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COUP-TF interacting protein 2 represses the initial phase of HIV-1 gene transcription in human microglial cells

Human immunodeficiency virus type 1 (HIV-1) gene transcription is characterized by two temporally distinct phases. While the initial phase relies solely on cellular transcription factors, the subsequent phase is activated by the viral Tat transactivator. We have previously reported that the subseque...

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Autores principales: Marban, Céline, Redel, Laetitia, Suzanne, Stella, Van Lint, Carine, Lecestre, Dominique, Chasserot-Golaz, Sylvette, Leid, Mark, Aunis, Dominique, Schaeffer, Evelyne, Rohr, Olivier
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2005
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1084325/
https://www.ncbi.nlm.nih.gov/pubmed/15849318
http://dx.doi.org/10.1093/nar/gki529
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author Marban, Céline
Redel, Laetitia
Suzanne, Stella
Van Lint, Carine
Lecestre, Dominique
Chasserot-Golaz, Sylvette
Leid, Mark
Aunis, Dominique
Schaeffer, Evelyne
Rohr, Olivier
author_facet Marban, Céline
Redel, Laetitia
Suzanne, Stella
Van Lint, Carine
Lecestre, Dominique
Chasserot-Golaz, Sylvette
Leid, Mark
Aunis, Dominique
Schaeffer, Evelyne
Rohr, Olivier
author_sort Marban, Céline
collection PubMed
description Human immunodeficiency virus type 1 (HIV-1) gene transcription is characterized by two temporally distinct phases. While the initial phase relies solely on cellular transcription factors, the subsequent phase is activated by the viral Tat transactivator. We have previously reported that the subsequent phase of viral gene transcription can be repressed by the chicken ovalbumin upstream promoter transcription factor (COUP-TF)-interacting protein 2 (CTIP2) in human microglial cells [O. Rohr, D. Lecestre, S. Chasserot-Golaz, C. Marban, D. Avram, D. Aunis, M. Leid and E. Schaeffer (2003), J. Virol., 77, 5415–5427]. Here, we demonstrate that CTIP proteins also repress the initial phase of HIV-1 gene transcription, mainly supported by the cellular transcription factors Sp1 and COUP-TF in microglial cells. We report that CTIP2 represses Sp1- and COUP-TF-mediated activation of HIV-1 gene transcription and viral replication as a result of physical interactions with COUP-TF and Sp1 in microglial nuclei. Using laser confocal microscopy CTIP2 was found to colocalize with Sp1, COUP-TF and the heterochromatin-associated protein Hp1α, which is mainly detected in transcriptionally repressed heterochromatic region. Moreover, we describe that CTIP2 can be recruited to the HIV-1 promoter via its association with Sp1 bound to the GC-box sequences of the long terminal repeat (LTR). Since our findings demonstrate that CTIP2 interacts with the HIV-1 proximal promoter, it is likely that CTIP2 promotes HIV-1 gene silencing by forcing transcriptionally repressed heterochromatic environment to the viral LTR region.
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spelling pubmed-10843252005-04-22 COUP-TF interacting protein 2 represses the initial phase of HIV-1 gene transcription in human microglial cells Marban, Céline Redel, Laetitia Suzanne, Stella Van Lint, Carine Lecestre, Dominique Chasserot-Golaz, Sylvette Leid, Mark Aunis, Dominique Schaeffer, Evelyne Rohr, Olivier Nucleic Acids Res Article Human immunodeficiency virus type 1 (HIV-1) gene transcription is characterized by two temporally distinct phases. While the initial phase relies solely on cellular transcription factors, the subsequent phase is activated by the viral Tat transactivator. We have previously reported that the subsequent phase of viral gene transcription can be repressed by the chicken ovalbumin upstream promoter transcription factor (COUP-TF)-interacting protein 2 (CTIP2) in human microglial cells [O. Rohr, D. Lecestre, S. Chasserot-Golaz, C. Marban, D. Avram, D. Aunis, M. Leid and E. Schaeffer (2003), J. Virol., 77, 5415–5427]. Here, we demonstrate that CTIP proteins also repress the initial phase of HIV-1 gene transcription, mainly supported by the cellular transcription factors Sp1 and COUP-TF in microglial cells. We report that CTIP2 represses Sp1- and COUP-TF-mediated activation of HIV-1 gene transcription and viral replication as a result of physical interactions with COUP-TF and Sp1 in microglial nuclei. Using laser confocal microscopy CTIP2 was found to colocalize with Sp1, COUP-TF and the heterochromatin-associated protein Hp1α, which is mainly detected in transcriptionally repressed heterochromatic region. Moreover, we describe that CTIP2 can be recruited to the HIV-1 promoter via its association with Sp1 bound to the GC-box sequences of the long terminal repeat (LTR). Since our findings demonstrate that CTIP2 interacts with the HIV-1 proximal promoter, it is likely that CTIP2 promotes HIV-1 gene silencing by forcing transcriptionally repressed heterochromatic environment to the viral LTR region. Oxford University Press 2005 2005-04-22 /pmc/articles/PMC1084325/ /pubmed/15849318 http://dx.doi.org/10.1093/nar/gki529 Text en © The Author 2005. Published by Oxford University Press. All rights reserved
spellingShingle Article
Marban, Céline
Redel, Laetitia
Suzanne, Stella
Van Lint, Carine
Lecestre, Dominique
Chasserot-Golaz, Sylvette
Leid, Mark
Aunis, Dominique
Schaeffer, Evelyne
Rohr, Olivier
COUP-TF interacting protein 2 represses the initial phase of HIV-1 gene transcription in human microglial cells
title COUP-TF interacting protein 2 represses the initial phase of HIV-1 gene transcription in human microglial cells
title_full COUP-TF interacting protein 2 represses the initial phase of HIV-1 gene transcription in human microglial cells
title_fullStr COUP-TF interacting protein 2 represses the initial phase of HIV-1 gene transcription in human microglial cells
title_full_unstemmed COUP-TF interacting protein 2 represses the initial phase of HIV-1 gene transcription in human microglial cells
title_short COUP-TF interacting protein 2 represses the initial phase of HIV-1 gene transcription in human microglial cells
title_sort coup-tf interacting protein 2 represses the initial phase of hiv-1 gene transcription in human microglial cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1084325/
https://www.ncbi.nlm.nih.gov/pubmed/15849318
http://dx.doi.org/10.1093/nar/gki529
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