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Transfer RNAs with novel cloverleaf structures

We report the identification of novel tRNA species with 12-base pair amino-acid acceptor branches composed of longer acceptor stem and shorter T-stem. While canonical tRNAs have a 7/5 configuration of the branch, the novel tRNAs have either 8/4 or 9/3 structure. They were found during the search for...

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Autores principales: Mukai, Takahito, Vargas-Rodriguez, Oscar, Englert, Markus, Tripp, H. James, Ivanova, Natalia N., Rubin, Edward M., Kyrpides, Nikos C., Söll, Dieter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
RNA
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5389517/
https://www.ncbi.nlm.nih.gov/pubmed/28076288
http://dx.doi.org/10.1093/nar/gkw898
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author Mukai, Takahito
Vargas-Rodriguez, Oscar
Englert, Markus
Tripp, H. James
Ivanova, Natalia N.
Rubin, Edward M.
Kyrpides, Nikos C.
Söll, Dieter
author_facet Mukai, Takahito
Vargas-Rodriguez, Oscar
Englert, Markus
Tripp, H. James
Ivanova, Natalia N.
Rubin, Edward M.
Kyrpides, Nikos C.
Söll, Dieter
author_sort Mukai, Takahito
collection PubMed
description We report the identification of novel tRNA species with 12-base pair amino-acid acceptor branches composed of longer acceptor stem and shorter T-stem. While canonical tRNAs have a 7/5 configuration of the branch, the novel tRNAs have either 8/4 or 9/3 structure. They were found during the search for selenocysteine tRNAs in terabytes of genome, metagenome and metatranscriptome sequences. Certain bacteria and their phages employ the 8/4 structure for serine and histidine tRNAs, while minor cysteine and selenocysteine tRNA species may have a modified 8/4 structure with one bulge nucleotide. In Acidobacteria, tRNAs with 8/4 and 9/3 structures may function as missense and nonsense suppressor tRNAs and/or regulatory noncoding RNAs. In δ-proteobacteria, an additional cysteine tRNA with an 8/4 structure mimics selenocysteine tRNA and may function as opal suppressor. We examined the potential translation function of suppressor tRNA species in Escherichia coli; tRNAs with 8/4 or 9/3 structures efficiently inserted serine, alanine and cysteine in response to stop and sense codons, depending on the identity element and anticodon sequence of the tRNA. These findings expand our view of how tRNA, and possibly the genetic code, is diversified in nature.
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spelling pubmed-53895172017-04-24 Transfer RNAs with novel cloverleaf structures Mukai, Takahito Vargas-Rodriguez, Oscar Englert, Markus Tripp, H. James Ivanova, Natalia N. Rubin, Edward M. Kyrpides, Nikos C. Söll, Dieter Nucleic Acids Res RNA We report the identification of novel tRNA species with 12-base pair amino-acid acceptor branches composed of longer acceptor stem and shorter T-stem. While canonical tRNAs have a 7/5 configuration of the branch, the novel tRNAs have either 8/4 or 9/3 structure. They were found during the search for selenocysteine tRNAs in terabytes of genome, metagenome and metatranscriptome sequences. Certain bacteria and their phages employ the 8/4 structure for serine and histidine tRNAs, while minor cysteine and selenocysteine tRNA species may have a modified 8/4 structure with one bulge nucleotide. In Acidobacteria, tRNAs with 8/4 and 9/3 structures may function as missense and nonsense suppressor tRNAs and/or regulatory noncoding RNAs. In δ-proteobacteria, an additional cysteine tRNA with an 8/4 structure mimics selenocysteine tRNA and may function as opal suppressor. We examined the potential translation function of suppressor tRNA species in Escherichia coli; tRNAs with 8/4 or 9/3 structures efficiently inserted serine, alanine and cysteine in response to stop and sense codons, depending on the identity element and anticodon sequence of the tRNA. These findings expand our view of how tRNA, and possibly the genetic code, is diversified in nature. Oxford University Press 2017-03-17 2016-10-05 /pmc/articles/PMC5389517/ /pubmed/28076288 http://dx.doi.org/10.1093/nar/gkw898 Text en © The Author(s) 2016. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle RNA
Mukai, Takahito
Vargas-Rodriguez, Oscar
Englert, Markus
Tripp, H. James
Ivanova, Natalia N.
Rubin, Edward M.
Kyrpides, Nikos C.
Söll, Dieter
Transfer RNAs with novel cloverleaf structures
title Transfer RNAs with novel cloverleaf structures
title_full Transfer RNAs with novel cloverleaf structures
title_fullStr Transfer RNAs with novel cloverleaf structures
title_full_unstemmed Transfer RNAs with novel cloverleaf structures
title_short Transfer RNAs with novel cloverleaf structures
title_sort transfer rnas with novel cloverleaf structures
topic RNA
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5389517/
https://www.ncbi.nlm.nih.gov/pubmed/28076288
http://dx.doi.org/10.1093/nar/gkw898
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