首页> 外文期刊>Indian Journal of Animal Research >Genetic polymorphism of melatonin receptor 1A (MTNR1A) gene in Corriedale sheep of Kashmir, India
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Genetic polymorphism of melatonin receptor 1A (MTNR1A) gene in Corriedale sheep of Kashmir, India

机译:印度克什米尔Corriedale绵羊褪黑素受体1A(MTNR1A)基因的遗传多态性

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摘要

The aim of the present work was to explore and characterize the different polymorphic variants of exon II region of MTNR1A gene in 31Corriedale sheep of Kashmir. Genomic DNA was extracted and subjected to PCR for the amplification of the main part of exon II of the ovine MTNR1A gene. PCR products were subjected to restriction enzyme (RE) digestion by Mn/I restriction enzyme and depending upon number of sites in the fragment genotypes were classed as MM, Mm and mm genotypes for Mn/I RE. Representative samples of all identified alleles were sequenced from forward as well as reverse side. Allelic frequencies were 0.62 and 0.38 for allele M and m respectively. The population was observed to be in Hardy-Weinberg equilibrium with regard to allele M and m. Results indicated the existence of polymorphism in the exon II of MTATR1A locus in the breed under study. The various mutational positions recorded in the MTNR1A locus were G169T, G328A, G422A, and C607T. The mutation G422A resulted in amino acid change from Valine to Isoleucine while all other mutations were silent.
机译:本工作的目的是探讨和表征克什米尔31只Corridale绵羊MTNR1A基因外显子II区的不同多态性。提取基因组DNA并进行PCR以扩增绵羊MTNR1A基因的外显子II的主要部分。 PCR产物用Mn / I限制酶进行限制酶(RE)消化,根据片段中基因位点的数目,将Mn / I RE的基因型分为MM,Mm和mm基因型。从正反两面对所有已鉴定等位基因的代表性样品进行测序。等位基因M和m的等位基因频率分别为0.62和0.38。关于等位基因M和m,观察到种群处于Hardy-Weinberg平衡。结果表明MTATR1A基因座外显子II中存在多态性。 MTNR1A基因座中记录的各种突变位置是G169T,G328A,G422A和C607T。 G422A突变导致氨基酸从缬氨酸变为异亮氨酸,而所有其他突变均保持沉默。

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