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TRMT2B is responsible for both tRNA and rRNA m(5)U-methylation in human mitochondria

RNA species play host to a plethora of post-transcriptional modifications which together make up the epitranscriptome. 5-methyluridine (m(5)U) is one of the most common modifications made to cellular RNA, where it is found almost ubiquitously in bacterial and eukaryotic cytosolic tRNAs at position 5...

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Autores principales: Powell, Christopher A., Minczuk, Michal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7237155/
https://www.ncbi.nlm.nih.gov/pubmed/31948311
http://dx.doi.org/10.1080/15476286.2020.1712544
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author Powell, Christopher A.
Minczuk, Michal
author_facet Powell, Christopher A.
Minczuk, Michal
author_sort Powell, Christopher A.
collection PubMed
description RNA species play host to a plethora of post-transcriptional modifications which together make up the epitranscriptome. 5-methyluridine (m(5)U) is one of the most common modifications made to cellular RNA, where it is found almost ubiquitously in bacterial and eukaryotic cytosolic tRNAs at position 54. Here, we demonstrate that m(5)U54 in human mitochondrial tRNAs is catalysed by the nuclear-encoded enzyme TRMT2B, and that its repertoire of substrates is expanded to ribosomal RNAs, catalysing m(5)U429 in 12S rRNA. We show that TRMT2B is not essential for viability in human cells and that knocking-out the gene shows no obvious phenotype with regards to RNA stability, mitochondrial translation, or cellular growth.
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spelling pubmed-72371552020-05-29 TRMT2B is responsible for both tRNA and rRNA m(5)U-methylation in human mitochondria Powell, Christopher A. Minczuk, Michal RNA Biol Research Paper RNA species play host to a plethora of post-transcriptional modifications which together make up the epitranscriptome. 5-methyluridine (m(5)U) is one of the most common modifications made to cellular RNA, where it is found almost ubiquitously in bacterial and eukaryotic cytosolic tRNAs at position 54. Here, we demonstrate that m(5)U54 in human mitochondrial tRNAs is catalysed by the nuclear-encoded enzyme TRMT2B, and that its repertoire of substrates is expanded to ribosomal RNAs, catalysing m(5)U429 in 12S rRNA. We show that TRMT2B is not essential for viability in human cells and that knocking-out the gene shows no obvious phenotype with regards to RNA stability, mitochondrial translation, or cellular growth. Taylor & Francis 2020-01-17 /pmc/articles/PMC7237155/ /pubmed/31948311 http://dx.doi.org/10.1080/15476286.2020.1712544 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Paper
Powell, Christopher A.
Minczuk, Michal
TRMT2B is responsible for both tRNA and rRNA m(5)U-methylation in human mitochondria
title TRMT2B is responsible for both tRNA and rRNA m(5)U-methylation in human mitochondria
title_full TRMT2B is responsible for both tRNA and rRNA m(5)U-methylation in human mitochondria
title_fullStr TRMT2B is responsible for both tRNA and rRNA m(5)U-methylation in human mitochondria
title_full_unstemmed TRMT2B is responsible for both tRNA and rRNA m(5)U-methylation in human mitochondria
title_short TRMT2B is responsible for both tRNA and rRNA m(5)U-methylation in human mitochondria
title_sort trmt2b is responsible for both trna and rrna m(5)u-methylation in human mitochondria
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7237155/
https://www.ncbi.nlm.nih.gov/pubmed/31948311
http://dx.doi.org/10.1080/15476286.2020.1712544
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