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Genome recoding by tRNA modifications

RNA modifications are emerging as an additional regulatory layer on top of the primary RNA sequence. These modifications are particularly enriched in tRNAs where they can regulate not only global protein translation, but also protein translation at the codon level. Modifications located in or in the...

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Detalles Bibliográficos
Autores principales: Tuorto, Francesca, Lyko, Frank
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5204126/
https://www.ncbi.nlm.nih.gov/pubmed/27974624
http://dx.doi.org/10.1098/rsob.160287
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author Tuorto, Francesca
Lyko, Frank
author_facet Tuorto, Francesca
Lyko, Frank
author_sort Tuorto, Francesca
collection PubMed
description RNA modifications are emerging as an additional regulatory layer on top of the primary RNA sequence. These modifications are particularly enriched in tRNAs where they can regulate not only global protein translation, but also protein translation at the codon level. Modifications located in or in the vicinity of tRNA anticodons are highly conserved in eukaryotes and have been identified as potential regulators of mRNA decoding. Recent studies have provided novel insights into how these modifications orchestrate the speed and fidelity of translation to ensure proper protein homeostasis. This review highlights the prominent modifications in the tRNA anticodon loop: queuosine, inosine, 5-methoxycarbonylmethyl-2-thiouridine, wybutosine, threonyl–carbamoyl–adenosine and 5-methylcytosine. We discuss the functional relevance of these modifications in protein translation and their emerging role in eukaryotic genome recoding during cellular adaptation and disease.
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spelling pubmed-52041262017-01-05 Genome recoding by tRNA modifications Tuorto, Francesca Lyko, Frank Open Biol Review RNA modifications are emerging as an additional regulatory layer on top of the primary RNA sequence. These modifications are particularly enriched in tRNAs where they can regulate not only global protein translation, but also protein translation at the codon level. Modifications located in or in the vicinity of tRNA anticodons are highly conserved in eukaryotes and have been identified as potential regulators of mRNA decoding. Recent studies have provided novel insights into how these modifications orchestrate the speed and fidelity of translation to ensure proper protein homeostasis. This review highlights the prominent modifications in the tRNA anticodon loop: queuosine, inosine, 5-methoxycarbonylmethyl-2-thiouridine, wybutosine, threonyl–carbamoyl–adenosine and 5-methylcytosine. We discuss the functional relevance of these modifications in protein translation and their emerging role in eukaryotic genome recoding during cellular adaptation and disease. The Royal Society 2016-12-14 /pmc/articles/PMC5204126/ /pubmed/27974624 http://dx.doi.org/10.1098/rsob.160287 Text en © 2016 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Review
Tuorto, Francesca
Lyko, Frank
Genome recoding by tRNA modifications
title Genome recoding by tRNA modifications
title_full Genome recoding by tRNA modifications
title_fullStr Genome recoding by tRNA modifications
title_full_unstemmed Genome recoding by tRNA modifications
title_short Genome recoding by tRNA modifications
title_sort genome recoding by trna modifications
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5204126/
https://www.ncbi.nlm.nih.gov/pubmed/27974624
http://dx.doi.org/10.1098/rsob.160287
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