Department of Psychiatry, Yale University School of Medicine, West Haven, CT, 06516, USA.
VA CT Healthcare Center, West Haven, CT, 06516, USA.
BMC Biol. 2022 Nov 7;20(1):249. doi: 10.1186/s12915-022-01449-2.
Introgression from extinct Neanderthal and Denisovan human species has been shown to contribute to the genetic pool of modern human populations and their phenotypic spectrum. Evidence of how Neanderthal introgression shaped the genetics of human traits and diseases has been extensively studied in populations of European descent, with signatures of admixture reported for instance in genes associated with pigmentation, immunity, and metabolic traits. However, limited information is currently available about the impact of archaic introgression on other ancestry groups. Additionally, to date, no study has been conducted with respect to the impact of Denisovan introgression on the health and disease of modern populations. Here, we compare the way evolutionary pressures shaped the genetics of complex traits in East Asian and European populations, and provide evidence of the impact of Denisovan introgression on the health of East Asian and Central/South Asian populations.
Leveraging genome-wide association statistics from the Biobank Japan and UK Biobank, we assessed whether Denisovan and Neanderthal introgression together with other evolutionary genomic signatures were enriched for the heritability of physiological and pathological conditions in populations of East Asian and European descent. In EAS, Denisovan-introgressed loci were enriched for coronary artery disease heritability (1.69-fold enrichment, p=0.003). No enrichment for archaic introgression was observed in EUR. We also performed a phenome-wide association study of Denisovan and Neanderthal alleles in six ancestry groups available in the UK Biobank. In EAS, the Denisovan-introgressed SNP rs62391664 in the major histocompatibility complex region was associated with albumin/globulin ratio (beta=-0.17, p=3.57×10). Neanderthal-introgressed alleles were associated with psychiatric and cognitive traits in EAS (e.g., "No Bipolar or Depression"-rs79043717 beta=-1.5, p=1.1×10), and with blood biomarkers (e.g., alkaline phosphatase-rs11244089 beta=0.1, p=3.69×10) and red hair color (rs60733936 beta=-0.86, p=4.49×10) in EUR. In the other ancestry groups, Neanderthal alleles were associated with several traits, also including the use of certain medications (e.g., Central/South East Asia: indapamide - rs732632 beta=-2.38, p=5.22×10).
Our study provides novel evidence regarding the impact of archaic introgression on the genetics of complex traits in worldwide populations, highlighting the specific contribution of Denisovan introgression in EAS populations.
已证实灭绝的尼安德特人和丹尼索瓦人物种的基因渗入为现代人类群体及其表型谱的基因库做出了贡献。在欧洲血统的人群中,广泛研究了尼安德特人基因渗入如何塑造人类特征和疾病的遗传,例如在与色素沉着、免疫和代谢特征相关的基因中报告了混合的特征。然而,目前关于古老基因渗入对其他祖先群体的影响的信息有限。此外,迄今为止,尚无研究针对丹尼索瓦人基因渗入对现代人群健康和疾病的影响。在这里,我们比较了进化压力塑造东亚和欧洲人群复杂特征遗传的方式,并提供了丹尼索瓦人基因渗入对东亚和中/南亚人群健康影响的证据。
利用来自日本生物银行和英国生物银行的全基因组关联统计数据,我们评估了丹尼索瓦人和尼安德特人基因渗入以及其他进化基因组特征是否与东亚和欧洲血统人群的生理和病理状况的遗传力有关。在东亚人群中,丹尼索瓦人基因渗入的位点与冠心病遗传力呈富集趋势(1.69 倍富集,p=0.003)。在欧洲人群中,未观察到古老基因渗入的富集。我们还在英国生物银行中可获得的六个祖先群体中进行了丹尼索瓦人和尼安德特人等位基因的全表型关联研究。在东亚人群中,主要组织相容性复合体区域中的丹尼索瓦人基因渗入 SNP rs62391664 与白蛋白/球蛋白比值相关(β=-0.17,p=3.57×10)。尼安德特人基因渗入的等位基因与东亚人群的精神和认知特征有关(例如,“无双相或抑郁”-rs79043717 β=-1.5,p=1.1×10),并且与血液生物标志物(例如,碱性磷酸酶-rs11244089 β=0.1,p=3.69×10)和红头发颜色(rs60733936 β=-0.86,p=4.49×10)有关在欧洲人群中。在其他祖先群体中,尼安德特人等位基因与包括某些药物使用在内的多种特征有关(例如,中/东南亚:吲达帕胺-rs732632 β=-2.38,p=5.22×10)。
我们的研究提供了关于古老基因渗入对全球人群复杂特征遗传影响的新证据,强调了丹尼索瓦人基因渗入在东亚人群中的特定贡献。