RNA-Induced Conformational Switching and Clustering of G3BP Drive Stress Granule Assembly by Condensation.

ABSTRACT: Stressed cells shut down translation, release mRNA molecules from polysomes, and form stress granules (SGs) via a network of interactions that involve G3BP. Here we focus on the mechanistic underpinnings of SG assembly. We show that, under non-stress conditions, G3BP adopts a compact auto-inhibited state stabilized by electrostatic intramolecular interactions between the intrinsically disordered acidic tracts and the positively charged arginine-rich region. Upon release from polysomes, unfolded mRNAs outcompete G3BP auto-inhibitory interactions, engendering a conformational transition that facilitates clustering of G3BP through protein-RNA interactions. Subsequent physical crosslinking of G3BP clusters drives RNA molecules into networked RNA/protein condensates. We show that G3BP condensat

SUBMITTER: Guillen-Boixet J 

PROVIDER: S-EPMC7181197 | biostudies-literature | 2020 Apr

REPOSITORIES: biostudies-literature