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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Taylor & Francis
2020
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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. |
format | Online Article Text |
id | pubmed-7237155 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
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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