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Restriction of Retroviral Replication by Tetherin/BST-2

Tetherin/BST-2 is an important host restriction factor that limits the replication of HIV and other enveloped viruses. Tetherin is a type II membrane glycoprotein with a very unusual domain structure that allows it to engage budding virions and retain them on the plasma membrane of infected cells. F...

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Detalles Bibliográficos
Autores principales: Hammonds, Jason, Wang, Jaang-Jiun, Spearman, Paul
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3395152/
https://www.ncbi.nlm.nih.gov/pubmed/22811908
http://dx.doi.org/10.1155/2012/424768
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author Hammonds, Jason
Wang, Jaang-Jiun
Spearman, Paul
author_facet Hammonds, Jason
Wang, Jaang-Jiun
Spearman, Paul
author_sort Hammonds, Jason
collection PubMed
description Tetherin/BST-2 is an important host restriction factor that limits the replication of HIV and other enveloped viruses. Tetherin is a type II membrane glycoprotein with a very unusual domain structure that allows it to engage budding virions and retain them on the plasma membrane of infected cells. Following the initial report identifying tetherin as the host cell factor targeted by the HIV-1 Vpu gene, knowledge of the molecular, structural, and cellular biology of tetherin has rapidly advanced. This paper summarizes the discovery and impact of tetherin biology on the HIV field, with a focus on recent advances in understanding its structure and function. The relevance of tetherin to replication and spread of other retroviruses is also reviewed. Tetherin is a unique host restriction factor that is likely to continue to provide new insights into host-virus interactions and illustrates well the varied ways by which host organisms defend against viral pathogens.
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spelling pubmed-33951522012-07-18 Restriction of Retroviral Replication by Tetherin/BST-2 Hammonds, Jason Wang, Jaang-Jiun Spearman, Paul Mol Biol Int Review Article Tetherin/BST-2 is an important host restriction factor that limits the replication of HIV and other enveloped viruses. Tetherin is a type II membrane glycoprotein with a very unusual domain structure that allows it to engage budding virions and retain them on the plasma membrane of infected cells. Following the initial report identifying tetherin as the host cell factor targeted by the HIV-1 Vpu gene, knowledge of the molecular, structural, and cellular biology of tetherin has rapidly advanced. This paper summarizes the discovery and impact of tetherin biology on the HIV field, with a focus on recent advances in understanding its structure and function. The relevance of tetherin to replication and spread of other retroviruses is also reviewed. Tetherin is a unique host restriction factor that is likely to continue to provide new insights into host-virus interactions and illustrates well the varied ways by which host organisms defend against viral pathogens. Hindawi Publishing Corporation 2012 2012-07-02 /pmc/articles/PMC3395152/ /pubmed/22811908 http://dx.doi.org/10.1155/2012/424768 Text en Copyright © 2012 Jason Hammonds et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Hammonds, Jason
Wang, Jaang-Jiun
Spearman, Paul
Restriction of Retroviral Replication by Tetherin/BST-2
title Restriction of Retroviral Replication by Tetherin/BST-2
title_full Restriction of Retroviral Replication by Tetherin/BST-2
title_fullStr Restriction of Retroviral Replication by Tetherin/BST-2
title_full_unstemmed Restriction of Retroviral Replication by Tetherin/BST-2
title_short Restriction of Retroviral Replication by Tetherin/BST-2
title_sort restriction of retroviral replication by tetherin/bst-2
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3395152/
https://www.ncbi.nlm.nih.gov/pubmed/22811908
http://dx.doi.org/10.1155/2012/424768
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