首页> 美国卫生研究院文献>PLoS Clinical Trials >No Evidence for Strong Recent Positive Selection Favoring the 7 Repeat Allele of VNTR in the DRD4 Gene
【2h】

No Evidence for Strong Recent Positive Selection Favoring the 7 Repeat Allele of VNTR in the DRD4 Gene

机译:没有证据表明最近的强阳性选择有利于DRD4基因中VNTR的7个重复等位基因

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。
获取外文期刊封面目录资料

摘要

The human dopamine receptor D4 (DRD4) gene contains a 48-bp variable number of tandem repeat (VNTR) in exon 3, encoding the third intracellular loop of this dopamine receptor. The DRD4 7R allele, which seems to have a single origin, is commonly observed in various human populations and the nucleotide diversity of the DRD4 7R haplotype at the DRD4 locus is reduced compared to the most common DRD4 4R haplotype. Based on these observations, previous studies have hypothesized that positive selection has acted on the DRD4 7R allele. However, the degrees of linkage disequilibrium (LD) of the DRD4 7R allele with single nucleotide polymorphisms (SNPs) outside the DRD4 locus have not been evaluated. In this study, to re-examine the possibility of recent positive selection favoring the DRD4 7R allele, we genotyped HapMap subjects for DRD4 VNTR, and conducted several neutrality tests including long range haplotype test and iHS test based on the extended haplotype homozygosity. Our results indicated that LD of the DRD4 7R allele was not extended compared to SNP alleles with the similar frequency. Thus, we conclude that the DRD4 7R allele has not been subjected to strong recent positive selection.
机译:人多巴胺受体D4(DRD4)基因在外显子3中包含48 bp可变数目的串联重复序列(VNTR),编码该多巴胺受体的第三个细胞内环。 DRD4 7R等位基因似乎具有单一起源,通常在各种人群中观察到,与最常见的DRD4 4R单倍型相比,DRD4 7R单倍型在DRD4位点的核苷酸多样性降低了。基于这些观察,先前的研究假设正选择作用于DRD4 7R等位基因。但是,尚未评估DRD4 7R外源具有单核苷酸多态性(SNP)的DRD4 7R等位基因的连锁不平衡(LD)程度。在这项研究中,为了重新检查有利于DRD4 7R等位基因的近期阳性选择的可能性,我们对HapMap受试者的DRD4 VNTR进行了基因分型,并基于扩展的单倍型纯合性进行了多种中性测试,包括远程单倍型测试和iHS测试。我们的结果表明,与具有相似频率的SNP等位基因相比,DRD4 7R等位基因的LD没有延伸。因此,我们得出结论,DRD4 7R等位基因尚未受到强烈的近期积极选择。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号