USP14 regulates autophagy by suppressing K63 ubiquitination of Beclin 1

Genes Dev. 2016 Aug 1;30(15):1718-30. doi: 10.1101/gad.285122.116.

Abstract

The ubiquitin-proteasome system (UPS) and autophagy are two major intracellular degradative mechanisms that mediate the turnover of complementary repertoires of intracellular proteomes. Simultaneously activating both UPS and autophagy might provide a powerful strategy for the clearance of misfolded proteins. However, it is not clear whether UPS and autophagy can be controlled by a common regulatory mechanism. K48 deubiquitination by USP14 is known to inhibit UPS. Here we show that USP14 regulates autophagy by negatively controlling K63 ubiquitination of Beclin 1. Furthermore, we show that activation of USP14 by Akt-mediated phosphorylation provides a mechanism for Akt to negatively regulate autophagy by promoting K63 deubiquitination. Our study suggests that Akt-regulated USP14 activity modulates both proteasomal degradation and autophagy through controlling K48 and K63 ubiquitination, respectively. Therefore, regulation of USP14 provides a mechanism for Akt to control both proteasomal and autophagic degradation. We propose that inhibition of USP14 may provide a strategy to promote both UPS and autophagy for developing novel therapeutics targeting neurodegenerative diseases.

Keywords: Akt; Beclin 1; USP14; autophagy.

MeSH terms

  • Autophagy / physiology*
  • Beclin-1 / metabolism*
  • Class III Phosphatidylinositol 3-Kinases / metabolism
  • Gene Expression
  • HEK293 Cells
  • Humans
  • Oncogene Protein v-akt / metabolism
  • Phosphorylation
  • Ubiquitin Thiolesterase / genetics
  • Ubiquitin Thiolesterase / metabolism*
  • Ubiquitination*

Substances

  • Beclin-1
  • USP14 protein, human
  • Class III Phosphatidylinositol 3-Kinases
  • Oncogene Protein v-akt
  • Ubiquitin Thiolesterase