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 PMID:39368088  

High-content phenotypic analysis of a C. elegans recombinant inbred population identifies genetic and molecular regulators of lifespan.

Arwen W Gao | Gaby El Alam | Yunyun Zhu | Weisha Li | Jonathan Sulc | Xiaoxu Li | Elena Katsyuba | Terytty Y Li | Katherine A Overmyer | Amelia Lalou | Laurent Mouchiroud | Maroun Bou Sleiman | Matteo Cornaglia | Jean-David Morel | Riekelt H Houtkooper | Joshua J Coon | Johan Auwerx
Cell reports | 2024

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 C. elegans recombinant inbred advanced intercross 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 correlated positively with developmental time. We validated three longevity modulators, including rict-1, gfm-1, and mltn-1, among the top candidates obtained from multiomics data integration and quantitative trait locus (QTL) mapping. We translated their relevance to humans using UK Biobank data and showed that variants in GFM1 are associated with an elevated risk of age-related heart failure. We organized our dataset as a resource that allows interactive explorations for new longevity targets.

Pubmed ID: 39368088

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Associated grants

  • Agency: NIGMS NIH HHS, United States
    Id: P41 GM108538
  • Agency: NIGMS NIH HHS, United States
    Id: R35 GM118110

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