LSD1 cooperates with CTIP2 to promote HIV-1 transcriptional silencing

被引:64
|
作者
Le Douce, Valentin [1 ]
Colin, Laurence [2 ]
Redel, Laetitia [1 ]
Cherrier, Thomas [1 ]
Herbein, Georges [3 ]
Aunis, Dominique [1 ]
Rohr, Olivier [1 ,4 ,5 ]
Van Lint, Carine [2 ]
Schwartz, Christian [1 ,4 ]
机构
[1] Univ Strasbourg, Inst Parasitol, EA4438, Strasbourg, France
[2] Univ Brussels, Mol Virol Lab, Univ Libre Bruxelles, IBMM, B-6041 Gosselies, Belgium
[3] Univ Franche Comte, Dept Virol, UPRES EA Pathogens & Inflammat 3186, CHU Besancon, F-25030 Besancon, France
[4] IUT Louis Pasteur Schiltigheim, F-67300 Schiltigheim, France
[5] Inst Univ France, F-75005 Paris, France
关键词
MONOCYTE-MACROPHAGE LINEAGE; HISTONE H3 LYSINE-4; GENE-EXPRESSION; MICROGLIAL CELLS; CHROMATIN MODIFICATIONS; NUCLEAR RECEPTORS; METHYLATION; LATENCY; COMPASS; COMPLEX;
D O I
10.1093/nar/gkr857
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
Microglial cells are the main HIV-1 targets in the central nervous system (CNS) and constitute an important reservoir of latently infected cells. Establishment and persistence of these reservoirs rely on the chromatin structure of the integrated proviruses. We have previously demonstrated that the cellular cofactor CTIP2 forces heterochromatin formation and HIV-1 gene silencing by recruiting HDAC and HMT activities at the integrated viral promoter. In the present work, we report that the histone demethylase LSD1 represses HIV-1 transcription and viral expression in a synergistic manner with CTIP2. We show that recruitment of LSD1 at the HIV-1 proximal promoter is associated with both H3K4me3 and H3K9me3 epigenetic marks. Finally, our data suggest that LSD1-induced H3K4 trimethylation is linked to hSET1 recruitment at the integrated provirus.
引用
收藏
页码:1904 / 1915
页数:12
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