MSTN gene polymo'/> Analysis of the single-nucleotide polymorphism in the 5'UTR and part of intron I of the sheep <i>MSTN</i> gene.
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Analysis of the single-nucleotide polymorphism in the 5'UTR and part of intron I of the sheep MSTN gene.

机译:绵羊 MSTN 基因5'UTR和部分内含子I的单核苷酸多态性分析。

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摘要

The myostatin (MSTN) gene region encompassing the 5'UTR and part of intron I was sequenced in animals of two herds of Latvian Darkhead sheep to extend data on the ovine MSTN gene polymorphism and to provide information useful for local breed conservation. Two and four polymorphic loci were revealed in the 5'UTR and intron I. Four and five local haplotypes were constructed, respectively. The genotyping data obtained and that previously reported for the same genomic region were combined in one dataset for the haplotype analysis. Recombination events were detected between loci (c.-40, c.-37) in the 5'UTR and (c.373+18, c.373+101) and (c.373+101, c.373+241) in intron I. Single-nucleotide polymorphisms at c.373+249 and c.373+323 appear to be involved in the strong linkage (p<0.01). Linkage blocks (c.373+241, c.373+243) and (c.373+241, c.373+259) were revealed at nominal (p<0.05) level of probability. Haplotype-specific patterns of the transcription factor binding sites predicted in silico were constructed to evaluate a putative functional significance of the particular alleles and haplotypes. A nucleotide at c.373+18 was shown to influence the pre-mRNA secondary structure. DNA curvature predicted in silico for allele c.373+101C was proven experimentally. A possible impact of the particular polymorphisms on the transcription and/or splicing efficiency is discussed.
机译:在两个拉脱维亚黑头羊群的动物中对包含5'UTR和部分内含子I的肌生长抑制素( MSTN )基因区域进行了测序,以扩展绵羊 MSTN 基因的数据多态性,并为当地品种保护提供有用的信息。在5'UTR和内含子I中揭示了两个和四个多态位点。分别构建了四个和五个局部单倍型。将获得的基因分型数据和先前报告的同一基因组区域的基因分型数据合并到一个数据集中进行单倍型分析。在5'UTR的基因座(c.-40,c.-37)与(c.373 + 18,c.373 + 101)和(c.373 + 101,c.373 + 241)之间检测到重组事件c.373 + 249和c.373 + 323的单核苷酸多态性似乎与强连锁有关( p <0.01)。链接块(c.373 + 241,c.373 + 243)和(c.373 + 241,c.373 + 259)以标称( p <0.05)概率显示。构建了计算机模拟中预测的转录因子结合位点的单倍型特异性模式,以评估特定等位基因和单倍型的假定功能意义。已显示在c.373 + 18处的核苷酸会影响pre-mRNA的二级结构。实验证明了等位基因c.373 + 101C在计算机上预测的DNA曲率。讨论了特定多态性对转录和/或剪接效率的可能影响。

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