p21WAF1 gene promoter is epigenetically silenced by CTIP2 and SUV39H1

被引:94
作者
Cherrier, T. [1 ]
Suzanne, S. [1 ]
Redel, L. [1 ]
Calao, M. [8 ]
Marban, C. [1 ]
Samah, B. [2 ]
Mukerjee, R. [3 ]
Schwartz, C. [1 ]
Gras, G. [2 ]
Sawaya, B. E. [3 ]
Zeichner, S. L. [4 ,5 ,6 ,7 ]
Aunis, D. [1 ]
Van Lint, C. [8 ]
Rohr, O. [1 ,9 ]
机构
[1] Univ Strasbourg, INSERM, Inst Virol, U575, F-67000 Strasbourg, France
[2] Serv Neurovirol, CEA, UMRE 01, Fontenay Aux Roses, France
[3] Temple Univ, Dept Neurol, Sch Med, Mol Virol Lab, Philadelphia, PA 19122 USA
[4] Childrens Natl Med Ctr, Washington, DC 20010 USA
[5] George Washington Univ, Childrens Res Inst, Dept Pediat & Microbiol, Washington, DC USA
[6] George Washington Univ, Childrens Res Inst, Dept Immunol, Washington, DC USA
[7] George Washington Univ, Childrens Res Inst, Dept Trop Med, Washington, DC USA
[8] Univ Libre Bruxelles, Inst Biol & Med Mol, Mol Virol Lab, Gosselies, Belgium
[9] IUT Louis Pasteur Schiltigheim, Schiltigheim, France
关键词
CTIP2; p21(WAF1); SUV39H1; HIV-1; CELL-CYCLE ARREST; HISTONE DEACETYLASE INHIBITORS; MICROGLIAL CELLS; T-LYMPHOCYTES; HIV-1; VPR; TRANSCRIPTIONAL ACTIVATION; P21/WAF1/CIP1; GENE; DNA-REPLICATION; NURD COMPLEX; IN-VIVO;
D O I
10.1038/onc.2009.193
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mainly regulated at the transcriptional level, the cellular cyclin-dependent kinase inhibitor, CDKN1A/p21(WAF1) (p21), is a major cell cycle regulator of the response to DNA damage, senescence and tumor suppression. Here, we report that COUP-TF-interacting protein 2 (CTIP2), recruited to the p21 gene promoter, silenced p21 gene transcription through interactions with histone deacetylases and methyltransferases. Importantly, treatment with the specific SUV39H1 inhibitor, chaetocin, repressed histone H3 lysine 9 trimethylation at the p21 gene promoter, stimulated p21 gene expression and induced cell cycle arrest. In addition, CTIP2 and SUV39H1 were recruited to the silenced p21 gene promoter to cooperatively inhibit p21 gene transcription. Induction of p21(WAF1) gene upon human immunodeficiency virus 1 (HIV-1) infection benefits viral expression in macrophages. Here, we report that CTIP2 further abolishes Vpr-mediated stimulation of p21, thereby indirectly contributing to HIV-1 latency. Altogether, our results suggest that CTIP2 is a constitutive p21 gene suppressor that cooperates with SUV39H1 and histone methylation to silence the p21 gene transcription. Oncogene (2009) 28, 3380-3389; doi: 10.1038/onc.2009.193; published online 6 July 2009
引用
收藏
页码:3380 / 3389
页数:10
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