Center for Genetic Epidemiology, Department of Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA.
Istituto di Ricerca Genetica e Biomedica, Consiglio Nazionale delle Ricerche, Monserrato 09042, Cagliari, Italy.
Am J Hum Genet. 2020 Jul 2;107(1):60-71. doi: 10.1016/j.ajhg.2020.05.014. Epub 2020 Jun 12.
Adult height is one of the earliest putative examples of polygenic adaptation in humans. However, this conclusion was recently challenged because residual uncorrected stratification from large-scale consortium studies was considered responsible for the previously noted genetic difference. It thus remains an open question whether height loci exhibit signals of polygenic adaptation in any human population. We re-examined this question, focusing on one of the shortest European populations, the Sardinians, in addition to mainland European populations. We utilized height-associated loci from the Biobank Japan (BBJ) dataset to further alleviate concerns of biased ascertainment of GWAS loci and showed that the Sardinians remain significantly shorter than expected under neutrality (∼0.22 standard deviation shorter than Utah residents with ancestry from northern and western Europe [CEU] on the basis of polygenic height scores, p = 3.89 × 10). We also found the trajectory of polygenic height scores between the Sardinian and the British populations diverged over at least the last 10,000 years (p = 0.0082), consistent with a signature of polygenic adaptation driven primarily by the Sardinian population. Although the polygenic score-based analysis showed a much subtler signature in mainland European populations, we found a clear and robust adaptive signature in the UK population by using a haplotype-based statistic, the trait singleton density score (tSDS), driven by the height-increasing alleles (p = 9.1 × 10). In summary, by ascertaining height loci in a distant East Asian population, we further supported the evidence of polygenic adaptation at height-associated loci among the Sardinians. In mainland Europeans, the adaptive signature was detected in haplotype-based analysis but not in polygenic score-based analysis.
成人身高是人类多基因适应的最早例证之一。然而,最近这一结论受到了挑战,因为大型联盟研究中的未校正的剩余分层被认为是导致先前注意到的遗传差异的原因。因此,身高相关基因座在任何人类群体中是否表现出多基因适应的信号仍然是一个悬而未决的问题。我们重新研究了这个问题,除了欧洲大陆人群外,还重点关注了最短的欧洲人群之一——撒丁岛人。我们利用日本生物银行(BBJ)数据集的身高相关基因座,进一步减轻了对全基因组关联研究(GWAS)基因座偏倚确定的担忧,并表明撒丁岛人在中性条件下仍然明显比预期的矮(根据多基因身高得分,撒丁岛人与来自北欧和西欧的犹他州居民相比,短了约 0.22 个标准差[CEU],p=3.89×10)。我们还发现,撒丁岛人和英国人群之间的多基因身高得分轨迹在过去至少 10000 年发生了分歧(p=0.0082),这与主要由撒丁岛人驱动的多基因适应特征一致。尽管基于多基因评分的分析在欧洲大陆人群中显示出更为微妙的特征,但我们通过使用单倍型为基础的统计量,即特征单体密度得分(tSDS),在英国人群中发现了一个清晰而稳健的适应性特征,该特征由增加身高的等位基因驱动(p=9.1×10)。总之,通过在遥远的东亚人群中确定身高基因座,我们进一步支持了撒丁岛人身高相关基因座多基因适应的证据。在欧洲大陆人群中,适应性特征在单倍型分析中被检测到,但在多基因评分分析中没有被检测到。