The protective role of m1A during stress-induced granulation

Author:

Alriquet Marion12,Calloni Giulia12,Martínez-Limón Adrían12,Delli Ponti Riccardo345,Hanspach Gerd6,Hengesbach Martin6ORCID,Tartaglia Gian G.34578,Vabulas R. Martin12

Affiliation:

1. Buchmann Institute for Molecular Life Sciences, Goethe University Frankfurt, 60438 Frankfurt am Main, Germany

2. Institute of Biophysical Chemistry, Goethe University Frankfurt, 60438 Frankfurt am Main, Germany

3. Centre for Genomic Regulation (CRG), The Barcelona Institute for Science and Technology, 08003 Barcelona, Spain

4. Universitat Pompeu Fabra (UPF), 08003 Barcelona, Spain

5. Institucio Catalana de Recerca i Estudis Avançats (ICREA), 08010 Barcelona, Spain

6. Institute for Organic Chemistry and Chemical Biology, Goethe University Frankfurt, 60438 Frankfurt am Main, Germany

7. Department of Biology ‘Charles Darwin’, Sapienza University of Rome, 00185 Rome, Italy

8. Department of Neuroscience and Brain Technologies, Istituto Italiano di Tecnologia, 16163 Genoa, Italy

Abstract

Abstract Post-transcriptional methylation of N6-adenine and N1-adenine can affect transcriptome turnover and translation. Furthermore, the regulatory function of N6-methyladenine (m6A) 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 (m1A) on mRNAs during acute stress response remains largely unknown. Here we show that the methyltransferase complex TRMT6/61A, which generates the m1A tag, is involved in transcriptome protection during heat shock. Our bioinformatics analysis indicates that occurrence of the m1A motif is increased in mRNAs known to be enriched in SGs. Accordingly, the m1A-generating methyltransferase TRMT6/61A accumulated in SGs and mass spectrometry confirmed enrichment of m1A 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.

Funder

European Research Council

H2020

Spanish Ministry of Economy and Competitiveness

Deutsche Forschungsgemeinschaft

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Genetics,Molecular Biology,General Medicine

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