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Viral RNA structure-based strategies to manipulate translation

Viruses must co-opt the cellular translation machinery to produce progeny virions. Eukaryotic viruses have evolved a variety of ways to manipulate the cellular translation apparatus, in many cases using elegant RNA-centred strategies. Viral RNAs can alter or control every phase of protein synthesis...

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Detalles Bibliográficos
Autores principales: Jaafar, Zane A., Kieft, Jeffrey S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6452865/
https://www.ncbi.nlm.nih.gov/pubmed/30514982
http://dx.doi.org/10.1038/s41579-018-0117-x
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author Jaafar, Zane A.
Kieft, Jeffrey S.
author_facet Jaafar, Zane A.
Kieft, Jeffrey S.
author_sort Jaafar, Zane A.
collection PubMed
description Viruses must co-opt the cellular translation machinery to produce progeny virions. Eukaryotic viruses have evolved a variety of ways to manipulate the cellular translation apparatus, in many cases using elegant RNA-centred strategies. Viral RNAs can alter or control every phase of protein synthesis and have diverse targets, mechanisms and structures. In addition, as cells attempt to limit infection by downregulating translation, some of these viral RNAs enable the virus to overcome this response or even take advantage of it to promote viral translation over cellular translation. In this Review, we present important examples of viral RNA-based strategies to exploit the cellular translation machinery. We describe what is understood of the structures and mechanisms of diverse viral RNA elements that alter or regulate translation, the advantages that are conferred to the virus and some of the major unknowns that provide motivation for further exploration.
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spelling pubmed-64528652019-04-08 Viral RNA structure-based strategies to manipulate translation Jaafar, Zane A. Kieft, Jeffrey S. Nat Rev Microbiol Review Article Viruses must co-opt the cellular translation machinery to produce progeny virions. Eukaryotic viruses have evolved a variety of ways to manipulate the cellular translation apparatus, in many cases using elegant RNA-centred strategies. Viral RNAs can alter or control every phase of protein synthesis and have diverse targets, mechanisms and structures. In addition, as cells attempt to limit infection by downregulating translation, some of these viral RNAs enable the virus to overcome this response or even take advantage of it to promote viral translation over cellular translation. In this Review, we present important examples of viral RNA-based strategies to exploit the cellular translation machinery. We describe what is understood of the structures and mechanisms of diverse viral RNA elements that alter or regulate translation, the advantages that are conferred to the virus and some of the major unknowns that provide motivation for further exploration. Nature Publishing Group UK 2018-12-04 2019 /pmc/articles/PMC6452865/ /pubmed/30514982 http://dx.doi.org/10.1038/s41579-018-0117-x Text en © Springer Nature Limited 2018 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Review Article
Jaafar, Zane A.
Kieft, Jeffrey S.
Viral RNA structure-based strategies to manipulate translation
title Viral RNA structure-based strategies to manipulate translation
title_full Viral RNA structure-based strategies to manipulate translation
title_fullStr Viral RNA structure-based strategies to manipulate translation
title_full_unstemmed Viral RNA structure-based strategies to manipulate translation
title_short Viral RNA structure-based strategies to manipulate translation
title_sort viral rna structure-based strategies to manipulate translation
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6452865/
https://www.ncbi.nlm.nih.gov/pubmed/30514982
http://dx.doi.org/10.1038/s41579-018-0117-x
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