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Journal Article

N4-acetylcytidine (ac4C) promotes mRNA localization to stress granules

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Meierhofer,  David       
Mass Spectrometry Facility (Head: David Meierhofer), Scientific Service (Head: Claudia Thurow), Max Planck Institute for Molecular Genetics, Max Planck Society;

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EMBO Reports_Kudrin et al_2024.pdf
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Citation

Kudrin, P., Singh, A., Meierhofer, D., Kuśnierczyk, A., & Ørom, U. A. V. (2024). N4-acetylcytidine (ac4C) promotes mRNA localization to stress granules. EMBO Reports, 25(4), 1814-1834. doi:10.1038/s44319-024-00098-6.


Cite as: https://hdl.handle.net/21.11116/0000-000E-82CE-7
Abstract
Stress granules are an integral part of the stress response that are formed from non-translating mRNAs aggregated with proteins. While much is known about stress granules, the factors that drive their mRNA localization are incompletely described. Modification of mRNA can alter the properties of the nucleobases and affect processes such as translation, splicing and localization of individual transcripts. Here, we show that the RNA modification N4-acetylcytidine (ac4C) on mRNA associates with transcripts enriched in stress granules and that stress granule localized transcripts with ac4C are specifically translationally regulated. We also show that ac4C on mRNA can mediate localization of the protein NOP58 to stress granules. Our results suggest that acetylation of mRNA regulates localization of both stress-sensitive transcripts and RNA-binding proteins to stress granules and adds to our understanding of the molecular mechanisms responsible for stress granule formation.