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Abstract
Lifespan is an integrative phenotype whose genetic architecture is likely to highlight multiple processes with high impact on health and aging. Here, we conduct a genetic meta-analysis of longevity in Diversity Outbred (DO) mice that includes 2,444 animals from three independently conducted lifespan studies. We identify six loci that contribute significantly to lifespan independently of diet and drug treatment, one of which also influences lifespan in a sex-dependent manner, as well as an additional locus with a diet-specific effect on lifespan. Collectively, these loci explain over half of the estimated heritable variation in lifespan across these studies and provide insight into the genetic architecture of lifespan in DO mice.
Competing Interest Statement
This work was partially funded by Calico Life Sciences LLC. MNM, KMW, AR, ADF, and JGR were employees of Calico Life Sciences LLC at the time the study was conducted.
Footnotes
* Fixing a small problem with the pdf conversion.
* https://doi.org/10.5061/dryad.pnvx0k6z8
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