Dietary restriction suppresses proteotoxicity and enhances longevity by an hsf-1-dependent mechanism in Caenorhabditis elegans

Aging Cell. 2008 Jun;7(3):394-404. doi: 10.1111/j.1474-9726.2008.00385.x. Epub 2008 Mar 10.


Dietary restriction increases lifespan and slows the onset of age-associated disease in organisms from yeast to mammals. In humans, several age-related diseases are associated with aberrant protein folding or aggregation, including neurodegenerative disorders such as Alzheimer's, Parkinson's, and Huntington's diseases. We report here that dietary restriction dramatically suppresses age-associated paralysis in three nematode models of proteotoxicity. Similar to its longevity-enhancing properties, dietary restriction protects against proteotoxicity by a mechanism distinct from reduced insulin/IGF-1-like signaling. Instead, the heat shock transcription factor, hsf-1, is required for enhanced thermotolerance, suppression of proteotoxicity, and lifespan extension by dietary restriction. These findings demonstrate that dietary restriction confers a general protective effect against proteotoxicity and promotes longevity by a mechanism involving hsf-1.

Publication types

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

MeSH terms

  • Animals
  • Caenorhabditis elegans / drug effects
  • Caenorhabditis elegans / genetics
  • Caenorhabditis elegans / metabolism*
  • Caenorhabditis elegans Proteins / drug effects
  • Caenorhabditis elegans Proteins / metabolism*
  • Caloric Restriction*
  • Food Deprivation / physiology
  • Longevity / drug effects
  • Longevity / physiology*
  • Peptides / pharmacology
  • Transcription Factors / drug effects
  • Transcription Factors / metabolism*


  • Caenorhabditis elegans Proteins
  • Peptides
  • Transcription Factors
  • heat shock factor-1, C elegans
  • polyglutamine