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Structural signatures of thermal adaptation of bacterial ribosomal RNA, transfer RNA, and messenger RNA
Temperature adaptation of bacterial RNAs is a subject of both fundamental and practical interest because it will allow a better understanding of molecular mechanism of RNA folding with potential industrial application of functional thermophilic or psychrophilic RNAs. Here, we performed a comprehensi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5598986/ https://www.ncbi.nlm.nih.gov/pubmed/28910383 http://dx.doi.org/10.1371/journal.pone.0184722 |
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author | Jegousse, Clara Yang, Yuedong Zhan, Jian Wang, Jihua Zhou, Yaoqi |
author_facet | Jegousse, Clara Yang, Yuedong Zhan, Jian Wang, Jihua Zhou, Yaoqi |
author_sort | Jegousse, Clara |
collection | PubMed |
description | Temperature adaptation of bacterial RNAs is a subject of both fundamental and practical interest because it will allow a better understanding of molecular mechanism of RNA folding with potential industrial application of functional thermophilic or psychrophilic RNAs. Here, we performed a comprehensive study of rRNA, tRNA, and mRNA of more than 200 bacterial species with optimal growth temperatures (OGT) ranging from 4°C to 95°C. We investigated temperature adaptation at primary, secondary and tertiary structure levels. We showed that unlike mRNA, tRNA and rRNA were optimized for their structures at compositional levels with significant tertiary structural features even for their corresponding randomly permutated sequences. tRNA and rRNA are more exposed to solvent but remain structured for hyperthermophiles with nearly OGT-independent fluctuation of solvent accessible surface area within a single RNA chain. mRNA in hyperthermophiles is essentially the same as random sequences without tertiary structures although many mRNA in mesophiles and psychrophiles have well-defined tertiary structures based on their low overall solvent exposure with clear separation of deeply buried from partly exposed bases as in tRNA and rRNA. These results provide new insight into temperature adaptation of different RNAs. |
format | Online Article Text |
id | pubmed-5598986 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-55989862017-09-22 Structural signatures of thermal adaptation of bacterial ribosomal RNA, transfer RNA, and messenger RNA Jegousse, Clara Yang, Yuedong Zhan, Jian Wang, Jihua Zhou, Yaoqi PLoS One Research Article Temperature adaptation of bacterial RNAs is a subject of both fundamental and practical interest because it will allow a better understanding of molecular mechanism of RNA folding with potential industrial application of functional thermophilic or psychrophilic RNAs. Here, we performed a comprehensive study of rRNA, tRNA, and mRNA of more than 200 bacterial species with optimal growth temperatures (OGT) ranging from 4°C to 95°C. We investigated temperature adaptation at primary, secondary and tertiary structure levels. We showed that unlike mRNA, tRNA and rRNA were optimized for their structures at compositional levels with significant tertiary structural features even for their corresponding randomly permutated sequences. tRNA and rRNA are more exposed to solvent but remain structured for hyperthermophiles with nearly OGT-independent fluctuation of solvent accessible surface area within a single RNA chain. mRNA in hyperthermophiles is essentially the same as random sequences without tertiary structures although many mRNA in mesophiles and psychrophiles have well-defined tertiary structures based on their low overall solvent exposure with clear separation of deeply buried from partly exposed bases as in tRNA and rRNA. These results provide new insight into temperature adaptation of different RNAs. Public Library of Science 2017-09-14 /pmc/articles/PMC5598986/ /pubmed/28910383 http://dx.doi.org/10.1371/journal.pone.0184722 Text en © 2017 Jegousse et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Jegousse, Clara Yang, Yuedong Zhan, Jian Wang, Jihua Zhou, Yaoqi Structural signatures of thermal adaptation of bacterial ribosomal RNA, transfer RNA, and messenger RNA |
title | Structural signatures of thermal adaptation of bacterial ribosomal RNA, transfer RNA, and messenger RNA |
title_full | Structural signatures of thermal adaptation of bacterial ribosomal RNA, transfer RNA, and messenger RNA |
title_fullStr | Structural signatures of thermal adaptation of bacterial ribosomal RNA, transfer RNA, and messenger RNA |
title_full_unstemmed | Structural signatures of thermal adaptation of bacterial ribosomal RNA, transfer RNA, and messenger RNA |
title_short | Structural signatures of thermal adaptation of bacterial ribosomal RNA, transfer RNA, and messenger RNA |
title_sort | structural signatures of thermal adaptation of bacterial ribosomal rna, transfer rna, and messenger rna |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5598986/ https://www.ncbi.nlm.nih.gov/pubmed/28910383 http://dx.doi.org/10.1371/journal.pone.0184722 |
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