Autophagy inhibition compromises degradation of ubiquitin-proteasome pathway substrates

Mol Cell. 2009 Feb 27;33(4):517-27. doi: 10.1016/j.molcel.2009.01.021.

Abstract

The two main routes that cells use for degrading intracellular proteins are the ubiquitin-proteasome and autophagy-lysosome pathways, which have been thought to have largely distinct clients. Here, we show that autophagy inhibition increases levels of proteasome substrates. This is largely due to p62 (also called A170/SQSTM1) accumulation after autophagy inhibition. Excess p62 inhibits the clearance of ubiquitinated proteins destined for proteasomal degradation by delaying their delivery to the proteasome's proteases. Our data show that autophagy inhibition, which was previously believed to only affect long-lived proteins, will also compromise the ubiquitin-proteasome system. This will lead to increased levels of short-lived regulatory proteins, like p53, as well as the accumulation of aggregation-prone proteins, with predicted deleterious consequences.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Autophagy*
  • Autophagy-Related Protein 5
  • Cell Line, Tumor
  • HeLa Cells
  • Humans
  • Mice
  • Microtubule-Associated Proteins / metabolism
  • Proteasome Endopeptidase Complex / metabolism*
  • RNA-Binding Proteins / metabolism
  • Transfection
  • Tumor Suppressor Protein p53 / metabolism
  • Ubiquitin / metabolism*

Substances

  • ATG5 protein, human
  • Autophagy-Related Protein 5
  • Microtubule-Associated Proteins
  • RNA-Binding Proteins
  • Tumor Suppressor Protein p53
  • Ubiquitin
  • Proteasome Endopeptidase Complex