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Yeast Ataxin-2 Forms an Intracellular Condensate Required for the Inhibition of TORC1 Signaling during Respiratory Growth
Author(s) -
Yu-San Yang,
Masato Kato,
Xi Wu,
Athanasios Litsios,
Benjamin M. Sutter,
Yun Wang,
Chien-Hsiang Hsu,
N. Ezgi Wood,
Andrew Lemoff,
Hamid Mirzaei,
Matthias Heinemann,
Benjamin P. Tu
Publication year - 2019
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2019.02.043
Subject(s) - biology , microbiology and biotechnology , stress granule , autophagy , yeast , intracellular , mutant , regulator , mitochondrion , signal transduction , biochemistry , translation (biology) , gene , apoptosis , messenger rna
Yeast ataxin-2, also known as Pbp1 (polyA binding protein-binding protein 1), is an intrinsically disordered protein implicated in stress granule formation, RNA biology, and neurodegenerative disease. To understand the endogenous function of this protein, we identify Pbp1 as a dedicated regulator of TORC1 signaling and autophagy under conditions that require mitochondrial respiration. Pbp1 binds to TORC1 specifically during respiratory growth, but utilizes an additional methionine-rich, low complexity (LC) region to inhibit TORC1. This LC region causes phase separation, forms reversible fibrils, and enables self-association into assemblies required for TORC1 inhibition. Mutants that weaken phase separation in vitro exhibit reduced capacity to inhibit TORC1 and induce autophagy. Loss of Pbp1 leads to mitochondrial dysfunction and reduced fitness during nutritional stress. Thus, Pbp1 forms a condensate in response to respiratory status to regulate TORC1 signaling.

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