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Journal article

M6A reduction relieves FUS-associated ALS granules

Abstract:
Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease due to gradual motoneurons (MN) degeneration. Among the processes associated to ALS pathogenesis, there is the formation of cytoplasmic inclusions produced by aggregation of mutant proteins, among which the RNA binding protein FUS. Here we show that, in neuronal cells and in iPSC-derived MN expressing mutant FUS, such inclusions are significantly reduced in number and dissolve faster when the RNA m6A content is diminished. Interestingly, stress granules formed in ALS conditions showed a distinctive transcriptome with respect to control cells, which reverted to similar to control after m6A downregulation. Notably, cells expressing mutant FUS were characterized by higher m6A levels suggesting a possible link between m6A homeostasis and pathological aggregates. Finally, we show that FUS inclusions are reduced also in patient-derived fibroblasts treated with STM-2457, an inhibitor of METTL3 activity, paving the way for its possible use for counteracting aggregate formation in ALS
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1038/s41467-024-49416-5

Authors

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Role:
Author
ORCID:
0000-0003-4516-9945
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Institution:
University of Oxford
Role:
Author
ORCID:
0009-0002-2327-3792
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Role:
Author
ORCID:
0000-0002-4995-2403
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Role:
Author
ORCID:
0009-0002-4597-9796
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Role:
Author
ORCID:
0000-0003-0360-4777


Publisher:
Nature Research
Journal:
Nature Communications More from this journal
Volume:
15
Issue:
1
Pages:
5033-5033
Publication date:
2024-06-12
DOI:
EISSN:
2041-1723
ISSN:
2041-1723


Language:
English
Keywords:
Pubs id:
2371054
Local pid:
pubs:2371054
Source identifiers:
W4399562598
Deposit date:
2026-02-13
ARK identifier:
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