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Coordination among tertiary base pairs results in an efficient frameshift-stimulating RNA pseudoknot
Frameshifting is an essential process that regulates protein synthesis in many viruses. The ribosome may slip backward when encountering a frameshift motif on the messenger RNA, which usually contains a pseudoknot structure involving tertiary base pair interactions. Due to the lack of detailed molec...
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/PMC5449628/ https://www.ncbi.nlm.nih.gov/pubmed/28334864 http://dx.doi.org/10.1093/nar/gkx134 |
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author | Chen, Yu-Ting Chang, Kai-Chun Hu, Hao-Teng Chen, Yi-Lan Lin, You-Hsin Hsu, Chiung-Fang Chang, Cheng-Fu Chang, Kung-Yao Wen, Jin-Der |
author_facet | Chen, Yu-Ting Chang, Kai-Chun Hu, Hao-Teng Chen, Yi-Lan Lin, You-Hsin Hsu, Chiung-Fang Chang, Cheng-Fu Chang, Kung-Yao Wen, Jin-Der |
author_sort | Chen, Yu-Ting |
collection | PubMed |
description | Frameshifting is an essential process that regulates protein synthesis in many viruses. The ribosome may slip backward when encountering a frameshift motif on the messenger RNA, which usually contains a pseudoknot structure involving tertiary base pair interactions. Due to the lack of detailed molecular explanations, previous studies investigating which features of the pseudoknot are important to stimulate frameshifting have presented diverse conclusions. Here we constructed a bimolecular pseudoknot to dissect the interior tertiary base pairs and used single-molecule approaches to assess the structure targeted by ribosomes. We found that the first ribosome target stem was resistant to unwinding when the neighboring loop was confined along the stem; such constrained conformation was dependent on the presence of consecutive adenosines in this loop. Mutations that disrupted the distal base triples abolished all remaining tertiary base pairs. Changes in frameshifting efficiency correlated with the stem unwinding resistance. Our results demonstrate that various tertiary base pairs are coordinated inside a highly efficient frameshift-stimulating RNA pseudoknot and suggest a mechanism by which mechanical resistance of the pseudoknot may persistently act on translocating ribosomes. |
format | Online Article Text |
id | pubmed-5449628 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-54496282017-06-05 Coordination among tertiary base pairs results in an efficient frameshift-stimulating RNA pseudoknot Chen, Yu-Ting Chang, Kai-Chun Hu, Hao-Teng Chen, Yi-Lan Lin, You-Hsin Hsu, Chiung-Fang Chang, Cheng-Fu Chang, Kung-Yao Wen, Jin-Der Nucleic Acids Res RNA Frameshifting is an essential process that regulates protein synthesis in many viruses. The ribosome may slip backward when encountering a frameshift motif on the messenger RNA, which usually contains a pseudoknot structure involving tertiary base pair interactions. Due to the lack of detailed molecular explanations, previous studies investigating which features of the pseudoknot are important to stimulate frameshifting have presented diverse conclusions. Here we constructed a bimolecular pseudoknot to dissect the interior tertiary base pairs and used single-molecule approaches to assess the structure targeted by ribosomes. We found that the first ribosome target stem was resistant to unwinding when the neighboring loop was confined along the stem; such constrained conformation was dependent on the presence of consecutive adenosines in this loop. Mutations that disrupted the distal base triples abolished all remaining tertiary base pairs. Changes in frameshifting efficiency correlated with the stem unwinding resistance. Our results demonstrate that various tertiary base pairs are coordinated inside a highly efficient frameshift-stimulating RNA pseudoknot and suggest a mechanism by which mechanical resistance of the pseudoknot may persistently act on translocating ribosomes. Oxford University Press 2017-06-02 2017-02-21 /pmc/articles/PMC5449628/ /pubmed/28334864 http://dx.doi.org/10.1093/nar/gkx134 Text en © The Author(s) 2017. 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 Chen, Yu-Ting Chang, Kai-Chun Hu, Hao-Teng Chen, Yi-Lan Lin, You-Hsin Hsu, Chiung-Fang Chang, Cheng-Fu Chang, Kung-Yao Wen, Jin-Der Coordination among tertiary base pairs results in an efficient frameshift-stimulating RNA pseudoknot |
title | Coordination among tertiary base pairs results in an efficient frameshift-stimulating RNA pseudoknot |
title_full | Coordination among tertiary base pairs results in an efficient frameshift-stimulating RNA pseudoknot |
title_fullStr | Coordination among tertiary base pairs results in an efficient frameshift-stimulating RNA pseudoknot |
title_full_unstemmed | Coordination among tertiary base pairs results in an efficient frameshift-stimulating RNA pseudoknot |
title_short | Coordination among tertiary base pairs results in an efficient frameshift-stimulating RNA pseudoknot |
title_sort | coordination among tertiary base pairs results in an efficient frameshift-stimulating rna pseudoknot |
topic | RNA |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5449628/ https://www.ncbi.nlm.nih.gov/pubmed/28334864 http://dx.doi.org/10.1093/nar/gkx134 |
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