Gao Arwen W, Alam Gaby El, Zhu Yunyun, Li Weisha, Katsyuba Elena, Sulc Jonathan, Li Terytty Y, Li Xiaoxu, Overmyer Katherine A, Lalou Amelia, Mouchiroud Laurent, Sleiman Maroun Bou, Cornaglia Matteo, Morel Jean-David, Houtkooper Riekelt H, Coon Joshua J, Auwerx Johan
Laboratory of Integrative Systems Physiology, Interfaculty Institute of Bioengineering, École Polytechnique Fédérale de Lausanne, CH-1015 Lausanne, Switzerland.
Laboratory Genetic Metabolic Diseases, Amsterdam Gastroenterology, Endocrinology, and Metabolism, Amsterdam UMC, University of Amsterdam, Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands.
bioRxiv. 2024 Jan 16:2024.01.15.575638. doi: 10.1101/2024.01.15.575638.
Lifespan is influenced by complex interactions between genetic and environmental factors. Studying those factors in model organisms of a single genetic background limits their translational value for humans. Here, we mapped lifespan determinants in 85 genetically diverse recombinant intercross advanced inbred lines (RIAILs). We assessed molecular profiles - transcriptome, proteome, and lipidome - and life-history traits, including lifespan, development, growth dynamics, and reproduction. RIAILs exhibited large variations in lifespan, which positively correlated with developmental time. Among the top candidates obtained from multi-omics data integration and QTL mapping, we validated known and novel longevity modulators, including , and . We translated their relevance to humans using UK Biobank data and showed that variants in and are associated with an elevated risk of age-related heart disease, dementia, diabetes, kidney, and liver diseases. We organized our dataset as a resource (https://lisp-lms.shinyapps.io/RIAILs/) that allows interactive explorations for new longevity targets.
寿命受到遗传和环境因素之间复杂相互作用的影响。在单一遗传背景的模式生物中研究这些因素限制了它们对人类的转化价值。在这里,我们在85个遗传多样化的重组杂交近交系(RIAILs)中绘制了寿命决定因素。我们评估了分子图谱——转录组、蛋白质组和脂质组——以及生命史特征,包括寿命、发育、生长动态和繁殖。RIAILs在寿命上表现出很大的差异,这与发育时间呈正相关。在从多组学数据整合和QTL定位获得的顶级候选基因中,我们验证了已知和新的长寿调节因子,包括 、 和 。我们使用英国生物银行的数据将它们与人类的相关性进行了转化,并表明 和 中的变异与年龄相关的心脏病、痴呆、糖尿病、肾脏和肝脏疾病的风险升高有关。我们将我们的数据集组织成一个资源(https://lisp-lms.shinyapps.io/RIAILs/),允许对新的长寿目标进行交互式探索。