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The Parkinson’s disease protein LRRK2 interacts with the GARP complex to promote retrograde transport to the trans-Golgi network

Title: The Parkinson’s disease protein LRRK2 interacts with the GARP complex to promote retrograde transport to the trans-Golgi network
Authors: Beilina, A; Bonet-Ponce, L; Kumaran, R; Kordich, JJ; Ishida, M; Mamais, A; Kaganovich, A; Saez-Atienzar, S; Gershlick, DC; Roosen, DA; Pellegrini, L; Malkov, V; Fell, MJ; Harvey, K; Bonifacino, JS; Moore, DJ; Cookson, MR
Source: Cell Reports , 31 (5) , Article 107614. (2020)
Publisher Information: Elsevier
Publication Year: 2020
Collection: University College London: UCL Discovery
Subject Terms: Leucine-rich repeat kinase 2; neurodegeneration; membrane trafficking; lysosome; endosome; neurodegenerative disease; VPS52; RAB29; RAB7L1; neuroscience
Description: Mutations in Leucine-rich repeat kinase 2 (LRRK2) cause Parkinson’s disease (PD). However, the precise function of LRRK2 remains unclear. We report an interaction between LRRK2 and VPS52, a subunit of the Golgi-associated retrograde protein (GARP) complex that identifies a function of LRRK2 in regulating membrane fusion at the trans-Golgi network (TGN). At the TGN, LRRK2 further interacts with the Golgi SNAREs VAMP4 and Syntaxin-6 and acts as a scaffolding platform that stabilizes the GARP-SNAREs complex formation. Therefore, LRRK2 influences both retrograde and post-Golgi trafficking pathways in a manner dependent on its GTP binding and kinase activity. This action is exaggerated by mutations associated with Parkinson’s disease and can be blocked by kinase inhibitors. Disruption of GARP sensitizes dopamine neurons to mutant LRRK2 toxicity in C. elegans, showing that these pathways are interlinked in vivo and suggesting a link in PD.
Document Type: article in journal/newspaper
File Description: text
Language: English
Relation: https://discovery.ucl.ac.uk/id/eprint/10096349/
Availability: https://discovery.ucl.ac.uk/id/eprint/10096349/8/1-s2.0-S2211124720305635-main%20%281%29.pdf; https://discovery.ucl.ac.uk/id/eprint/10096349/
Rights: open
Accession Number: edsbas.695049FF
Database: BASE