首页> 美国卫生研究院文献>PLoS Genetics >Transcriptome Sequencing from Diverse Human Populations Reveals Differentiated Regulatory Architecture
【2h】

Transcriptome Sequencing from Diverse Human Populations Reveals Differentiated Regulatory Architecture

机译:来自不同人群的转录组测序揭示了差异化的监管体系结构。

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

Large-scale sequencing efforts have documented extensive genetic variation within the human genome. However, our understanding of the origins, global distribution, and functional consequences of this variation is far from complete. While regulatory variation influencing gene expression has been studied within a handful of populations, the breadth of transcriptome differences across diverse human populations has not been systematically analyzed. To better understand the spectrum of gene expression variation, alternative splicing, and the population genetics of regulatory variation in humans, we have sequenced the genomes, exomes, and transcriptomes of EBV transformed lymphoblastoid cell lines derived from 45 individuals in the Human Genome Diversity Panel (HGDP). The populations sampled span the geographic breadth of human migration history and include Namibian San, Mbuti Pygmies of the Democratic Republic of Congo, Algerian Mozabites, Pathan of Pakistan, Cambodians of East Asia, Yakut of Siberia, and Mayans of Mexico. We discover that approximately 25.0% of the variation in gene expression found amongst individuals can be attributed to population differences. However, we find few genes that are systematically differentially expressed among populations. Of this population-specific variation, 75.5% is due to expression rather than splicing variability, and we find few genes with strong evidence for differential splicing across populations. Allelic expression analyses indicate that previously mapped common regulatory variants identified in eight populations from the International Haplotype Map Phase 3 project have similar effects in our seven sampled HGDP populations, suggesting that the cellular effects of common variants are shared across diverse populations. Together, these results provide a resource for studies analyzing functional differences across populations by estimating the degree of shared gene expression, alternative splicing, and regulatory genetics across populations from the broadest points of human migration history yet sampled.
机译:大规模测序工作已证明人类基因组内广泛的遗传变异。但是,我们对这种变化的起源,全球分布和功能后果的了解还远远不够。虽然已经在少数人群中研究了影响基因表达的调控变异,但尚未系统分析跨不同人群的转录组差异的广度。为了更好地了解人类中基因表达变异的谱图,可变剪接以及调节变异的群体遗传学,我们在人类基因组多样性小组中对来自45个个体的EBV转化的淋巴母细胞样细胞系的基因组,外显子组和转录组进行了测序( HGDP)。抽样人口跨越了人类迁徙历史的地理范围,包括纳米比亚的圣人,刚果民主共和国的姆布蒂i格米人,阿尔及利亚的莫扎比人,巴基斯坦的帕坦,东亚的柬埔寨人,西伯利亚的雅库特和墨西哥的玛雅人。我们发现,在个体中发现的基因表达变异中大约25.0%可以归因于种群差异。但是,我们发现在人群之间系统差异表达的基因很少。在这一特定于人群的变异中,有75.5%是由于表达而不是剪接变异性造成的,而且我们发现很少有基因有力地证明整个人群之间存在差异性剪接。等位基因表达分析表明,在国际单倍型图谱第3期项目的8个种群中鉴定的先前定位的共同调控变异体在我们的7个采样的HGDP种群中具有相似的作用,表明共同变异体的细胞效应在不同种群之间共享。总之,这些结果为从人口迁移历史的最广泛点估计人群中共有的基因表达,替代剪接和调控遗传学的程度提供了资源,从而为研究人群之间的功能差异提供了研究资源。

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