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Vpr and Its Cellular Interaction Partners: R We There Yet?

Vpr is a lentiviral accessory protein that is expressed late during the infection cycle and is packaged in significant quantities into virus particles through a specific interaction with the P6 domain of the viral Gag precursor. Characterization of the physiologically relevant function(s) of Vpr has...

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Detalles Bibliográficos
Autores principales: Fabryova, Helena, Strebel, Klaus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6912716/
https://www.ncbi.nlm.nih.gov/pubmed/31652959
http://dx.doi.org/10.3390/cells8111310
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author Fabryova, Helena
Strebel, Klaus
author_facet Fabryova, Helena
Strebel, Klaus
author_sort Fabryova, Helena
collection PubMed
description Vpr is a lentiviral accessory protein that is expressed late during the infection cycle and is packaged in significant quantities into virus particles through a specific interaction with the P6 domain of the viral Gag precursor. Characterization of the physiologically relevant function(s) of Vpr has been hampered by the fact that in many cell lines, deletion of Vpr does not significantly affect viral fitness. However, Vpr is critical for virus replication in primary macrophages and for viral pathogenesis in vivo. It is generally accepted that Vpr does not have a specific enzymatic activity but functions as a molecular adapter to modulate viral or cellular processes for the benefit of the virus. Indeed, many Vpr interacting factors have been described by now, and the goal of this review is to summarize our current knowledge of cellular proteins targeted by Vpr.
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spelling pubmed-69127162020-01-02 Vpr and Its Cellular Interaction Partners: R We There Yet? Fabryova, Helena Strebel, Klaus Cells Review Vpr is a lentiviral accessory protein that is expressed late during the infection cycle and is packaged in significant quantities into virus particles through a specific interaction with the P6 domain of the viral Gag precursor. Characterization of the physiologically relevant function(s) of Vpr has been hampered by the fact that in many cell lines, deletion of Vpr does not significantly affect viral fitness. However, Vpr is critical for virus replication in primary macrophages and for viral pathogenesis in vivo. It is generally accepted that Vpr does not have a specific enzymatic activity but functions as a molecular adapter to modulate viral or cellular processes for the benefit of the virus. Indeed, many Vpr interacting factors have been described by now, and the goal of this review is to summarize our current knowledge of cellular proteins targeted by Vpr. MDPI 2019-10-24 /pmc/articles/PMC6912716/ /pubmed/31652959 http://dx.doi.org/10.3390/cells8111310 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Fabryova, Helena
Strebel, Klaus
Vpr and Its Cellular Interaction Partners: R We There Yet?
title Vpr and Its Cellular Interaction Partners: R We There Yet?
title_full Vpr and Its Cellular Interaction Partners: R We There Yet?
title_fullStr Vpr and Its Cellular Interaction Partners: R We There Yet?
title_full_unstemmed Vpr and Its Cellular Interaction Partners: R We There Yet?
title_short Vpr and Its Cellular Interaction Partners: R We There Yet?
title_sort vpr and its cellular interaction partners: r we there yet?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6912716/
https://www.ncbi.nlm.nih.gov/pubmed/31652959
http://dx.doi.org/10.3390/cells8111310
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