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Complete chemical structures of human mitochondrial tRNAs

Mitochondria generate most cellular energy via oxidative phosphorylation. Twenty-two species of mitochondrial (mt-)tRNAs encoded in mtDNA translate essential subunits of the respiratory chain complexes. mt-tRNAs contain post-transcriptional modifications introduced by nuclear-encoded tRNA-modifying...

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Autores principales: Suzuki, Takeo, Yashiro, Yuka, Kikuchi, Ittoku, Ishigami, Yuma, Saito, Hironori, Matsuzawa, Ikuya, Okada, Shunpei, Mito, Mari, Iwasaki, Shintaro, Ma, Ding, Zhao, Xuewei, Asano, Kana, Lin, Huan, Kirino, Yohei, Sakaguchi, Yuriko, Suzuki, Tsutomu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7455718/
https://www.ncbi.nlm.nih.gov/pubmed/32859890
http://dx.doi.org/10.1038/s41467-020-18068-6
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author Suzuki, Takeo
Yashiro, Yuka
Kikuchi, Ittoku
Ishigami, Yuma
Saito, Hironori
Matsuzawa, Ikuya
Okada, Shunpei
Mito, Mari
Iwasaki, Shintaro
Ma, Ding
Zhao, Xuewei
Asano, Kana
Lin, Huan
Kirino, Yohei
Sakaguchi, Yuriko
Suzuki, Tsutomu
author_facet Suzuki, Takeo
Yashiro, Yuka
Kikuchi, Ittoku
Ishigami, Yuma
Saito, Hironori
Matsuzawa, Ikuya
Okada, Shunpei
Mito, Mari
Iwasaki, Shintaro
Ma, Ding
Zhao, Xuewei
Asano, Kana
Lin, Huan
Kirino, Yohei
Sakaguchi, Yuriko
Suzuki, Tsutomu
author_sort Suzuki, Takeo
collection PubMed
description Mitochondria generate most cellular energy via oxidative phosphorylation. Twenty-two species of mitochondrial (mt-)tRNAs encoded in mtDNA translate essential subunits of the respiratory chain complexes. mt-tRNAs contain post-transcriptional modifications introduced by nuclear-encoded tRNA-modifying enzymes. They are required for deciphering genetic code accurately, as well as stabilizing tRNA. Loss of tRNA modifications frequently results in severe pathological consequences. Here, we perform a comprehensive analysis of post-transcriptional modifications of all human mt-tRNAs, including 14 previously-uncharacterized species. In total, we find 18 kinds of RNA modifications at 137 positions (8.7% in 1575 nucleobases) in 22 species of human mt-tRNAs. An up-to-date list of 34 genes responsible for mt-tRNA modifications are provided. We identify two genes required for queuosine (Q) formation in mt-tRNAs. Our results provide insight into the molecular mechanisms underlying the decoding system and could help to elucidate the molecular pathogenesis of human mitochondrial diseases caused by aberrant tRNA modifications.
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spelling pubmed-74557182020-09-04 Complete chemical structures of human mitochondrial tRNAs Suzuki, Takeo Yashiro, Yuka Kikuchi, Ittoku Ishigami, Yuma Saito, Hironori Matsuzawa, Ikuya Okada, Shunpei Mito, Mari Iwasaki, Shintaro Ma, Ding Zhao, Xuewei Asano, Kana Lin, Huan Kirino, Yohei Sakaguchi, Yuriko Suzuki, Tsutomu Nat Commun Article Mitochondria generate most cellular energy via oxidative phosphorylation. Twenty-two species of mitochondrial (mt-)tRNAs encoded in mtDNA translate essential subunits of the respiratory chain complexes. mt-tRNAs contain post-transcriptional modifications introduced by nuclear-encoded tRNA-modifying enzymes. They are required for deciphering genetic code accurately, as well as stabilizing tRNA. Loss of tRNA modifications frequently results in severe pathological consequences. Here, we perform a comprehensive analysis of post-transcriptional modifications of all human mt-tRNAs, including 14 previously-uncharacterized species. In total, we find 18 kinds of RNA modifications at 137 positions (8.7% in 1575 nucleobases) in 22 species of human mt-tRNAs. An up-to-date list of 34 genes responsible for mt-tRNA modifications are provided. We identify two genes required for queuosine (Q) formation in mt-tRNAs. Our results provide insight into the molecular mechanisms underlying the decoding system and could help to elucidate the molecular pathogenesis of human mitochondrial diseases caused by aberrant tRNA modifications. Nature Publishing Group UK 2020-08-28 /pmc/articles/PMC7455718/ /pubmed/32859890 http://dx.doi.org/10.1038/s41467-020-18068-6 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Suzuki, Takeo
Yashiro, Yuka
Kikuchi, Ittoku
Ishigami, Yuma
Saito, Hironori
Matsuzawa, Ikuya
Okada, Shunpei
Mito, Mari
Iwasaki, Shintaro
Ma, Ding
Zhao, Xuewei
Asano, Kana
Lin, Huan
Kirino, Yohei
Sakaguchi, Yuriko
Suzuki, Tsutomu
Complete chemical structures of human mitochondrial tRNAs
title Complete chemical structures of human mitochondrial tRNAs
title_full Complete chemical structures of human mitochondrial tRNAs
title_fullStr Complete chemical structures of human mitochondrial tRNAs
title_full_unstemmed Complete chemical structures of human mitochondrial tRNAs
title_short Complete chemical structures of human mitochondrial tRNAs
title_sort complete chemical structures of human mitochondrial trnas
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7455718/
https://www.ncbi.nlm.nih.gov/pubmed/32859890
http://dx.doi.org/10.1038/s41467-020-18068-6
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