Molecular signatures of longevity: Insights from cross-species comparative studies

Semin Cell Dev Biol. 2017 Oct;70:190-203. doi: 10.1016/j.semcdb.2017.08.007. Epub 2017 Aug 8.


Much of the current research on longevity focuses on the aging process within a single species. Several molecular players (e.g. IGF1 and MTOR), pharmacological compounds (e.g. rapamycin and metformin), and dietary approaches (e.g. calorie restriction and methionine restriction) have been shown to be important in regulating and modestly extending lifespan in model organisms. On the other hand, natural lifespan varies much more significantly across species. Within mammals alone, maximum lifespan differs more than 100 fold, but the underlying regulatory mechanisms remain poorly understood. Recent comparative studies are beginning to shed light on the molecular signatures associated with exceptional longevity. These include genome sequencing of microbats, naked mole rat, blind mole rat, bowhead whale and African turquoise killifish, and comparative analyses of gene expression, metabolites, lipids and ions across multiple mammalian species. Together, they point towards several putative strategies for lifespan regulation and cancer resistance, as well as the pathways and metabolites associated with longevity variation. In particular, longevity may be achieved by both lineage-specific adaptations and common mechanisms that apply across the species. Comparing the resulting cross-species molecular signatures with the within-species lifespan extension strategies will improve our understanding of mechanisms of longevity control and provide a starting point for novel and effective interventions.

Publication types

  • Comparative Study
  • Review
  • Research Support, Non-U.S. Gov't
  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Bowhead Whale / genetics
  • Bowhead Whale / growth & development
  • Bowhead Whale / metabolism
  • Caloric Restriction
  • Chiroptera / genetics
  • Chiroptera / growth & development
  • Chiroptera / metabolism
  • Gene Expression Regulation, Developmental*
  • Genome*
  • Humans
  • Insulin-Like Growth Factor I / genetics
  • Insulin-Like Growth Factor I / metabolism
  • Killifishes / genetics
  • Killifishes / growth & development
  • Killifishes / metabolism
  • Longevity / drug effects
  • Longevity / genetics*
  • Metabolome*
  • Metformin / pharmacology
  • Methionine / deficiency
  • Mole Rats / genetics
  • Mole Rats / growth & development
  • Mole Rats / metabolism
  • Sirolimus / pharmacology
  • TOR Serine-Threonine Kinases / genetics
  • TOR Serine-Threonine Kinases / metabolism
  • Transcriptome*


  • Insulin-Like Growth Factor I
  • Metformin
  • Methionine
  • TOR Serine-Threonine Kinases
  • Sirolimus