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All genera of Flaviviridae host a conserved Xrn1-resistant RNA motif
After infection by flaviviruses like Zika and West Nile virus, eukaryotic hosts employ the well-conserved endoribonuclease Xrn1 to degrade the viral genomic RNA. Within the 3ʹ untranslated regions, this enzyme encounters intricate Xrn1-resistant structures. This results in the accumulation of subgen...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8632102/ https://www.ncbi.nlm.nih.gov/pubmed/33858294 http://dx.doi.org/10.1080/15476286.2021.1907044 |
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author | Dilweg, Ivar W. Savina, Anya Köthe, Susanne Gultyaev, Alexander P. Bredenbeek, Peter J. Olsthoorn, René C.L. |
author_facet | Dilweg, Ivar W. Savina, Anya Köthe, Susanne Gultyaev, Alexander P. Bredenbeek, Peter J. Olsthoorn, René C.L. |
author_sort | Dilweg, Ivar W. |
collection | PubMed |
description | After infection by flaviviruses like Zika and West Nile virus, eukaryotic hosts employ the well-conserved endoribonuclease Xrn1 to degrade the viral genomic RNA. Within the 3ʹ untranslated regions, this enzyme encounters intricate Xrn1-resistant structures. This results in the accumulation of subgenomic flaviviral RNAs, an event that improves viral growth and aggravates viral pathogenicity. Xrn1-resistant RNAs have been established throughout the flaviviral genus, but not yet throughout the entire Flaviviridae family. In this work, we use previously determined characteristics of these structures to identify homologous sequences in many members of the genera pegivirus, hepacivirus and pestivirus. We used structural alignment and mutational analyses to establish that these sequences indeed represent Xrn1-resistant RNA and that they employ the general features of the flaviviral xrRNAs, consisting of a double pseudoknot formed by five base-paired regions stitched together by a crucial triple base interaction. Furthermore, we demonstrate that the pestivirus Bungowannah virus produces subgenomic RNA in vivo. Altogether, these results indicate that viruses make use of a universal Xrn1-resistant RNA throughout the Flaviviridae family. |
format | Online Article Text |
id | pubmed-8632102 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-86321022021-12-01 All genera of Flaviviridae host a conserved Xrn1-resistant RNA motif Dilweg, Ivar W. Savina, Anya Köthe, Susanne Gultyaev, Alexander P. Bredenbeek, Peter J. Olsthoorn, René C.L. RNA Biol Research Paper After infection by flaviviruses like Zika and West Nile virus, eukaryotic hosts employ the well-conserved endoribonuclease Xrn1 to degrade the viral genomic RNA. Within the 3ʹ untranslated regions, this enzyme encounters intricate Xrn1-resistant structures. This results in the accumulation of subgenomic flaviviral RNAs, an event that improves viral growth and aggravates viral pathogenicity. Xrn1-resistant RNAs have been established throughout the flaviviral genus, but not yet throughout the entire Flaviviridae family. In this work, we use previously determined characteristics of these structures to identify homologous sequences in many members of the genera pegivirus, hepacivirus and pestivirus. We used structural alignment and mutational analyses to establish that these sequences indeed represent Xrn1-resistant RNA and that they employ the general features of the flaviviral xrRNAs, consisting of a double pseudoknot formed by five base-paired regions stitched together by a crucial triple base interaction. Furthermore, we demonstrate that the pestivirus Bungowannah virus produces subgenomic RNA in vivo. Altogether, these results indicate that viruses make use of a universal Xrn1-resistant RNA throughout the Flaviviridae family. Taylor & Francis 2021-04-16 /pmc/articles/PMC8632102/ /pubmed/33858294 http://dx.doi.org/10.1080/15476286.2021.1907044 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way. |
spellingShingle | Research Paper Dilweg, Ivar W. Savina, Anya Köthe, Susanne Gultyaev, Alexander P. Bredenbeek, Peter J. Olsthoorn, René C.L. All genera of Flaviviridae host a conserved Xrn1-resistant RNA motif |
title | All genera of Flaviviridae host a conserved Xrn1-resistant RNA motif |
title_full | All genera of Flaviviridae host a conserved Xrn1-resistant RNA motif |
title_fullStr | All genera of Flaviviridae host a conserved Xrn1-resistant RNA motif |
title_full_unstemmed | All genera of Flaviviridae host a conserved Xrn1-resistant RNA motif |
title_short | All genera of Flaviviridae host a conserved Xrn1-resistant RNA motif |
title_sort | all genera of flaviviridae host a conserved xrn1-resistant rna motif |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8632102/ https://www.ncbi.nlm.nih.gov/pubmed/33858294 http://dx.doi.org/10.1080/15476286.2021.1907044 |
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