Regulation of cdc2 gene expression by the upstream stimulatory factors (USFs)

被引:25
作者
North, S
Espanel, X
Bantignies, F
Viollet, B
Vallet, V
Jalinot, P
Brun, G
Gillet, G
机构
[1] CNRS, Inst Biol & Chim Prot, UPR 412, F-69367 Lyon 07, France
[2] CHU Cochin Port Royal, INSERM, U129, Unite Rech Genet & Pathol Mol, F-75014 Paris, France
[3] Ecole Normale Super Lyon, UMR CNRS 49, Res Grp, Mol & Cellular Biol Lab, F-69364 Lyon 07, France
[4] Ecole Normale Super Lyon, UMR CNRS 49, F-69364 Lyon 07, France
关键词
cell cycle; differentiation; retina; cdc2; USF;
D O I
10.1038/sj.onc.1202506
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
cdc2 gene expression is under the control of multiple factors. Although E2F/DP proteins have been reported to play a central role, they cannot account for all aspects of the fine modulation of cdc2 gene expression during cell cycle and embryonic development. To characterize the transcription factors that control cdc2 gene expression during nerve cell differentiation in avians, we have previously cloned the quail cdc2 gene promoter region. We had identified an octamer (CAGGTGGC) containing an E-box, which has important activity in regulating cdc2 transcription. Using lit vivo genomic footprinting experiments, we show here that this motif, currently named TG, is the target of binding proteins at different stages of neuroretina development, confirming its importance as a regulatory response element for cdc2 gene expression. A subset of Helix-Loop-Helix family of transcription factors, known as Upstream Stimulatory Factors (USFs) specifically bind to this sequence as dimers, Moreover, our results indicate that USFs transactivate the promoter of cdc2 via the IG motif, These data may help to better understand the mechanisms that control cell division in differentiating nerve cells.
引用
收藏
页码:1945 / 1955
页数:11
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