Suppr超能文献

寿命的基因调控:动态效应、性别差异及体重权衡

Genetic Modulation of Lifespan: Dynamic Effects, Sex Differences, and Body Weight Trade-offs.

作者信息

Arends Danny, Ashbrook David G, Roy Suheeta, Lu Lu, Sloan Zachary, Centeno Arthur G, Lamour Kurt H, de Magalhães João Pedro, Prins Pjotr, Broman Karl W, Sen Saunak, Mitchell Sarah J, MacArthur Michael R, Akin Özlem Altintas, Auwerx Johan, Bajwa Amandeep, Diaz Vivian, Harrison David E, Strong Randy, Nelson James F, Mozhui Khyobeni, Williams Evan G, Miller Richard A, Williams Robert W

机构信息

Department of Applied Sciences, Northumbria University, Newcastle upon Tyne, UK.

Department of Genetics, Genomics and Informatics, University of Tennessee Health Science Center; Memphis, TN, USA.

出版信息

bioRxiv. 2025 Jul 21:2025.04.27.649857. doi: 10.1101/2025.04.27.649857.

Abstract

The dynamics of lifespan are shaped by DNA variants that exert effects at different ages. We have mapped genetic loci that modulate age-specific mortality using an actuarial approach. We started with an initial population of 6,438 pubescent siblings and ended with a survivorship of 559 mice that lived to at least 1100 days. Twenty-nine loci dynamically modulate the mean lifespan of survivorships with strong age- and sex-specific effects. Fourteen have relatively steady effects on mortality while other loci act forcefully only early or late in life and with polarities of effects that invert. A distinct set of 19 loci shape the correlation between weights of young adults with their life expectancies-much more strongly so in males than females. Another set of 11 loci shape the correlation between weights at older ages with life expectancies. The and loci share 289 age-dependent epistatic interactions (LODs ≥3.8) but fewer than 4% are common to both sexes. We provide two examples of how to move from maps toward potential mechanisms. Our findings provide an empirical bridge between evolutionary theories on aging and genetic and molecular causes. These loci and their interactions are key to begin to understand the impact of interventions that may extend healthy lifespan in mice and even in humans.

摘要

寿命动态受到在不同年龄发挥作用的DNA变异的影响。我们使用精算方法绘制了调节特定年龄死亡率的基因位点图谱。我们从6438只青春期同胞小鼠的初始群体开始,最终存活至至少1100天的小鼠有559只。29个基因位点动态调节存活小鼠的平均寿命,具有强烈的年龄和性别特异性效应。14个基因位点对死亡率有相对稳定的影响,而其他基因位点仅在生命早期或晚期有力地发挥作用,且效应极性相反。一组独特的19个基因位点塑造了年轻成年小鼠体重与其预期寿命之间的相关性——在雄性中比在雌性中更为强烈。另一组11个基因位点塑造了老年小鼠体重与预期寿命之间的相关性。这些基因位点共享289种年龄依赖性上位相互作用(LOD≥3.8),但两性共有的不到4%。我们提供了两个关于如何从图谱转向潜在机制的例子。我们的发现为衰老的进化理论与遗传和分子原因之间搭建了一座实证桥梁。这些基因位点及其相互作用是开始理解可能延长小鼠甚至人类健康寿命的干预措施影响的关键。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e64/12330653/f5806e850dc8/nihpp-2025.04.27.649857v2-f0007.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验