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Detection of human adaptation during the past 2000 years

机译:在过去2000年中发现人类适应

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摘要

Detection of recent natural selection is a challenging problem in population genetics. Here we introduce the singleton density score (SDS), a method to infer very recent changes in allele frequencies from contemporary genome sequences. Applied to data from the UK10K Project, SDS reflects allele frequency changes in the ancestors of modern Britons during the past similar to 2000 to 3000 years. We see strong signals of selection at lactase and the major histocompatibility complex, and in favor of blond hair and blue eyes. For polygenic adaptation, we find that recent selection for increased height has driven allele frequency shifts across most of the genome. Moreover, we identify shifts associated with other complex traits, suggesting that polygenic adaptation has played a pervasive role in shaping genotypic and phenotypic variation in modern humans.
机译:最近的自然选择的检测是人口遗传学中一个具有挑战性的问题。在这里,我们介绍单重密度评分(SDS),一种从当代基因组序列中推断等位基因频率最近变化的方法。 SDS应用于UK10K项目的数据,反映了过去2000到3000年间现代英国人祖先的等位基因频率变化。我们在乳糖酶和主要的组织相容性复合体上看到了强烈的选择信号,并倾向于金色的头发和蓝色的眼睛。对于多基因适应,我们发现最近对高度增加的选择已经驱动了大多数基因组中的等位基因频移。此外,我们发现与其他复杂性状相关的变化,表明多基因适应已在塑造现代人类的基因型和表型变异中发挥了普遍作用。

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  • 来源
    《Science》 |2016年第6313期|760-764|共5页
  • 作者单位

    Stanford Univ, Dept Genet, Stanford, CA 94305 USA|Stanford Univ, Howard Hughes Med Inst, Stanford, CA 94305 USA;

    Stanford Univ, Dept Genet, Stanford, CA 94305 USA;

    Stanford Univ, Program Biomed Informat, Stanford, CA 94305 USA;

    Stanford Univ, Dept Genet, Stanford, CA 94305 USA|Stanford Univ, Howard Hughes Med Inst, Stanford, CA 94305 USA;

    Stanford Univ, Dept Genet, Stanford, CA 94305 USA|Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford, England|Univ Oxford, Oxford Ctr Diabet Endocrinol & Metab, Oxford, England;

    Stanford Univ, Dept Genet, Stanford, CA 94305 USA;

    Univ Lille, CNRS, Inst Pasteur Lille, UMR EGID 8199, F-59000 Lille, France|Univ Queensland, Inst Mol Biosci, Brisbane, Qld, Australia;

    Univ Lille, CNRS, Inst Pasteur Lille, UMR EGID 8199, F-59000 Lille, France;

    Univ Lille, CNRS, Inst Pasteur Lille, UMR EGID 8199, F-59000 Lille, France|Imperial Coll, Dept Genom Common Dis, London Hammersmith Hosp, London, England;

    Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford, England|Univ Oxford, Oxford Ctr Diabet Endocrinol & Metab, Oxford, England;

    Stanford Univ, Dept Genet, Stanford, CA 94305 USA|Stanford Univ, Howard Hughes Med Inst, Stanford, CA 94305 USA|Stanford Univ, Dept Biol, Stanford, CA 94305 USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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  • 入库时间 2022-08-18 02:51:47

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