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Mechanism and structural diversity of exoribonuclease-resistant RNA structures in flaviviral RNAs
Flaviviruses such as Yellow fever, Dengue, West Nile, and Zika generate disease-linked viral noncoding RNAs called subgenomic flavivirus RNAs. Subgenomic flavivirus RNAs result when the 5′–3′ progression of cellular exoribonuclease Xrn1 is blocked by RNA elements called Xrn1-resistant RNAs located w...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5760640/ https://www.ncbi.nlm.nih.gov/pubmed/29317714 http://dx.doi.org/10.1038/s41467-017-02604-y |
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author | MacFadden, Andrea O’Donoghue, Zoe Silva, Patricia A. G. C. Chapman, Erich G. Olsthoorn, René C. Sterken, Mark G. Pijlman, Gorben P. Bredenbeek, Peter J. Kieft, Jeffrey S. |
author_facet | MacFadden, Andrea O’Donoghue, Zoe Silva, Patricia A. G. C. Chapman, Erich G. Olsthoorn, René C. Sterken, Mark G. Pijlman, Gorben P. Bredenbeek, Peter J. Kieft, Jeffrey S. |
author_sort | MacFadden, Andrea |
collection | PubMed |
description | Flaviviruses such as Yellow fever, Dengue, West Nile, and Zika generate disease-linked viral noncoding RNAs called subgenomic flavivirus RNAs. Subgenomic flavivirus RNAs result when the 5′–3′ progression of cellular exoribonuclease Xrn1 is blocked by RNA elements called Xrn1-resistant RNAs located within the viral genome’s 3′-untranslated region that operate without protein co-factors. Here, we show that Xrn1-resistant RNAs can halt diverse exoribonucleases, revealing a mechanism in which they act as general mechanical blocks that ‘brace’ against an enzyme’s surface, presenting an unfolding problem that confounds further enzyme progression. Further, we directly demonstrate that Xrn1-resistant RNAs exist in a diverse set of flaviviruses, including some specific to insects or with no known arthropod vector. These Xrn1-resistant RNAs comprise two secondary structural classes that mirror previously reported phylogenic analysis. Our discoveries have implications for the evolution of exoribonuclease resistance, the use of Xrn1-resistant RNAs in synthetic biology, and the development of new therapies. |
format | Online Article Text |
id | pubmed-5760640 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57606402018-01-12 Mechanism and structural diversity of exoribonuclease-resistant RNA structures in flaviviral RNAs MacFadden, Andrea O’Donoghue, Zoe Silva, Patricia A. G. C. Chapman, Erich G. Olsthoorn, René C. Sterken, Mark G. Pijlman, Gorben P. Bredenbeek, Peter J. Kieft, Jeffrey S. Nat Commun Article Flaviviruses such as Yellow fever, Dengue, West Nile, and Zika generate disease-linked viral noncoding RNAs called subgenomic flavivirus RNAs. Subgenomic flavivirus RNAs result when the 5′–3′ progression of cellular exoribonuclease Xrn1 is blocked by RNA elements called Xrn1-resistant RNAs located within the viral genome’s 3′-untranslated region that operate without protein co-factors. Here, we show that Xrn1-resistant RNAs can halt diverse exoribonucleases, revealing a mechanism in which they act as general mechanical blocks that ‘brace’ against an enzyme’s surface, presenting an unfolding problem that confounds further enzyme progression. Further, we directly demonstrate that Xrn1-resistant RNAs exist in a diverse set of flaviviruses, including some specific to insects or with no known arthropod vector. These Xrn1-resistant RNAs comprise two secondary structural classes that mirror previously reported phylogenic analysis. Our discoveries have implications for the evolution of exoribonuclease resistance, the use of Xrn1-resistant RNAs in synthetic biology, and the development of new therapies. Nature Publishing Group UK 2018-01-09 /pmc/articles/PMC5760640/ /pubmed/29317714 http://dx.doi.org/10.1038/s41467-017-02604-y Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article MacFadden, Andrea O’Donoghue, Zoe Silva, Patricia A. G. C. Chapman, Erich G. Olsthoorn, René C. Sterken, Mark G. Pijlman, Gorben P. Bredenbeek, Peter J. Kieft, Jeffrey S. Mechanism and structural diversity of exoribonuclease-resistant RNA structures in flaviviral RNAs |
title | Mechanism and structural diversity of exoribonuclease-resistant RNA structures in flaviviral RNAs |
title_full | Mechanism and structural diversity of exoribonuclease-resistant RNA structures in flaviviral RNAs |
title_fullStr | Mechanism and structural diversity of exoribonuclease-resistant RNA structures in flaviviral RNAs |
title_full_unstemmed | Mechanism and structural diversity of exoribonuclease-resistant RNA structures in flaviviral RNAs |
title_short | Mechanism and structural diversity of exoribonuclease-resistant RNA structures in flaviviral RNAs |
title_sort | mechanism and structural diversity of exoribonuclease-resistant rna structures in flaviviral rnas |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5760640/ https://www.ncbi.nlm.nih.gov/pubmed/29317714 http://dx.doi.org/10.1038/s41467-017-02604-y |
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