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CHD1 and CHD2 are positive regulators of HIV-1 gene expression

BACKGROUND: Retroviruses encode a very limited number of proteins and therefore must exploit a wide variety of host proteins for completion of their lifecycle. METHODS: We performed an insertional mutagenesis screen to identify novel cellular regulators of retroviral replication. RESULTS: This appro...

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Detalles Bibliográficos
Autores principales: Rodgers, Melissa J, Banks, David J, Bradley, Kenneth A, Young, John AT
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4283154/
https://www.ncbi.nlm.nih.gov/pubmed/25297984
http://dx.doi.org/10.1186/1743-422X-11-180
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author Rodgers, Melissa J
Banks, David J
Bradley, Kenneth A
Young, John AT
author_facet Rodgers, Melissa J
Banks, David J
Bradley, Kenneth A
Young, John AT
author_sort Rodgers, Melissa J
collection PubMed
description BACKGROUND: Retroviruses encode a very limited number of proteins and therefore must exploit a wide variety of host proteins for completion of their lifecycle. METHODS: We performed an insertional mutagenesis screen to identify novel cellular regulators of retroviral replication. RESULTS: This approach identified the ATP-dependent chromatin remodeler, chromodomain helicase DNA-binding protein 2 (CHD2), as well as the highly related CHD1 protein, as positive regulators of both MLV and HIV-1 replication in rodent and human cells. RNAi knockdown of either CHD2 or the related CHD1 protein, in human cells resulted in a block to infection by HIV-1, specifically at the level of transcription. CONCLUSIONS: These results demonstrate that CHD1 and CHD2 can act as positive regulators of HIV-1 gene expression.
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spelling pubmed-42831542015-01-06 CHD1 and CHD2 are positive regulators of HIV-1 gene expression Rodgers, Melissa J Banks, David J Bradley, Kenneth A Young, John AT Virol J Research BACKGROUND: Retroviruses encode a very limited number of proteins and therefore must exploit a wide variety of host proteins for completion of their lifecycle. METHODS: We performed an insertional mutagenesis screen to identify novel cellular regulators of retroviral replication. RESULTS: This approach identified the ATP-dependent chromatin remodeler, chromodomain helicase DNA-binding protein 2 (CHD2), as well as the highly related CHD1 protein, as positive regulators of both MLV and HIV-1 replication in rodent and human cells. RNAi knockdown of either CHD2 or the related CHD1 protein, in human cells resulted in a block to infection by HIV-1, specifically at the level of transcription. CONCLUSIONS: These results demonstrate that CHD1 and CHD2 can act as positive regulators of HIV-1 gene expression. BioMed Central 2014-10-08 /pmc/articles/PMC4283154/ /pubmed/25297984 http://dx.doi.org/10.1186/1743-422X-11-180 Text en © Rodgers et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Rodgers, Melissa J
Banks, David J
Bradley, Kenneth A
Young, John AT
CHD1 and CHD2 are positive regulators of HIV-1 gene expression
title CHD1 and CHD2 are positive regulators of HIV-1 gene expression
title_full CHD1 and CHD2 are positive regulators of HIV-1 gene expression
title_fullStr CHD1 and CHD2 are positive regulators of HIV-1 gene expression
title_full_unstemmed CHD1 and CHD2 are positive regulators of HIV-1 gene expression
title_short CHD1 and CHD2 are positive regulators of HIV-1 gene expression
title_sort chd1 and chd2 are positive regulators of hiv-1 gene expression
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4283154/
https://www.ncbi.nlm.nih.gov/pubmed/25297984
http://dx.doi.org/10.1186/1743-422X-11-180
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