首页> 外文期刊>Indian Journal of Biotechnology >PCR-SCCP and sequence analysis of leptin gene reveals novel polymorphism in intron 1 and allele fixation in exon 2 of Indian buffaloes (Bubalus bubalis)
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PCR-SCCP and sequence analysis of leptin gene reveals novel polymorphism in intron 1 and allele fixation in exon 2 of Indian buffaloes (Bubalus bubalis)

机译:PCR-SCCP和瘦素基因序列分析揭示印度水牛(Bubalus bubalis)的内含子1和多态性固定在外显子2中的新型多态性

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The present study was undertaken to delineate single nucleotide polymorphisms within exon 2 and its flanking regions of bubaline leptin gene using polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP) analysis. A total of 118 buffaloes from seven different breeds were studied, revealing three distinct SSCP variants, viz., A, B and C, with a frequency of 0.703, 0.195 and 0.102, respectively. Sequence analysis of the region revealed 9 nucleotide variations including 8 transitions and one transversion as compared to cattle. Two A-G mutations within the coding DNA region were non-synonymous, resulting in change of amino acids. Basic local alignment search tool (BLAST) analysis of bubaline leptin gene revealed a sequence homology of 95-96% with bovines, caprines and ovines, while it varied from 86% to 93% with other farm animal species. Sequence analysis of SSCP variants showed a single nucleotide polymorphism (SNP) within intron 1 with the variant 'A' having homozygous 'T' allele and variant 'B' having homozygous `G' allele, while variant 'C' having heterozygous 'T/G' alleles. The identified SNP locus was found to deviate from Hardy-Weinberg equilibrium with less than expected frequency of heterozygotes. The study also found no variation within exon 2 and complete fixation of unfavorable allele 'C', which has been earlier reported to be associated with lower milk and protein yield in cattle
机译:本研究的目的是利用聚合酶链反应-单链构象多态性(PCR-SSCP)分析来描述大肠瘦素基因外显子2及其侧翼区域内的单核苷酸多态性。共研究了来自七个不同品种的118个水牛,揭示了三个不同的SSCP变体,即A,B和C,其频率分别为0.703、0.195和0.102。与牛相比,该区域的序列分析显示9种核苷酸变异,包括8个转变和1个转变。编码DNA区域内的两个A-G突变是非同义的,导致氨基酸的改变。古巴瘦素基因的基本局部比对搜索工具(BLAST)分析显示,与牛,山羊和绵羊的序列同源性为95-96%,而与其他农场动物物种的同源性则为86%至93%。 SSCP变体的序列分析显示内含子1内有一个单核苷酸多态性(SNP),变体'A'具有纯合的'T'等位基因,变体'B'具有纯合的'G'等位基因,而变体'C'具有杂合的'T /等位基因。 G'等位基因。发现已鉴定的SNP位点偏离Hardy-Weinberg平衡且杂合子的频率低于预期频率。该研究还发现外显子2内无变异,不利的等位基因'C'完全固定,据报道这与牛的牛奶和蛋白质产量降低有关

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