Format

Send to

Choose Destination
Commun Integr Biol. 2014 Jun 13;7:e29483. doi: 10.4161/cib.29483. eCollection 2014.

Analysis of the Retromer complex-WASH complex interaction illuminates new avenues to explore in Parkinson disease.

Author information

1
University of Cambridge; Cambridge Institute for Medical Research; Wellcome Trust/MRC Building; Addenbrookes Hospital; Cambridge UK.

Abstract

The retromer complex mediates endosomal protein sorting by concentrating membrane proteins (cargo) into nascent tubules formed through the action of sorting nexin (SNX) proteins. The WASH complex is recruited to endosomes by binding to the VPS35 subunit of retromer and facilitates cargo protein sorting by promoting formation of endosomally-localized F-actin. The VPS35 protein is mutated in Parkinson disease (PD) and a recent report has revealed that the PD-causing mutation impairs the association of retromer with the WASH complex leading to perturbed endosomal protein sorting. Another important player in endosomal protein sorting is the DNAJC13/RME-8 protein, which associates with SNX1 and has also recently been linked to PD. An additional recent report has now shown that RME-8 also interacts with the WASH complex thus establishing retromer and WASH complex-mediated endosomal protein sorting as a key pathway linked to the pathology of PD and providing new avenues to explore in the search for insights into the disease mechanism.

KEYWORDS:

Parkinson disease; RME-8; WASH complex; endosomal protein sorting; retromer; tubule

Supplemental Content

Full text links

Icon for Taylor & Francis Icon for PubMed Central
Loading ...
Support Center