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Centrosome and retroviruses: The dangerous liaisons

Centrosomes are the major microtubule organizing structures in vertebrate cells. They localize in close proximity to the nucleus for the duration of interphase and play major roles in numerous cell functions. Consequently, any deficiency in centrosome function or number may lead to genetic instabili...

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Detalles Bibliográficos
Autores principales: Afonso, Philippe V, Zamborlini, Alessia, Saïb, Ali, Mahieux, Renaud
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1855351/
https://www.ncbi.nlm.nih.gov/pubmed/17433108
http://dx.doi.org/10.1186/1742-4690-4-27
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author Afonso, Philippe V
Zamborlini, Alessia
Saïb, Ali
Mahieux, Renaud
author_facet Afonso, Philippe V
Zamborlini, Alessia
Saïb, Ali
Mahieux, Renaud
author_sort Afonso, Philippe V
collection PubMed
description Centrosomes are the major microtubule organizing structures in vertebrate cells. They localize in close proximity to the nucleus for the duration of interphase and play major roles in numerous cell functions. Consequently, any deficiency in centrosome function or number may lead to genetic instability. Several viruses including retroviruses such as, Foamy Virus, HIV-1, JSRV, M-PMV and HTLV-1 have been shown to hamper centrosome functions for their own profit, but the outcomes are very different. Foamy viruses, HIV-1, JSRV, M-PMV and HTLV-1 use the cellular machinery to traffic towards the centrosome during early and/or late stages of the infection. In addition HIV-1 Vpr protein alters the cell-cycle regulation by hijacking centrosome functions. Enthrallingly, HTLV-1 Tax expression also targets the functions of the centrosome, and this event is correlated with centrosome amplification, aneuploidy and transformation.
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spelling pubmed-18553512007-04-25 Centrosome and retroviruses: The dangerous liaisons Afonso, Philippe V Zamborlini, Alessia Saïb, Ali Mahieux, Renaud Retrovirology Review Centrosomes are the major microtubule organizing structures in vertebrate cells. They localize in close proximity to the nucleus for the duration of interphase and play major roles in numerous cell functions. Consequently, any deficiency in centrosome function or number may lead to genetic instability. Several viruses including retroviruses such as, Foamy Virus, HIV-1, JSRV, M-PMV and HTLV-1 have been shown to hamper centrosome functions for their own profit, but the outcomes are very different. Foamy viruses, HIV-1, JSRV, M-PMV and HTLV-1 use the cellular machinery to traffic towards the centrosome during early and/or late stages of the infection. In addition HIV-1 Vpr protein alters the cell-cycle regulation by hijacking centrosome functions. Enthrallingly, HTLV-1 Tax expression also targets the functions of the centrosome, and this event is correlated with centrosome amplification, aneuploidy and transformation. BioMed Central 2007-04-14 /pmc/articles/PMC1855351/ /pubmed/17433108 http://dx.doi.org/10.1186/1742-4690-4-27 Text en Copyright © 2007 Afonso et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Afonso, Philippe V
Zamborlini, Alessia
Saïb, Ali
Mahieux, Renaud
Centrosome and retroviruses: The dangerous liaisons
title Centrosome and retroviruses: The dangerous liaisons
title_full Centrosome and retroviruses: The dangerous liaisons
title_fullStr Centrosome and retroviruses: The dangerous liaisons
title_full_unstemmed Centrosome and retroviruses: The dangerous liaisons
title_short Centrosome and retroviruses: The dangerous liaisons
title_sort centrosome and retroviruses: the dangerous liaisons
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1855351/
https://www.ncbi.nlm.nih.gov/pubmed/17433108
http://dx.doi.org/10.1186/1742-4690-4-27
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