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

Autor: Mark Leid, Sylvette Chasserot-Golaz, Olivier Rohr, Laetitia Redel, Céline Marban, Stella Suzanne, Evelyne Schaeffer, Dominique Lecestre, Dominique Aunis, Carine Van Lint
Přispěvatelé: Institut de Recherche sur les Maladies Virales et Hépatiques (IVH), Université de Strasbourg (UNISTRA)-Institut National de la Santé et de la Recherche Médicale (INSERM), Biomatériaux et Bioingénierie (BB), Université de Strasbourg (UNISTRA)-Matériaux et nanosciences d'Alsace (FMNGE), Institut de Chimie du CNRS (INC)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM), Institut des Neurosciences Cellulaires et Intégratives (INCI), Université Louis Pasteur - Strasbourg I-Centre National de la Recherche Scientifique (CNRS), Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS), Immunopathologie et chimie thérapeutique (ICT), Institut de biologie moléculaire et cellulaire (IBMC), Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS), Dynamique des interactions Hôte pathogène, Université de Strasbourg (UNISTRA), P30 ES000210, Université de Strasbourg (UNISTRA)-Matériaux et nanosciences d'Alsace, Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Institut National de la Santé et de la Recherche Médicale (INSERM), Institut des Neurosciences Cellulaires et Intégratives, Centre National de la Recherche Scientifique (CNRS), Université de Strasbourg (UNISTRA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Matériaux et nanosciences d'Alsace, Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université de Strasbourg (UNISTRA)-Université de Haute-Alsace (UHA) Mulhouse - Colmar (Université de Haute-Alsace (UHA))-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
Jazyk: francouzština
Rok vydání: 2005
Předmět:
Receptors
Steroid

Repressor Proteins -- analysis
Transcription
Genetic

analysis
physiology
Chromosomal Proteins
Non-Histone

Response element
DNA-Binding Proteins -- physiology
Virus Replication
Receptors
Steroid -- antagonists & inhibitors

0302 clinical medicine
Sciences du Vivant [q-bio]/Biologie cellulaire
genetics
Chromosomal Proteins
Non-Histone -- analysis

antagonists & inhibitors
chemistry
0303 health sciences
General transcription factor
Nuclear Proteins
DNA-Binding Proteins -- analysis
TCF4
Sciences bio-médicales et agricoles
3. Good health
DNA-Binding Proteins
030220 oncology & carcinogenesis
TAF2
Cell Nucleus Structures -- chemistry
Microglia
Sp1 Transcription Factor -- antagonists & inhibitors
Carrier Proteins -- physiology
Transcription Factors -- antagonists & inhibitors
Gene Expression Regulation
Viral

Sp1 Transcription Factor
Repressor Proteins -- physiology
E-box
DNA-Binding Proteins -- antagonists & inhibitors
[SDV.BC]Life Sciences [q-bio]/Cellular Biology
Biology
Article
Cell Line
03 medical and health sciences
HIV-1 -- physiology
Sp3 transcription factor
HIV-1 -- genetics
Genetics
Humans
Enhancer
Sp1 Transcription Factor -- chemistry
030304 developmental biology
HIV Long Terminal Repeat
Tumor Suppressor Proteins
Promoter
DNA-Binding Proteins -- chemistry
Microglia -- virology
Molecular biology
Transcription Factors -- analysis
Cell Nucleus Structures
Protein Structure
Tertiary

Repressor Proteins
Transcription Factors -- chemistry
COUP Transcription Factors
Nuclear Proteins -- physiology
Receptors
Steroid -- analysis

Chromobox Protein Homolog 5
metabolism
virology
HIV-1
Microglia -- metabolism
Carrier Proteins
Receptors
Steroid -- chemistry

Transcription Factors
Sp1 Transcription Factor -- analysis
Zdroj: Nucleic Acids Research
Nucleic Acids Research, Oxford University Press, 2005, 33 (7), ⟨10.1093/nar/gki529⟩
Nucleic acids research, 33 (7
ISSN: 0305-1048
1362-4962
DOI: 10.1093/nar/gki529⟩
Popis: 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 Hp1alpha, 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.
Journal Article
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, P.H.S.
SCOPUS: ar.j
info:eu-repo/semantics/published
Databáze: OpenAIRE