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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
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. |
format | Online Article Text |
id | pubmed-5389517 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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