Dual role of USP30 in controlling basal pexophagy and mitophagy

被引:129
作者
Marcassa, Elena [1 ]
Kallinos, Andreas [1 ]
Jardine, Jane [1 ]
Rusilowicz-Jones, Emma V. [1 ]
Martinez, Aitor [1 ]
Kuehl, Sandra [2 ]
Islinger, Markus [2 ]
Clague, Michael J. [1 ]
Urbe, Sylvie [1 ]
机构
[1] Univ Liverpool, Inst Translat Med, Cellular & Mol Physiol, Liverpool, Merseyside, England
[2] Heidelberg Univ, Med Fac Mannheim, Inst Neuroanat, Ctr Biomed & Med Technol Mannheim, Mannheim, Germany
基金
英国医学研究理事会;
关键词
mitochondria; peroxisomes; PINK1; ubiquitin; mitophagy; USP30; RAT-LIVER; UBIQUITIN; PARKIN; MITOCHONDRIAL; PEROXISOMES; PINK1; PHOSPHORYLATION; PROTEIN; CHAINS; AUTOPHAGY;
D O I
10.15252/embr.201745595
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页数:14
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