Calico Life Sciences LLC. 1170 Veterans Blvd, South San Francisco 94080.
Ancestry, San Francisco, California 94107, and.
G3 (Bethesda). 2019 Sep 4;9(9):2863-2878. doi: 10.1534/g3.119.400448.
We present a massive investigation into the genetic basis of human lifespan. Beginning with a genome-wide association (GWA) study using a de-identified snapshot of the unique database - more than 300,000 genotyped individuals linked to pedigrees of over 400,000,000 people - we mapped six genome-wide significant loci associated with parental lifespan. We compared these results to a GWA analysis of the traditional lifespan proxy trait, age, and found only one locus, , to be associated with both age and lifespan. By combining the results with those of an independent UK Biobank dataset, we conducted a meta-analysis of more than 650,000 individuals and identified fifteen parental lifespan-associated loci. Beyond just those significant loci, our genome-wide set of polymorphisms accounts for up to 8% of the variance in human lifespan; this value represents a large fraction of the heritability estimated from phenotypic correlations between relatives.
我们对人类寿命的遗传基础进行了大规模的研究。从使用独特的数据库的匿名快照进行全基因组关联(GWA)研究开始 - 超过 30 万名个体被基因分型,并与超过 4 亿人的家系相关联 - 我们绘制了与父母寿命相关的六个全基因组显著位点。我们将这些结果与传统寿命代理特征年龄的 GWA 分析进行了比较,发现只有一个位点,与年龄和寿命都相关。通过将这些结果与独立的英国生物银行数据集相结合,我们对超过 65 万名个体进行了荟萃分析,确定了 15 个与父母寿命相关的位点。除了这些显著的位点之外,我们全基因组范围内的多态性可以解释人类寿命变异的 8%;这个值代表了从亲属之间表型相关性估计的遗传力的很大一部分。