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Actin’ up: Herpesvirus Interactions with Rho GTPase Signaling

Herpesviruses constitute a very large and diverse family of DNA viruses, which can generally be subdivided in alpha-, beta- and gammaherpesvirus subfamilies. Increasing evidence indicates that many herpesviruses interact with cytoskeleton-regulating Rho GTPase signaling pathways during different pha...

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Detalles Bibliográficos
Autores principales: Van den Broeke, Céline, Favoreel, Herman W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185701/
https://www.ncbi.nlm.nih.gov/pubmed/21994732
http://dx.doi.org/10.3390/v3040278
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author Van den Broeke, Céline
Favoreel, Herman W.
author_facet Van den Broeke, Céline
Favoreel, Herman W.
author_sort Van den Broeke, Céline
collection PubMed
description Herpesviruses constitute a very large and diverse family of DNA viruses, which can generally be subdivided in alpha-, beta- and gammaherpesvirus subfamilies. Increasing evidence indicates that many herpesviruses interact with cytoskeleton-regulating Rho GTPase signaling pathways during different phases of their replication cycle. Because of the large differences between herpesvirus subfamilies, the molecular mechanisms and specific consequences of individual herpesvirus interactions with Rho GTPase signaling may differ. However, some evolutionary distinct but similar general effects on Rho GTPase signaling and the cytoskeleton have also been reported. Examples of these include Rho GTPase-mediated nuclear translocation of virus during entry in a host cell and Rho GTPase-mediated viral cell-to-cell spread during later stages of infection. The current review gives an overview of both general and individual interactions of herpesviruses with Rho GTPase signaling.
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spelling pubmed-31857012011-10-12 Actin’ up: Herpesvirus Interactions with Rho GTPase Signaling Van den Broeke, Céline Favoreel, Herman W. Viruses Review Herpesviruses constitute a very large and diverse family of DNA viruses, which can generally be subdivided in alpha-, beta- and gammaherpesvirus subfamilies. Increasing evidence indicates that many herpesviruses interact with cytoskeleton-regulating Rho GTPase signaling pathways during different phases of their replication cycle. Because of the large differences between herpesvirus subfamilies, the molecular mechanisms and specific consequences of individual herpesvirus interactions with Rho GTPase signaling may differ. However, some evolutionary distinct but similar general effects on Rho GTPase signaling and the cytoskeleton have also been reported. Examples of these include Rho GTPase-mediated nuclear translocation of virus during entry in a host cell and Rho GTPase-mediated viral cell-to-cell spread during later stages of infection. The current review gives an overview of both general and individual interactions of herpesviruses with Rho GTPase signaling. Molecular Diversity Preservation International (MDPI) 2011-03-24 /pmc/articles/PMC3185701/ /pubmed/21994732 http://dx.doi.org/10.3390/v3040278 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. http://creativecommons.org/licenses/by/3.0 This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Van den Broeke, Céline
Favoreel, Herman W.
Actin’ up: Herpesvirus Interactions with Rho GTPase Signaling
title Actin’ up: Herpesvirus Interactions with Rho GTPase Signaling
title_full Actin’ up: Herpesvirus Interactions with Rho GTPase Signaling
title_fullStr Actin’ up: Herpesvirus Interactions with Rho GTPase Signaling
title_full_unstemmed Actin’ up: Herpesvirus Interactions with Rho GTPase Signaling
title_short Actin’ up: Herpesvirus Interactions with Rho GTPase Signaling
title_sort actin’ up: herpesvirus interactions with rho gtpase signaling
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185701/
https://www.ncbi.nlm.nih.gov/pubmed/21994732
http://dx.doi.org/10.3390/v3040278
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