Genetic modulation of hormone levels and life span in hybrids between laboratory and wild-derived mice

James M. Harper, Stephen J. Durkee, Robert C. Dysko, Steven N. Austad, Richard A. Miller

Research output: Contribution to journalArticle

35 Scopus citations


Previously we showed that mouse stocks derived from wild-caught progenitors are long-lived relative to genetically heterogeneous mice derived from laboratory-adapted strains. Here we replicate this life-span effect, and show that F2 hybrids between wild-derived and laboratory-derived stocks have intermediate survival patterns. Moreover, wild-derived mice are small, lean, and slow to mature, and have low serum insulin-like growth factor-I (IGF-I) relative to genet-ically heterogeneous mice. These traits, too, were at intermediate levels in the F2 hybrids. Furthermore, serum IGF-I at 6 months was a significant predictor of life span in two different populations of F2 hybrid mice. Pooling across stocks, life span was negatively correlated with body weight and serum IGF-I levels, and positively correlated with age at vaginal patency and serum leptin levels. Overall, these finding suggest that wild-derived mice harbor alleles that increase longevity, perhaps through effects on growth, maturation, and early-life hormone levels.

Original languageEnglish (US)
Pages (from-to)1019-1029
Number of pages11
JournalJournals of Gerontology - Series A Biological Sciences and Medical Sciences
Issue number10
StatePublished - Oct 2006


ASJC Scopus subject areas

  • Aging
  • Geriatrics and Gerontology

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