Heat shock protein accumulation is upregulated in a long-lived mutant of Caenorhabditis elegans

J Gerontol A Biol Sci Med Sci. 2001 Jul;56(7):B281-7. doi: 10.1093/gerona/56.7.b281.

Abstract

We present evidence for elevated levels of heat shock protein 16 (HSP16) in an intrinsically thermotolerant, long-lived strain of Caenorhabditis elegans during and after heat stress. Mutation of the age-1 gene, encoding a phosphatidylinositol 3-kinase catalytic subunit, results in both extended life span (Age) and increased intrinsic thermotolerance (Itt) in adult hermaphrodites. We subjected age-synchronous cohorts of worms to lethal and nonlethal thermal stress and observed the accumulation of a small (16-18 kd) heat-shock-specific polypeptide detected by an antibody raised against C. elegans HSP16. Strains carrying the mutation hx546 consistently accumulated HSP16 to higher levels than a wild-type strain. Significantly, overaccumulation of HSP16 in the age-1(hx546) strain following heat was observed throughout the adult life span. A chimeric transgene containing the Escherichia coli beta-galactosidase gene fused to a C. elegans HSP16-41 transcriptional promoter was introduced into wild-type and age-1(hx546) backgrounds. Heat-inducible expression of the transgene was elevated in the age-1(hx546) strain compared with the wild-type strain under a wide variety of heat shock and recovery conditions. These observations are consistent with a model in which Age mutations exhibit thermotolerance and extended life span as a result of elevated levels of molecular chaperones.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aging / genetics*
  • Animals
  • Bacterial Proteins*
  • Caenorhabditis elegans / enzymology
  • Caenorhabditis elegans / genetics
  • Caenorhabditis elegans / metabolism*
  • Caenorhabditis elegans Proteins*
  • Escherichia coli / enzymology
  • Gene Transfer Techniques
  • Genes, Reporter / genetics
  • Heat-Shock Proteins / genetics
  • Heat-Shock Proteins / metabolism*
  • Hot Temperature*
  • Longevity
  • Molecular Chaperones / metabolism
  • Mutation*
  • Phosphatidylinositol 3-Kinases / genetics
  • Promoter Regions, Genetic / genetics
  • Recombinant Fusion Proteins
  • Time Factors
  • Transcription, Genetic
  • Transgenes / genetics
  • Up-Regulation
  • beta-Galactosidase / genetics

Substances

  • Bacterial Proteins
  • Caenorhabditis elegans Proteins
  • Heat-Shock Proteins
  • HspA protein, bacteria
  • Molecular Chaperones
  • Recombinant Fusion Proteins
  • beta-Galactosidase