Global Landscape and Dynamics of Parkin and USP30-dependent ubiquitylomes in iNeurons during mitophagic signaling
Details
Publication Year 2020-03-05,Volume 77,Issue #5,Page 1124-1142 e10
Journal Title
Molecular Cell
Publication Type
Journal Article
Abstract
The ubiquitin ligase Parkin, protein kinase PINK1, USP30 deubiquitylase, and p97 segregase function together to regulate turnover of damaged mitochondria via mitophagy, but our mechanistic understanding in neurons is limited. Here, we combine induced neurons (iNeurons) derived from embryonic stem cells with quantitative proteomics to reveal the dynamics and specificity of Parkin-dependent ubiquitylation under endogenous expression conditions. Targets showing elevated ubiquitylation in USP30(-/-) iNeurons are concentrated in components of the mitochondrial translocon, and the ubiquitylation kinetics of the vast majority of Parkin targets are unaffected, correlating with a modest kinetic acceleration in accumulation of pS65-Ub and mitophagic flux upon mitochondrial depolarization without USP30. Basally, ubiquitylated translocon import substrates accumulate, suggesting a quality control function for USP30. p97 was dispensable for Parkin ligase activity in iNeurons. This work provides an unprecedented quantitative landscape of the Parkin-modified ubiquitylome in iNeurons and reveals the underlying specificity of central regulatory elements in the pathway.
Publisher
Cell Press
Research Division(s)
Ubiquitin Signalling
PubMed ID
32142685
Terms of Use/Rights Notice
Refer to copyright notice on published article.


Creation Date: 2020-03-24 01:39:42
Last Modified: 2020-03-24 02:23:38
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