Cargando…
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...
Autores principales: | , , , , , , , , , , , |
---|---|
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 |
_version_ | 1783664646791626752 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7957426 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT navarroisabelacunha translationaladaptationtoheatstressismediatedbyrna5methylcytosineincaenorhabditiselegans AT tuortofrancesca translationaladaptationtoheatstressismediatedbyrna5methylcytosineincaenorhabditiselegans AT jordandavid translationaladaptationtoheatstressismediatedbyrna5methylcytosineincaenorhabditiselegans AT legrandcarine translationaladaptationtoheatstressismediatedbyrna5methylcytosineincaenorhabditiselegans AT pricejonathan translationaladaptationtoheatstressismediatedbyrna5methylcytosineincaenorhabditiselegans AT braukmannfabian translationaladaptationtoheatstressismediatedbyrna5methylcytosineincaenorhabditiselegans AT hendrickalang translationaladaptationtoheatstressismediatedbyrna5methylcytosineincaenorhabditiselegans AT akayalper translationaladaptationtoheatstressismediatedbyrna5methylcytosineincaenorhabditiselegans AT kotterannika translationaladaptationtoheatstressismediatedbyrna5methylcytosineincaenorhabditiselegans AT helmmark translationaladaptationtoheatstressismediatedbyrna5methylcytosineincaenorhabditiselegans AT lykofrank translationaladaptationtoheatstressismediatedbyrna5methylcytosineincaenorhabditiselegans AT miskaerica translationaladaptationtoheatstressismediatedbyrna5methylcytosineincaenorhabditiselegans |