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Codon-Specific Translation by m(1)G37 Methylation of tRNA

Although the genetic code is degenerate, synonymous codons for the same amino acid are not translated equally. Codon-specific translation is important for controlling gene expression and determining the proteome of a cell. At the molecular level, codon-specific translation is regulated by post-trans...

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Autores principales: Hou, Ya-Ming, Masuda, Isao, Gamper, Howard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6335274/
https://www.ncbi.nlm.nih.gov/pubmed/30687389
http://dx.doi.org/10.3389/fgene.2018.00713
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author Hou, Ya-Ming
Masuda, Isao
Gamper, Howard
author_facet Hou, Ya-Ming
Masuda, Isao
Gamper, Howard
author_sort Hou, Ya-Ming
collection PubMed
description Although the genetic code is degenerate, synonymous codons for the same amino acid are not translated equally. Codon-specific translation is important for controlling gene expression and determining the proteome of a cell. At the molecular level, codon-specific translation is regulated by post-transcriptional epigenetic modifications of tRNA primarily at the wobble position 34 and at position 37 on the 3′-side of the anticodon. Modifications at these positions determine the quality of codon-anticodon pairing and the speed of translation on the ribosome. Different modifications operate in distinct mechanisms of codon-specific translation, generating a diversity of regulation that is previously unanticipated. Here we summarize recent work that demonstrates codon-specific translation mediated by the m(1)G37 methylation of tRNA at CCC and CCU codons for proline, an amino acid that has unique features in translation.
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spelling pubmed-63352742019-01-25 Codon-Specific Translation by m(1)G37 Methylation of tRNA Hou, Ya-Ming Masuda, Isao Gamper, Howard Front Genet Genetics Although the genetic code is degenerate, synonymous codons for the same amino acid are not translated equally. Codon-specific translation is important for controlling gene expression and determining the proteome of a cell. At the molecular level, codon-specific translation is regulated by post-transcriptional epigenetic modifications of tRNA primarily at the wobble position 34 and at position 37 on the 3′-side of the anticodon. Modifications at these positions determine the quality of codon-anticodon pairing and the speed of translation on the ribosome. Different modifications operate in distinct mechanisms of codon-specific translation, generating a diversity of regulation that is previously unanticipated. Here we summarize recent work that demonstrates codon-specific translation mediated by the m(1)G37 methylation of tRNA at CCC and CCU codons for proline, an amino acid that has unique features in translation. Frontiers Media S.A. 2019-01-10 /pmc/articles/PMC6335274/ /pubmed/30687389 http://dx.doi.org/10.3389/fgene.2018.00713 Text en Copyright © 2019 Hou, Masuda and Gamper. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Hou, Ya-Ming
Masuda, Isao
Gamper, Howard
Codon-Specific Translation by m(1)G37 Methylation of tRNA
title Codon-Specific Translation by m(1)G37 Methylation of tRNA
title_full Codon-Specific Translation by m(1)G37 Methylation of tRNA
title_fullStr Codon-Specific Translation by m(1)G37 Methylation of tRNA
title_full_unstemmed Codon-Specific Translation by m(1)G37 Methylation of tRNA
title_short Codon-Specific Translation by m(1)G37 Methylation of tRNA
title_sort codon-specific translation by m(1)g37 methylation of trna
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6335274/
https://www.ncbi.nlm.nih.gov/pubmed/30687389
http://dx.doi.org/10.3389/fgene.2018.00713
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