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Cytosine-5 RNA methylation links protein synthesis to cell metabolism.

Accepted version
Peer-reviewed

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Authors

Gkatza, Nikoletta A  ORCID logo  https://orcid.org/0000-0001-6360-7940
Castro, Cecilia 
Harvey, Robert F 
Popis, Martyna C 

Abstract

Posttranscriptional modifications in transfer RNA (tRNA) are often critical for normal development because they adapt protein synthesis rates to a dynamically changing microenvironment. However, the precise cellular mechanisms linking the extrinsic stimulus to the intrinsic RNA modification pathways remain largely unclear. Here, we identified the cytosine-5 RNA methyltransferase NSUN2 as a sensor for external stress stimuli. Exposure to oxidative stress efficiently repressed NSUN2, causing a reduction of methylation at specific tRNA sites. Using metabolic profiling, we showed that loss of tRNA methylation captured cells in a distinct catabolic state. Mechanistically, loss of NSUN2 altered the biogenesis of tRNA-derived noncoding fragments (tRFs) in response to stress, leading to impaired regulation of protein synthesis. The intracellular accumulation of a specific subset of tRFs correlated with the dynamic repression of global protein synthesis. Finally, NSUN2-driven RNA methylation was functionally required to adapt cell cycle progression to the early stress response. In summary, we revealed that changes in tRNA methylation profiles were sufficient to specify cellular metabolic states and efficiently adapt protein synthesis rates to cell stress.

Description

Keywords

Animals, Cell Line, Cytosine, DNA Methylation, DNA-Cytosine Methylases, Humans, Methyltransferases, Mice, Oxidative Stress, Protein Biosynthesis, RNA, RNA, Transfer

Journal Title

PLoS Biol

Conference Name

Journal ISSN

1544-9173
1545-7885

Volume Title

17

Publisher

Public Library of Science (PLoS)

Rights

All rights reserved
Sponsorship
Cancer Research Uk (None)
European Research Council (310360)
Medical Research Council (MR/M01939X/1)
Wellcome Trust (097922/Z/11/Z)
Medical Research Council (MR/P011705/1)
Cancer Research Uk (None)
Medical Research Council (MC_PC_12009)
Medical Research Council (MR/P01836X/1)
Medical Research Council (MC_PC_13030)
This work was funded by a Cancer Research UK Senior Fellowship (C10701/A15181), the European Research Council (ERC; 310360), and the Medical Research Council UK (MR/M01939X/1). Part of this work was carried out in the framework of the European COST action EPITRAN 16120. SK receives funding from the DFG (KE1943/3-1). The funders had no role in study design, data collection, and analysis, decision to publish, 5 or preparation of the manuscript.