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Host restriction factors in retroviral infection: promises in virus-host interaction

Retroviruses have an intricate life cycle. There is much to be learned from studying retrovirus-host interactions. Among retroviruses, the primate lentiviruses have one of the more complex genome structures with three categories of viral genes: structural, regulatory, and accessory genes. Over time,...

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Detalles Bibliográficos
Autores principales: Zheng, Yong-Hui, Jeang, Kuan-Teh, Tokunaga, Kenzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3549941/
https://www.ncbi.nlm.nih.gov/pubmed/23254112
http://dx.doi.org/10.1186/1742-4690-9-112
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author Zheng, Yong-Hui
Jeang, Kuan-Teh
Tokunaga, Kenzo
author_facet Zheng, Yong-Hui
Jeang, Kuan-Teh
Tokunaga, Kenzo
author_sort Zheng, Yong-Hui
collection PubMed
description Retroviruses have an intricate life cycle. There is much to be learned from studying retrovirus-host interactions. Among retroviruses, the primate lentiviruses have one of the more complex genome structures with three categories of viral genes: structural, regulatory, and accessory genes. Over time, we have gained increasing understanding of the lentivirus life cycle from studying host factors that support virus replication. Similarly, studies on host restriction factors that inhibit viral replication have also made significant contributions to our knowledge. Here, we review recent progress on the rapidly growing field of restriction factors, focusing on the antiretroviral activities of APOBEC3G, TRIM5, tetherin, SAMHD1, MOV10, and cellular microRNAs (miRNAs), and the counter-activities of Vif, Vpu, Vpr, Vpx, and Nef.
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spelling pubmed-35499412013-01-24 Host restriction factors in retroviral infection: promises in virus-host interaction Zheng, Yong-Hui Jeang, Kuan-Teh Tokunaga, Kenzo Retrovirology Review Retroviruses have an intricate life cycle. There is much to be learned from studying retrovirus-host interactions. Among retroviruses, the primate lentiviruses have one of the more complex genome structures with three categories of viral genes: structural, regulatory, and accessory genes. Over time, we have gained increasing understanding of the lentivirus life cycle from studying host factors that support virus replication. Similarly, studies on host restriction factors that inhibit viral replication have also made significant contributions to our knowledge. Here, we review recent progress on the rapidly growing field of restriction factors, focusing on the antiretroviral activities of APOBEC3G, TRIM5, tetherin, SAMHD1, MOV10, and cellular microRNAs (miRNAs), and the counter-activities of Vif, Vpu, Vpr, Vpx, and Nef. BioMed Central 2012-12-20 /pmc/articles/PMC3549941/ /pubmed/23254112 http://dx.doi.org/10.1186/1742-4690-9-112 Text en Copyright ©2012 Zheng 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
Zheng, Yong-Hui
Jeang, Kuan-Teh
Tokunaga, Kenzo
Host restriction factors in retroviral infection: promises in virus-host interaction
title Host restriction factors in retroviral infection: promises in virus-host interaction
title_full Host restriction factors in retroviral infection: promises in virus-host interaction
title_fullStr Host restriction factors in retroviral infection: promises in virus-host interaction
title_full_unstemmed Host restriction factors in retroviral infection: promises in virus-host interaction
title_short Host restriction factors in retroviral infection: promises in virus-host interaction
title_sort host restriction factors in retroviral infection: promises in virus-host interaction
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3549941/
https://www.ncbi.nlm.nih.gov/pubmed/23254112
http://dx.doi.org/10.1186/1742-4690-9-112
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