Mullis Martin N, Wright Kevin M, Raj Anil, Gatti Daniel M, Reifsnyder Peter C, Flurkey Kevin, Archer Jonathan R, Robinson Laura, Di Francesco Andrea, Svenson Karen L, Korstanje Ron, Harrison David E, Ruby J Graham, Churchill Gary A
Calico Life Sciences LLC, 1170 Veterans Blvd, South San Francisco, CA 94080, United States.
The Jackson Laboratory, 600 Main St, Bar Harbor, ME 04609, United States.
Genetics. 2025 Aug 6;230(4). doi: 10.1093/genetics/iyaf081.
Lifespan is an integrative phenotype whose genetic architecture is likely to highlight multiple processes with high impact on health and aging. Here, we conducted a genetic mega-analysis of longevity in Diversity Outbred (DO) mice that included 2,444 animals from 3 independently conducted lifespan studies. We identified 8 loci that contributed significantly to lifespan independently of diet and drug treatment in at least one study. One of these loci also influenced lifespan in a sex-dependent manner, and we detected an additional locus with a diet-specific effect on lifespan. Collectively, these loci explained over half of the estimated heritable variation in lifespan across these studies and provided insight into the genetic architecture of lifespan in DO mice.
寿命是一种综合表型,其遗传结构可能突出了对健康和衰老有重大影响的多个过程。在这里,我们对多样性远交(DO)小鼠的寿命进行了一项基因荟萃分析,该分析纳入了来自3项独立进行的寿命研究的2444只动物。我们在至少一项研究中确定了8个位点,这些位点对寿命有显著贡献,且与饮食和药物治疗无关。其中一个位点还以性别依赖的方式影响寿命,并且我们检测到另一个对寿命有饮食特异性影响的位点。总体而言,这些位点解释了这些研究中估计的寿命遗传变异的一半以上,并为DO小鼠寿命的遗传结构提供了见解。