Genetic variation and aging

James W Curtsinger, Hidenori H. Fukui, Aziz A. Khazaeli, Andrew Kirscher, Scott D. Pletcher, Daniel E.L. Promislow, Marc Tatar

Research output: Contribution to journalReview articlepeer-review

101 Scopus citations

Abstract

Life span is subject to genetic modification in yeasts, nematodes, fruit flies, mice, humans, and other vertebrates and invertebrates. There are a few single-gene mutants known that extend life span in yeast and nematodes; in other experimental systems the character is treated quantitatively, and generally has a low to moderate heritability. Life span responds to artificial selection in Drosophila and Caenorhabditis. There are many candidate genes presently under investigation, including the anti-oxidizing enzymes and heat-shock proteins. The main evolutionary models of senescence are antagonistic pleiotropy and mutation accumulation, neither of which has substantial experimental support. The incorporation of analytical techniques from demography is playing an increasing role in research on aging.

Original languageEnglish (US)
Pages (from-to)553-575
Number of pages23
JournalAnnual Review of Genetics
Volume29
DOIs
StatePublished - 1995

Keywords

  • candidate genes
  • demography
  • evolution of senescence
  • genetic variation
  • life span

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