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Strategies for viral RNA stability: live long and prosper

Eukaryotic cells have a powerful RNA decay machinery that plays an important and diverse role in regulating both the quantity and the quality of gene expression. Viral RNAs need to successfully navigate around this cellular machinery to initiate and maintain a highly productive infection. Recent wor...

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Detalles Bibliográficos
Autores principales: Dickson, Alexa M., Wilusz, Jeffrey
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3123725/
https://www.ncbi.nlm.nih.gov/pubmed/21640425
http://dx.doi.org/10.1016/j.tig.2011.04.003
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author Dickson, Alexa M.
Wilusz, Jeffrey
author_facet Dickson, Alexa M.
Wilusz, Jeffrey
author_sort Dickson, Alexa M.
collection PubMed
description Eukaryotic cells have a powerful RNA decay machinery that plays an important and diverse role in regulating both the quantity and the quality of gene expression. Viral RNAs need to successfully navigate around this cellular machinery to initiate and maintain a highly productive infection. Recent work has shown that viruses have developed a variety of strategies to accomplish this, including inherent RNA shields, hijacking host RNA stability factors, incapacitating the host decay machinery and changing the entire landscape of RNA stability in cells using virally encoded nucleases. In addition to maintaining the stability of viral transcripts, these strategies can also contribute to the regulation and complexity of viral gene expression as well as to viral RNA evolution.
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spelling pubmed-31237252012-07-01 Strategies for viral RNA stability: live long and prosper Dickson, Alexa M. Wilusz, Jeffrey Trends Genet Article Eukaryotic cells have a powerful RNA decay machinery that plays an important and diverse role in regulating both the quantity and the quality of gene expression. Viral RNAs need to successfully navigate around this cellular machinery to initiate and maintain a highly productive infection. Recent work has shown that viruses have developed a variety of strategies to accomplish this, including inherent RNA shields, hijacking host RNA stability factors, incapacitating the host decay machinery and changing the entire landscape of RNA stability in cells using virally encoded nucleases. In addition to maintaining the stability of viral transcripts, these strategies can also contribute to the regulation and complexity of viral gene expression as well as to viral RNA evolution. Elsevier Ltd. 2011-07 2011-06-03 /pmc/articles/PMC3123725/ /pubmed/21640425 http://dx.doi.org/10.1016/j.tig.2011.04.003 Text en Copyright © 2011 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Dickson, Alexa M.
Wilusz, Jeffrey
Strategies for viral RNA stability: live long and prosper
title Strategies for viral RNA stability: live long and prosper
title_full Strategies for viral RNA stability: live long and prosper
title_fullStr Strategies for viral RNA stability: live long and prosper
title_full_unstemmed Strategies for viral RNA stability: live long and prosper
title_short Strategies for viral RNA stability: live long and prosper
title_sort strategies for viral rna stability: live long and prosper
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3123725/
https://www.ncbi.nlm.nih.gov/pubmed/21640425
http://dx.doi.org/10.1016/j.tig.2011.04.003
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