首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Global landscape of recent inferred Darwinian selection for Homo sapiens
【2h】

Global landscape of recent inferred Darwinian selection for Homo sapiens

机译:最近推断的达尔文人选择智人的全球格局

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。

摘要

By using the 1.6 million single-nucleotide polymorphism (SNP) genotype data set from Perlegen Sciences [Hinds, D. A., Stuve, L. L., Nilsen, G. B., Halperin, E., Eskin, E., Ballinger, D. G., Frazer, K. A. & Cox, D. R. (2005) Science 307, 1072–1079], a probabilistic search for the landscape exhibited by positive Darwinian selection was conducted. By sorting each high-frequency allele by homozygosity, we search for the expected decay of adjacent SNP linkage disequilibrium (LD) at recently selected alleles, eliminating the need for inferring haplotype. We designate this approach the LD decay (LDD) test. By these criteria, 1.6% of Perlegen SNPs were found to exhibit the genetic architecture of selection. These results were confirmed on an independently generated data set of 1.0 million SNP genotypes (International Human Haplotype Map Phase I freeze). Simulation studies indicate that the LDD test, at the megabase scale used, effectively distinguishes selection from other causes of extensive LD, such as inversions, population bottlenecks, and admixture. The ≈1,800 genes identified by the LDD test were clustered according to Gene Ontology (GO) categories. Based on overrepresentation analysis, several predominant biological themes are common in these selected alleles, including host–pathogen interactions, reproduction, DNA metabolism/cell cycle, protein metabolism, and neuronal function.
机译:通过使用来自Perlegen Sciences的160万个单核苷酸多态性(SNP)基因型数据集[Hinds,DA,Stuve,LL,Nilsen,GB,Halperin,E.,Eskin,E.,Ballinger,DG,Frazer,KA&Cox ,DR(2005)Science 307,1072–1079],对由积极的达尔文式选择所展现的景观进行了概率搜索。通过按纯合性对每个高频等位基因进行排序,我们在最近选择的等位基因上搜索了相邻SNP连锁不平衡(LD)的预期衰减,从而无需推断单倍型。我们将这种方法指定为LD衰减(LDD)测试。通过这些标准,发现有1.6%的Perlegen SNP具有选择的遗传结构。这些结果在一个独立生成的100万个SNP基因型数据集上得到了证实(国际人类单倍型图I期冻结)。模拟研究表明,在所使用的兆碱基规模下,LDD测试可以有效地将选择与广泛的LD的其他原因区分开,例如反转,人口瓶颈和混合。根据基因本体论(GO)类别,将通过LDD测试鉴定的约1800个基因聚类。基于超量表达分析,这些选定的等位基因中共有几个主要的生物学主题,包括宿主-病原体相互作用,繁殖,DNA代谢/细胞周期,蛋白质代谢和神经元功能。

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