Journal Article

A complex of C9ORF72 and p62 uses arginine methylation to eliminate stress granules by autophagy

Zinman, Lorne, Palidwor, Gareth, Rogaeva, Ekaterina, Bondy-Chorney, Emma, Couture, Jean-François, Barry, Francesca A., Woulfe, John, Savard, Alexandre, Lavallée-Adam, Mathieu, Jagow, Chantal, Tremblay, Veronique, Côté, Jocelyn, Gibbings, Derrick, Keith, Julia, Paris, Geneviève, Chitiprolu, Maneka, Robertson, Janice

2018

Overview

Mutations in proteins like FUS which cause Amyotrophic Lateral Sclerosis (ALS) result in the aberrant formation of stress granules while ALS-linked mutations in other proteins impede elimination of stress granules. Repeat expansions in C9ORF72, the major cause of ALS, reduce C9ORF72 levels but how this impacts stress granules is uncertain. Here, we demonstrate that C9ORF72 associates with the autophagy receptor p62 and controls elimination of stress granules by autophagy. This requires p62 to associate via the Tudor protein SMN with proteins, including FUS, that are symmetrically methylated on arginines. Mice lacking p62 accumulate arginine-methylated proteins and alterations in FUS-dependent splicing. Patients with C9ORF72 repeat expansions accumulate symmetric arginine dimethylated proteins which co-localize with p62. This suggests that C9ORF72 initiates a cascade of ALS-linked proteins (C9ORF72, p62, SMN, FUS) to recognize stress granules for degradation by autophagy and hallmarks of a defect in this process are observable in ALS patients. Many Amyotrophic Lateral Sclerosis (ALS)-linked mutations cause accumulation of stress granules, and most ALS cases are caused by repeat expansions in C9ORF72. Here the authors show that C9ORF72 and the autophagy receptor p62 interact to associate with proteins symmetrically dimethylated on arginines such as FUS, to eliminate stress granules by autophagy.

• Publisher: Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
• Subject: 13/51 / 13/89 / 14/19 / 14/28 / 631/337/458/1648 / 631/80/39/2346 / 64/60 / 692/699/375/1917/1285 / 82/58 / 82/81 / 82/83 / Amyotrophic lateral sclerosis / Amyotrophic Lateral Sclerosis - genetics / Amyotrophic Lateral Sclerosis - metabolism / Amyotrophic Lateral Sclerosis - pathology / Animals / Arginine / Arginine - metabolism / Autophagy / Autophagy - genetics / C9orf72 Protein - genetics / C9orf72 Protein - metabolism / Cell Line, Tumor / Cytoplasmic Granules - metabolism / Cytoplasmic Granules - pathology / Embryo, Mammalian / Granular materials / HeLa Cells / Humanities and Social Sciences / Humans / Methylation / Mice / Mice, Knockout / Motor Neurons - cytology / Motor Neurons - metabolism / multidisciplinary / Mutation / Patients / Phagocytosis / Primary Cell Culture / Protein-Arginine N-Methyltransferases - genetics / Protein-Arginine N-Methyltransferases - metabolism / Proteins / RNA-Binding Protein FUS - genetics / RNA-Binding Protein FUS - metabolism / Science / Science (multidisciplinary) / Sequestosome-1 Protein - genetics / Sequestosome-1 Protein - metabolism / Splicing / Stress, Physiological / Stresses / Survival of Motor Neuron 1 Protein - genetics / Survival of Motor Neuron 1 Protein - metabolism