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Regulation of stress granules in virus systems

Virus infection initiates a number of cellular stress responses that modulate gene regulation and compartmentalization of RNA. Viruses must control host gene expression and the localization of viral RNAs to be successful parasites. RNA granules such as stress granules and processing bodies (PBs) con...

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Detalles Bibliográficos
Autores principales: White, James P., Lloyd, Richard E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3322245/
https://www.ncbi.nlm.nih.gov/pubmed/22405519
http://dx.doi.org/10.1016/j.tim.2012.02.001
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author White, James P.
Lloyd, Richard E.
author_facet White, James P.
Lloyd, Richard E.
author_sort White, James P.
collection PubMed
description Virus infection initiates a number of cellular stress responses that modulate gene regulation and compartmentalization of RNA. Viruses must control host gene expression and the localization of viral RNAs to be successful parasites. RNA granules such as stress granules and processing bodies (PBs) contain translationally silenced messenger ribonucleoproteins (mRNPs) and serve as extensions of translation regulation in cells, storing transiently repressed mRNAs. New reports show a growing number of virus families modulate RNA granule function to maximize replication efficiency. This review summarizes recent advances in understanding the relationship between viruses and mRNA stress granules in animal cells and will discuss important questions that remain in this emerging field.
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spelling pubmed-33222452013-04-01 Regulation of stress granules in virus systems White, James P. Lloyd, Richard E. Trends Microbiol Review Virus infection initiates a number of cellular stress responses that modulate gene regulation and compartmentalization of RNA. Viruses must control host gene expression and the localization of viral RNAs to be successful parasites. RNA granules such as stress granules and processing bodies (PBs) contain translationally silenced messenger ribonucleoproteins (mRNPs) and serve as extensions of translation regulation in cells, storing transiently repressed mRNAs. New reports show a growing number of virus families modulate RNA granule function to maximize replication efficiency. This review summarizes recent advances in understanding the relationship between viruses and mRNA stress granules in animal cells and will discuss important questions that remain in this emerging field. Elsevier Ltd. 2012-04 2012-03-07 /pmc/articles/PMC3322245/ /pubmed/22405519 http://dx.doi.org/10.1016/j.tim.2012.02.001 Text en Copyright © 2012 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 Review
White, James P.
Lloyd, Richard E.
Regulation of stress granules in virus systems
title Regulation of stress granules in virus systems
title_full Regulation of stress granules in virus systems
title_fullStr Regulation of stress granules in virus systems
title_full_unstemmed Regulation of stress granules in virus systems
title_short Regulation of stress granules in virus systems
title_sort regulation of stress granules in virus systems
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3322245/
https://www.ncbi.nlm.nih.gov/pubmed/22405519
http://dx.doi.org/10.1016/j.tim.2012.02.001
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