E2F-associated chromatin modifiers and cell cycle control

被引:136
作者
Blais, Alexandre [3 ]
Dynlacht, Brian D. [1 ,2 ]
机构
[1] NYU, Sch Med, Dept Pathol, New York, NY 10016 USA
[2] NYU, Sch Med, Inst Canc, New York, NY 10016 USA
[3] Univ Ottawa, Fac Med, Dept Microbiol & Immunol, Ottawa Inst Syst Biol & Biochem, Ottawa, ON K1H 8M5, Canada
关键词
D O I
10.1016/j.ceb.2007.10.003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 [细胞生物学]; 090102 [作物遗传育种];
摘要
The E2F family of proteins was identified on the basis of its role in promoting the GO to S phase transition. Research over the past several years has unveiled considerable complexity within the family, with numerous studies pointing to delegation of function for distinct family members. More recent studies highlighted in this review have expanded this picture, suggesting ways in which E2F target gene expression is refined during cell cycle progression by facilitating the acquisition of promoter-specific histone modifications. E2F associated co-activators promote activating histone marks while recruitment of co-repressors associated with E2Fs and the pRB family leads to accretion of inhibitory histone modifications that provoke chromatin compaction.
引用
收藏
页码:658 / 662
页数:5
相关论文
共 32 条
[1]
Pocket protein complexes are recruited to distinct targets in quiescent and proliferating cells [J].
Balciunaite, E ;
Spektor, A ;
Lents, NH ;
Cam, H ;
Riele, HT ;
Scime, A ;
Rudnicki, MA ;
Young, R ;
Dynlacht, BD .
MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (18) :8166-8178
[2]
Role for a Drosophila Myb-containing protein complex in site-specific DNA replication [J].
Beall, EL ;
Manak, JR ;
Zhou, S ;
Bell, M ;
Lipsick, JS ;
Botchan, MR .
NATURE, 2002, 420 (6917) :833-837
[3]
Unbiased location analysis of E2F1-binding sites suggests a widespread role for E2F1 in the human genome [J].
Bieda, M ;
Xu, XQ ;
Singer, MA ;
Green, R ;
Farnham, PJ .
GENOME RESEARCH, 2006, 16 (05) :595-605
[4]
DNA replication control through interaction of E2F-RB and the origin recognition complex [J].
Bosco, G ;
Du, W ;
Orr-Weaver, TL .
NATURE CELL BIOLOGY, 2001, 3 (03) :289-295
[5]
A common set of gene regulatory networks links metabolism and growth inhibition [J].
Cam, H ;
Balciunaite, E ;
Blais, A ;
Spektor, A ;
Scarpulla, RC ;
Young, R ;
Kluger, Y ;
Dynlacht, BD .
MOLECULAR CELL, 2004, 16 (03) :399-411
[6]
Cell cycle-dependent and cell cycle-independent control of transcription by Drosophila E2F/RB pathway [J].
Dimova, DK ;
Stevaux, O ;
Frolov, MV ;
Dyson, NJ .
GENES & DEVELOPMENT, 2003, 17 (18) :2308-2320
[7]
A single-point mutation in HCF causes temperature-sensitive cell-cycle arrest and disrupts VP16 function [J].
Goto, H ;
Motomura, S ;
Wilson, AC ;
Freiman, RN ;
Nakabeppu, Y ;
Fukushima, K ;
Fujishima, M ;
Herr, W ;
Nishimoto, T .
GENES & DEVELOPMENT, 1997, 11 (06) :726-737
[8]
Role for BRG1 in cell cycle control and tumor suppression [J].
Hendricks, KB ;
Shanahan, F ;
Lees, E .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (01) :362-376
[9]
Proteolytic processing is necessary to separate and ensure proper cell growth and cytokinesis functions of HCF-1 [J].
Julien, E ;
Herr, W .
EMBO JOURNAL, 2003, 22 (10) :2360-2369
[10]
FORMATION OF DNA-REPLICATION STRUCTURES IN HERPES-VIRUS INFECTED-CELLS REQUIRES A VIRAL-DNA BINDING-PROTEIN [J].
KOPS, AD ;
KNIPE, DM .
CELL, 1988, 55 (05) :857-868