bioRxiv · 10.1101/2020.06.02.129908
The burden of rare protein-truncating genetic variants on human lifespan
Abstract
Genetic predisposition is believed to contribute substantially to the age at which we die. Genome-wide association studies (GWAS) have implicated more than 20 genetic loci to phenotypes related to human lifespan1. However, little is known about how lifespan is impacted by gene loss-of-function. Through whole-exome sequencing of 238,239 UK Biobank participants, we assessed the relevance of protein-truncating variant (PTV) gene burden on individual and parental survival. We identified exome-wide (P<2.5e-6) significant associations between BRCA2, BRCA1, TET2, PPM1D, LDLR, EML2 and DEDD2 PTV-burden with human lifespan. Gene and gene-set PTV-burden phenome-wide association studies (PheWAS) further highlighted the roles of these genes in cancer and cardiovascular disease as relevant for overall survival. The overlap between PTV-burden and prior GWAS results was modest, underscoring the value of sequencing in well-powered cohorts to complement GWAS for identifying loci associated with complex traits and disease.
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Liu, J. Z., Chen, C.-Y., Tsai, E., Whelan, C. D., Sexton, D., John, S., Runz, H.. 2020-06-03. The burden of rare protein-truncating genetic variants on human lifespan. https://doi.org/10.1101/2020.06.02.129908
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