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The protective role of m(1)A during stress-induced granulation

Post-transcriptional methylation of N6-adenine and N1-adenine can affect transcriptome turnover and translation. Furthermore, the regulatory function of N6-methyladenine (m(6)A) during heat shock has been uncovered, including the enhancement of the phase separation potential of RNAs. In response to...

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Autores principales: Alriquet, Marion, Calloni, Giulia, Martínez-Limón, Adrían, Delli Ponti, Riccardo, Hanspach, Gerd, Hengesbach, Martin, Tartaglia, Gian G., Vabulas, R. Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7883823/
https://www.ncbi.nlm.nih.gov/pubmed/32462207
http://dx.doi.org/10.1093/jmcb/mjaa023
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author Alriquet, Marion
Calloni, Giulia
Martínez-Limón, Adrían
Delli Ponti, Riccardo
Hanspach, Gerd
Hengesbach, Martin
Tartaglia, Gian G.
Vabulas, R. Martin
author_facet Alriquet, Marion
Calloni, Giulia
Martínez-Limón, Adrían
Delli Ponti, Riccardo
Hanspach, Gerd
Hengesbach, Martin
Tartaglia, Gian G.
Vabulas, R. Martin
author_sort Alriquet, Marion
collection PubMed
description Post-transcriptional methylation of N6-adenine and N1-adenine can affect transcriptome turnover and translation. Furthermore, the regulatory function of N6-methyladenine (m(6)A) during heat shock has been uncovered, including the enhancement of the phase separation potential of RNAs. In response to acute stress, e.g. heat shock, the orderly sequestration of mRNAs in stress granules (SGs) is considered important to protect transcripts from the irreversible aggregation. Until recently, the role of N1-methyladenine (m(1)A) on mRNAs during acute stress response remains largely unknown. Here we show that the methyltransferase complex TRMT6/61A, which generates the m(1)A tag, is involved in transcriptome protection during heat shock. Our bioinformatics analysis indicates that occurrence of the m(1)A motif is increased in mRNAs known to be enriched in SGs. Accordingly, the m(1)A-generating methyltransferase TRMT6/61A accumulated in SGs and mass spectrometry confirmed enrichment of m(1)A in the SG RNAs. The insertion of a single methylation motif in the untranslated region of a reporter RNA leads to more efficient recovery of protein synthesis from that transcript after the return to normal temperature. Our results demonstrate far-reaching functional consequences of a minimal RNA modification on N1-adenine during acute proteostasis stress.
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spelling pubmed-78838232021-02-18 The protective role of m(1)A during stress-induced granulation Alriquet, Marion Calloni, Giulia Martínez-Limón, Adrían Delli Ponti, Riccardo Hanspach, Gerd Hengesbach, Martin Tartaglia, Gian G. Vabulas, R. Martin J Mol Cell Biol Articles Post-transcriptional methylation of N6-adenine and N1-adenine can affect transcriptome turnover and translation. Furthermore, the regulatory function of N6-methyladenine (m(6)A) during heat shock has been uncovered, including the enhancement of the phase separation potential of RNAs. In response to acute stress, e.g. heat shock, the orderly sequestration of mRNAs in stress granules (SGs) is considered important to protect transcripts from the irreversible aggregation. Until recently, the role of N1-methyladenine (m(1)A) on mRNAs during acute stress response remains largely unknown. Here we show that the methyltransferase complex TRMT6/61A, which generates the m(1)A tag, is involved in transcriptome protection during heat shock. Our bioinformatics analysis indicates that occurrence of the m(1)A motif is increased in mRNAs known to be enriched in SGs. Accordingly, the m(1)A-generating methyltransferase TRMT6/61A accumulated in SGs and mass spectrometry confirmed enrichment of m(1)A in the SG RNAs. The insertion of a single methylation motif in the untranslated region of a reporter RNA leads to more efficient recovery of protein synthesis from that transcript after the return to normal temperature. Our results demonstrate far-reaching functional consequences of a minimal RNA modification on N1-adenine during acute proteostasis stress. Oxford University Press 2020-05-27 /pmc/articles/PMC7883823/ /pubmed/32462207 http://dx.doi.org/10.1093/jmcb/mjaa023 Text en © The Author(s) (2020). Published by Oxford University Press on behalf of Journal of Molecular Cell Biology, IBCB, SIBS, CAS. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Articles
Alriquet, Marion
Calloni, Giulia
Martínez-Limón, Adrían
Delli Ponti, Riccardo
Hanspach, Gerd
Hengesbach, Martin
Tartaglia, Gian G.
Vabulas, R. Martin
The protective role of m(1)A during stress-induced granulation
title The protective role of m(1)A during stress-induced granulation
title_full The protective role of m(1)A during stress-induced granulation
title_fullStr The protective role of m(1)A during stress-induced granulation
title_full_unstemmed The protective role of m(1)A during stress-induced granulation
title_short The protective role of m(1)A during stress-induced granulation
title_sort protective role of m(1)a during stress-induced granulation
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7883823/
https://www.ncbi.nlm.nih.gov/pubmed/32462207
http://dx.doi.org/10.1093/jmcb/mjaa023
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