4.8 Article

The African Turquoise Killifish Genome Provides Insights into Evolution and Genetic Architecture of Lifespan

Journal

CELL
Volume 163, Issue 6, Pages 1539-1554

Publisher

CELL PRESS
DOI: 10.1016/j.cell.2015.11.008

Keywords

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Funding

  1. NIH [DP1AG044848]
  2. Glenn Laboratories for the Biology of Aging
  3. Max Planck Society
  4. Max Planck Institute for Biology of Ageing
  5. Dean's fellowship at Stanford and NIH [K99AG049934]
  6. Stanford Center for Computational Evolutionary and Human Genomics fellowship
  7. Life Sciences Research Foundation fellowship
  8. Damon Runyon fellowship
  9. Rothschild fellowship
  10. HFSP fellowship
  11. German Federal Ministry of Education and Research

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Lifespan is a remarkably diverse trait ranging from a few days to several hundred years in nature, but the mechanisms underlying the evolution of lifespan differences remain elusive. Here we de novo assemble a reference genome for the naturally short-lived African turquoise killifish, providing a unique resource for comparative and experimental genomics. The identification of genes under positive selection in this fish reveals potential candidates to explain its compressed lifespan. Several aging genes are under positive selection in this short-lived fish and long-lived species, raising the intriguing possibility that the same gene could underlie evolution of both compressed and extended lifespans. Comparative genomics and linkage analysis identify candidate genes associated with lifespan differences between various turquoise killifish strains. Remarkably, these genes are clustered on the sex chromosome, suggesting that short lifespan might have co-evolved with sex determination. Our study provides insights into the evolutionary forces that shape lifespan in nature.

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