Dual role of USP30 in controlling basal pexophagy and mitophagy

EMBO Rep. 2018 Jul;19(7):e45595. doi: 10.15252/embr.201745595. Epub 2018 Jun 12.

Abstract

USP30 is an integral protein of the outer mitochondrial membrane that counteracts PINK1 and Parkin-dependent mitophagy following acute mitochondrial depolarisation. Here, we use two distinct mitophagy reporter systems to reveal tonic suppression by USP30, of a PINK1-dependent component of basal mitophagy in cells lacking detectable Parkin. We propose that USP30 acts upstream of PINK1 through modulation of PINK1-substrate availability and thereby determines the potential for mitophagy initiation. We further show that a fraction of endogenous USP30 is independently targeted to peroxisomes where it regulates basal pexophagy in a PINK1- and Parkin-independent manner. Thus, we reveal a critical role of USP30 in the clearance of the two major sources of ROS in mammalian cells and in the regulation of both a PINK1-dependent and a PINK1-independent selective autophagy pathway.

Keywords: PINK1; USP30; mitochondria; mitophagy; peroxisomes; ubiquitin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Autophagy / genetics
  • Cell Line
  • Humans
  • Mitochondria / genetics
  • Mitochondrial Proteins / genetics*
  • Mitophagy / genetics*
  • Peroxisomes / genetics
  • Peroxisomes / metabolism
  • Protein Kinases / genetics*
  • Reactive Oxygen Species / metabolism
  • Thiolester Hydrolases / genetics*
  • Ubiquitin-Protein Ligases / genetics*

Substances

  • Mitochondrial Proteins
  • Reactive Oxygen Species
  • Usp30 protein, human
  • Ubiquitin-Protein Ligases
  • parkin protein
  • Protein Kinases
  • PTEN-induced putative kinase
  • Thiolester Hydrolases