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Polymorphism analysis of six selenoprotein genes: support for a selective sweep at the glutathione peroxidase 1 locus (3p21) in Asian populations

机译:六个硒蛋白基因的多态性分析:支持亚洲人群谷胱甘肽过氧化物酶1基因座(3p21)的选择性扫描

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Background There are at least 25 human selenoproteins, each characterized by the incorporation of selenium into the primary sequence as the amino acid selenocysteine. Since many selenoproteins have antioxidant properties, it is plausible that inter-individual differences in selenoprotein expression or activity could influence risk for a range of complex diseases, such as cancer, infectious diseases as well as deleterious responses to oxidative stressors like cigarette smoke. To capture the common genetic variants for 6 important selenoprotein genes (GPX1, GPX2, GPX3, GPX4, TXNRD1, and SEPP1) known to contribute to antioxidant host defenses, a re-sequence analysis was conducted across these genes with particular interest directed at the coding regions, intron-exon borders and flanking untranslated regions (UTR) for each gene in an 102 individual population representative of 4 major ethnic groups found within the United States. Results For 5 of the genes there was no strong evidence for selection according to the expectations of the neutral equilibrium model of evolution; however, at the GPX1 locus (3p21) there was evidence for positive selection. Strong confirmatory evidence for recent positive selection at the genomic region 3p21 in Asian populations is provided by data from the International HapMap project. Conclusion The SNPs and fine haplotype maps described in this report will be valuable resources for future functional studies, for population specific genetic studies designed to comprehensively explore the role of selenoprotein genetic variants in the etiology of various human diseases, and to define the forces responsible for a recent selective sweep in the vicinity of the GPX1 locus.
机译:背景技术至少有25种人硒蛋白,每种蛋白的特征是将硒作为氨基酸硒代半胱氨酸掺入一级序列中。由于许多硒蛋白具有抗氧化特性,因此硒蛋白表达或活性的个体差异可能影响一系列复杂疾病的风险,例如癌症,传染病以及对氧化应激(如香烟烟雾)的有害反应。为了捕获已知有助于抗氧化剂宿主防御的6个重要硒蛋白基因(GPX1,GPX2,GPX3,GPX4,TXNRD1和SEPP1)的常见遗传变异,对这些基因进行了重新序列分析,尤其关注编码在美国境内发现的4个主要族裔的102个个体人口中,每个基因的区域,内含子-外显子边界和侧翼非翻译区(UTR)。结果对于其中的5个基因,没有足够的证据根据中性平衡进化模型的期望进行选择。但是,在GPX1位点(3p21),有证据表明存在阳性选择。国际HapMap项目提供的数据为近期在亚洲人群中3p21基因组区域的阳性选择提供了有力的确认证据。结论本报告中所述的SNP和精细的单倍型图谱将为将来的功能研究,特定人群的遗传研究提供宝贵资源,这些研究旨在全面探讨硒蛋白基因变异在各种人类疾病的病因中的作用,并确定引起疾病的力量。最近在GPX1基因座附近进行的选择性扫描。

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