平衡,PCR-RFLP和PCR-SSCP可能成功用于这些研究。

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