The endogenous siRNA pathway in Drosophila impacts stress resistance and lifespan by regulating metabolic homeostasis

FEBS Lett. 2011 Oct 3;585(19):3079-85. doi: 10.1016/j.febslet.2011.08.034. Epub 2011 Aug 30.

Abstract

Small non-coding RNAs regulate gene expression in a sequence-specific manner. In Drosophila, Dicer-2 (Dcr-2) functions in the biogenesis of endogenous small interfering RNAs (endo-siRNAs). We identified 21 distinct proteins that exhibited a ≥ 1.5-fold change as a consequence of loss of dcr-2 function. Most of these were metabolic genes implicated in stress resistance and aging. dcr-2 Mutants had reduced lifespan and were hypersensitive to oxidative, endoplasmic reticulum, starvation, and cold stresses. Furthermore, loss of dcr-2 function led to abnormal lipid and carbohydrate metabolism. Our results suggest roles for the endo-siRNA pathway in metabolic regulation and defense against stress and aging in Drosophila.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Drosophila Proteins / genetics
  • Drosophila Proteins / metabolism
  • Drosophila melanogaster / physiology*
  • Energy Metabolism / genetics*
  • Female
  • Homeostasis / genetics*
  • Life Expectancy*
  • Male
  • RNA Helicases / genetics
  • RNA Helicases / metabolism
  • RNA Interference
  • RNA, Small Interfering / genetics
  • RNA, Small Interfering / metabolism*
  • Ribonuclease III / genetics
  • Ribonuclease III / metabolism
  • Stress, Physiological / genetics*

Substances

  • Drosophila Proteins
  • RNA, Small Interfering
  • DCR-2 protein, Drosophila
  • Dcr-1 protein, Drosophila
  • Ribonuclease III
  • RNA Helicases