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As a matter of fat: Emerging roles of lipid-sensitive E3 ubiquitin ligases.

Accepted version
Peer-reviewed

Type

Article

Change log

Authors

Gawden-Bone, Christian M  ORCID logo  https://orcid.org/0000-0003-0413-3727
Lehner, Paul J 
Volkmar, Norbert 

Abstract

The dynamic structure and composition of lipid membranes need to be tightly regulated to control the vast array of cellular processes from cell and organelle morphology to protein-protein interactions and signal transduction pathways. To maintain membrane integrity, sense-and-response systems monitor and adjust membrane lipid composition to the ever-changing cellular environment, but only a relatively small number of control systems have been described. Here, we explore the emerging role of the ubiquitin-proteasome system in monitoring and maintaining membrane lipid composition. We focus on the ER-resident RNF145 E3 ubiquitin ligase, its role in regulating adiponectin receptor 2 (ADIPOR2), its lipid hydrolase substrate, and the broader implications for understanding the homeostatic processes that fine-tune cellular membrane composition.

Description

Keywords

ADIPOR2, E3 ubiquitin ligases, RNF145, homeoviscous adaption, lipids, protein degradation, Ubiquitin-Protein Ligases, Ubiquitination, Ubiquitin, Proteasome Endopeptidase Complex, Membrane Lipids

Journal Title

Bioessays

Conference Name

Journal ISSN

0265-9247
1521-1878

Volume Title

Publisher

Wiley
Sponsorship
Wellcome Trust (210688/Z/18/Z)