Paper

M6A reduction relieves FUS-associated ALS granules

Grandioso, Alessia, Castagnetti, Francesco, Di Timoteo, Gaia, Perego, Eleonora, Bozzoni, Irene, Lisi, Michela, Sabatelli, Mario, Giuliani, Andrea, Rotili, Dante, Setti, Adriano, Mariani, Davide, Zappone, Sabrina, Vicidomini, Giuseppe, Lattante, Serena, Biagi, Martina C.

2023

Overview

Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease due to gradual motorneurons (MN) degeneration1. Among the processes associated to ALS pathogenesis, there is the formation of cytoplasmic inclusions produced by mutant protein aggregation, among which the RNA binding protein FUS2. In this work we show that such inclusions are significantly reduced in number and dissolve faster when the RNA m6A content is diminished as a consequence of the m6A writer METTL3 knock-down. These effects were observed both in neuronal cell lines and in iPSC-derived human motor neurons expressing mutant FUS. Importantly, stress granules formed in ALS condition showed a distinctive transcriptome with respect to control cells; interestingly, after METTL3 downregulation, it reverted to similar to control. Finally, we show that FUS inclusions are reduced also in patient-derived fibroblasts treated with STM-2457, a well characterized inhibitor of METTL3 activity, paving the way for its possible use for counteracting aggregate formation in ALS.

• Publisher: Cold Spring Harbor Laboratory
• Subject: Molecular Biology