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Translational adaptation to heat stress is mediated by RNA 5‐methylcytosine in Caenorhabditis elegans

Methylation of carbon‐5 of cytosines (m(5)C) is a post‐transcriptional nucleotide modification of RNA found in all kingdoms of life. While individual m(5)C‐methyltransferases have been studied, the impact of the global cytosine‐5 methylome on development, homeostasis and stress remains unknown. Here...

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Autores principales: Navarro, Isabela Cunha, Tuorto, Francesca, Jordan, David, Legrand, Carine, Price, Jonathan, Braukmann, Fabian, Hendrick, Alan G, Akay, Alper, Kotter, Annika, Helm, Mark, Lyko, Frank, Miska, Eric A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7957426/
https://www.ncbi.nlm.nih.gov/pubmed/33283887
http://dx.doi.org/10.15252/embj.2020105496
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author Navarro, Isabela Cunha
Tuorto, Francesca
Jordan, David
Legrand, Carine
Price, Jonathan
Braukmann, Fabian
Hendrick, Alan G
Akay, Alper
Kotter, Annika
Helm, Mark
Lyko, Frank
Miska, Eric A
author_facet Navarro, Isabela Cunha
Tuorto, Francesca
Jordan, David
Legrand, Carine
Price, Jonathan
Braukmann, Fabian
Hendrick, Alan G
Akay, Alper
Kotter, Annika
Helm, Mark
Lyko, Frank
Miska, Eric A
author_sort Navarro, Isabela Cunha
collection PubMed
description Methylation of carbon‐5 of cytosines (m(5)C) is a post‐transcriptional nucleotide modification of RNA found in all kingdoms of life. While individual m(5)C‐methyltransferases have been studied, the impact of the global cytosine‐5 methylome on development, homeostasis and stress remains unknown. Here, using Caenorhabditis elegans, we generated the first organism devoid of m(5)C in RNA, demonstrating that this modification is non‐essential. Using this genetic tool, we determine the localisation and enzymatic specificity of m(5)C sites in the RNome in vivo. We find that NSUN‐4 acts as a dual rRNA and tRNA methyltransferase in C. elegans mitochondria. In agreement with leucine and proline being the most frequently methylated tRNA isoacceptors, loss of m(5)C impacts the decoding of some triplets of these two amino acids, leading to reduced translation efficiency. Upon heat stress, m(5)C loss leads to ribosome stalling at UUG triplets, the only codon translated by an m(5)C34‐modified tRNA. This leads to reduced translation efficiency of UUG‐rich transcripts and impaired fertility, suggesting a role of m(5)C tRNA wobble methylation in the adaptation to higher temperatures.
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spelling pubmed-79574262021-03-19 Translational adaptation to heat stress is mediated by RNA 5‐methylcytosine in Caenorhabditis elegans Navarro, Isabela Cunha Tuorto, Francesca Jordan, David Legrand, Carine Price, Jonathan Braukmann, Fabian Hendrick, Alan G Akay, Alper Kotter, Annika Helm, Mark Lyko, Frank Miska, Eric A EMBO J Articles Methylation of carbon‐5 of cytosines (m(5)C) is a post‐transcriptional nucleotide modification of RNA found in all kingdoms of life. While individual m(5)C‐methyltransferases have been studied, the impact of the global cytosine‐5 methylome on development, homeostasis and stress remains unknown. Here, using Caenorhabditis elegans, we generated the first organism devoid of m(5)C in RNA, demonstrating that this modification is non‐essential. Using this genetic tool, we determine the localisation and enzymatic specificity of m(5)C sites in the RNome in vivo. We find that NSUN‐4 acts as a dual rRNA and tRNA methyltransferase in C. elegans mitochondria. In agreement with leucine and proline being the most frequently methylated tRNA isoacceptors, loss of m(5)C impacts the decoding of some triplets of these two amino acids, leading to reduced translation efficiency. Upon heat stress, m(5)C loss leads to ribosome stalling at UUG triplets, the only codon translated by an m(5)C34‐modified tRNA. This leads to reduced translation efficiency of UUG‐rich transcripts and impaired fertility, suggesting a role of m(5)C tRNA wobble methylation in the adaptation to higher temperatures. John Wiley and Sons Inc. 2020-12-07 2021-03-15 /pmc/articles/PMC7957426/ /pubmed/33283887 http://dx.doi.org/10.15252/embj.2020105496 Text en © 2020 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Navarro, Isabela Cunha
Tuorto, Francesca
Jordan, David
Legrand, Carine
Price, Jonathan
Braukmann, Fabian
Hendrick, Alan G
Akay, Alper
Kotter, Annika
Helm, Mark
Lyko, Frank
Miska, Eric A
Translational adaptation to heat stress is mediated by RNA 5‐methylcytosine in Caenorhabditis elegans
title Translational adaptation to heat stress is mediated by RNA 5‐methylcytosine in Caenorhabditis elegans
title_full Translational adaptation to heat stress is mediated by RNA 5‐methylcytosine in Caenorhabditis elegans
title_fullStr Translational adaptation to heat stress is mediated by RNA 5‐methylcytosine in Caenorhabditis elegans
title_full_unstemmed Translational adaptation to heat stress is mediated by RNA 5‐methylcytosine in Caenorhabditis elegans
title_short Translational adaptation to heat stress is mediated by RNA 5‐methylcytosine in Caenorhabditis elegans
title_sort translational adaptation to heat stress is mediated by rna 5‐methylcytosine in caenorhabditis elegans
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7957426/
https://www.ncbi.nlm.nih.gov/pubmed/33283887
http://dx.doi.org/10.15252/embj.2020105496
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