EMBO Reports · 2018 · 163 citations · 37 references
Life SciencesCell BiologyPhysiologyAutophagyMolecular PhysiologyPathophysiologyCellular RespirationMitochondrial Stress ResponsesMitophagyAutophagy ImpairmentAutophagy PathwayMitochondrial Degradation PathwaysMitochondrial FragmentationMitophagy CouplingMitophagy FluxMitophagy ImpairmentMitophagy Signaling
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.
37
Genome engineering using the CRISPR-Cas9 system
F. Ann Ran, Patrick D. Hsu, Jason Wright et al. · Nature Protocols · 2013 · 11.7K citations · Full text
The ubiquitin kinase PINK1 recruits autophagy receptors to induce mitophagy
Michael Lazarou, Danielle A. Sliter, Lesley A. Kane et al. · Nature · 2015 · 2.7K citations
Ubiquitin is phosphorylated by PINK1 to activate parkin
Fumika Koyano, Kei Okatsu, Hidetaka Kosako et al. · Nature · 2014 · 1.5K citations