Characterization of a life-extending mutation in age-2, a new aging gene in Caenorhabditis elegans

J Gerontol A Biol Sci Med Sci. 1999 Apr;54(4):B137-42. doi: 10.1093/gerona/54.4.b137.

Abstract

We have generated a life-extending mutation, yw23, in Caenorhabditis elegans. The mutation is in what appears to be a new aging gene, which we have designated age-2. When homozygous, yw23 produces an increase of mean and maximum life span of about 20% over that of the wild-type strain, N2. Strain HG23 [age-2(yw23)] was obtained by screening for longer life spans among 430 lines of nematodes two generations after exposure to the mutagen ethylmethanesulfonate. Strain HG231 [age-2(yw23)] was obtained after a single out-crossing of HG23 to N2. When compared with N2, HG231 exhibits normal motility, slightly higher swimming rates, reduced fertility (especially at higher temperatures), somewhat longer development times, and a slightly larger size at the time of first egg laying. A Gompertz analysis suggests that HG231 extends life span by reducing the initial mortality rate. In genetic crosses, yw23 complements other known aging mutants in C. elegans genes-age-1, daf-2, spe-26, clk-1, clk-2, clk-3, and gro-1. A double-mutant strain, HG284, combining mutations in age-1 and age-2, lives longer than animals with individual mutations in either age-1 or age-2, and exhibits a longer life span at 25 degrees C than at 20 degrees C.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging / genetics*
  • Animals
  • Caenorhabditis elegans / genetics*
  • Caenorhabditis elegans / growth & development
  • Caenorhabditis elegans / physiology
  • Caenorhabditis elegans Proteins*
  • Chemotactic Factors / genetics
  • Crosses, Genetic
  • Cytoskeletal Proteins / genetics
  • Ethyl Methanesulfonate / pharmacology
  • Fertility
  • Genes, Recessive / genetics
  • Growth Substances / genetics
  • Helminth Proteins / genetics
  • Homozygote
  • Life Expectancy
  • Locomotion
  • Longevity / genetics*
  • Movement
  • Mutagens / pharmacology
  • Mutation / genetics*
  • Phosphatidylinositol 3-Kinases / genetics
  • Receptor, Insulin / genetics

Substances

  • CLK-1 protein, C elegans
  • Caenorhabditis elegans Proteins
  • Chemotactic Factors
  • Cytoskeletal Proteins
  • Growth Substances
  • Helminth Proteins
  • Mutagens
  • Spe-26 protein, C elegans
  • Ethyl Methanesulfonate
  • Phosphatidylinositol 3-Kinases
  • AGE-1 protein, C elegans
  • DAF-2 protein, C elegans
  • Receptor, Insulin