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Regulation of the HIV-1 promoter by HIF-1α and Vpr proteins

We previously demonstrated the ability of HIV-1 Vpr protein to activate the oxidative stress pathway, thus leading to the induction of the hypoxia inducible factor 1 alpha (HIF-1α). Therefore, we sought to examine the interplay between the two proteins and the impact of HIF-1α activation on HIV-1 tr...

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Autores principales: Deshmane, Satish L, Amini, Shohreh, Sen, Satarupa, Khalili, Kamel, Sawaya, Bassel E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3210103/
https://www.ncbi.nlm.nih.gov/pubmed/22023789
http://dx.doi.org/10.1186/1743-422X-8-477
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author Deshmane, Satish L
Amini, Shohreh
Sen, Satarupa
Khalili, Kamel
Sawaya, Bassel E
author_facet Deshmane, Satish L
Amini, Shohreh
Sen, Satarupa
Khalili, Kamel
Sawaya, Bassel E
author_sort Deshmane, Satish L
collection PubMed
description We previously demonstrated the ability of HIV-1 Vpr protein to activate the oxidative stress pathway, thus leading to the induction of the hypoxia inducible factor 1 alpha (HIF-1α). Therefore, we sought to examine the interplay between the two proteins and the impact of HIF-1α activation on HIV-1 transcription. Using transient transfection assays, we identified the optimal concentration of HIF-1α necessary for the activation of the HIV-1 promoter as well as the domain within HIF-1α responsible for this activation. Our findings indicated that activation of the HIV-1 LTR by Vpr is HIF-1α dependent. Furthermore, we showed that both Vpr and HIF-1α activate the HIV-1 promoter through the GC-rich binding domain within the LTR. Taken together, these data shed more light on the mechanisms used by Vpr to activate the HIV-1 promoter and placed HIF-1α as a major participant in this activation.
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spelling pubmed-32101032011-11-08 Regulation of the HIV-1 promoter by HIF-1α and Vpr proteins Deshmane, Satish L Amini, Shohreh Sen, Satarupa Khalili, Kamel Sawaya, Bassel E Virol J Research We previously demonstrated the ability of HIV-1 Vpr protein to activate the oxidative stress pathway, thus leading to the induction of the hypoxia inducible factor 1 alpha (HIF-1α). Therefore, we sought to examine the interplay between the two proteins and the impact of HIF-1α activation on HIV-1 transcription. Using transient transfection assays, we identified the optimal concentration of HIF-1α necessary for the activation of the HIV-1 promoter as well as the domain within HIF-1α responsible for this activation. Our findings indicated that activation of the HIV-1 LTR by Vpr is HIF-1α dependent. Furthermore, we showed that both Vpr and HIF-1α activate the HIV-1 promoter through the GC-rich binding domain within the LTR. Taken together, these data shed more light on the mechanisms used by Vpr to activate the HIV-1 promoter and placed HIF-1α as a major participant in this activation. BioMed Central 2011-10-24 /pmc/articles/PMC3210103/ /pubmed/22023789 http://dx.doi.org/10.1186/1743-422X-8-477 Text en Copyright ©2011 Deshmane 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 Research
Deshmane, Satish L
Amini, Shohreh
Sen, Satarupa
Khalili, Kamel
Sawaya, Bassel E
Regulation of the HIV-1 promoter by HIF-1α and Vpr proteins
title Regulation of the HIV-1 promoter by HIF-1α and Vpr proteins
title_full Regulation of the HIV-1 promoter by HIF-1α and Vpr proteins
title_fullStr Regulation of the HIV-1 promoter by HIF-1α and Vpr proteins
title_full_unstemmed Regulation of the HIV-1 promoter by HIF-1α and Vpr proteins
title_short Regulation of the HIV-1 promoter by HIF-1α and Vpr proteins
title_sort regulation of the hiv-1 promoter by hif-1α and vpr proteins
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3210103/
https://www.ncbi.nlm.nih.gov/pubmed/22023789
http://dx.doi.org/10.1186/1743-422X-8-477
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