The chromatin remodeller CHD8 is required for E2F-dependent transcription activation of S-phase genes

被引:59
|
作者
Subtil-Rodriguez, Alicia [1 ]
Vazquez-Chavez, Elena [1 ]
Ceballos-Chavez, Maria [1 ]
Rodriguez-Paredes, Manuel [2 ]
Martin-Subero, Jose I. [3 ]
Esteller, Manel [2 ]
Reyes, Jose C. [1 ]
机构
[1] CSIC, Dept Mol Biol, Ctr Andaluz Biol Mol & Med Regenerat CABIMER, Seville 41092, Spain
[2] Bellvitge Biomed Res Inst, Canc Epigenet & Biol Program, Barcelona, Spain
[3] Univ Barcelona, Dept Anat Pathol Pharmacol & Microbiol, E-08007 Barcelona, Spain
关键词
HISTONE H1 RECRUITMENT; RNA-POLYMERASE-II; EXPRESSION; PROTEIN; CYCLE; FAMILY; ASSOCIATION; ELONGATION; COMPLEXES; INTERACTS;
D O I
10.1093/nar/gkt1161
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
The precise regulation of S-phase-specific genes is critical for cell proliferation. How the repressive chromatin configuration mediated by the retinoblastoma protein and repressor E2F factors changes at the G1/S transition to allow transcription activation is unclear. Here we show ChIP-on-chip studies that reveal that the chromatin remodeller CHD8 binds similar to 2000 transcriptionally active promoters. The spectrum of CHD8 target genes was enriched in E2F-dependent genes. We found that CHD8 binds E2F-dependent promoters at the G1/S transition but not in quiescent cells. Consistently, CHD8 was required for G1/S-specific expression of these genes and for cell cycle re-entry on serum stimulation of quiescent cells. We also show that CHD8 interacts with E2F1 and, importantly, loading of E2F1 and E2F3, but not E2F4, onto S-specific promoters, requires CHD8. However, CHD8 recruiting is independent of these factors. Recruiting of MLL histone methyltransferase complexes to S-specific promoters was also severely impaired in the absence of CHD8. Furthermore, depletion of CHD8 abolished E2F1 overexpression-dependent S-phase stimulation of serum-starved cells, highlighting the essential role of CHD8 in E2F-dependent transcription activation.
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收藏
页码:2185 / 2196
页数:12
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