Cell cycle regulation of the murine cdc25B promoter -: Essential role for nuclear factor-Y and a proximal repressor element

被引:37
作者
Körner, K [1 ]
Jérôme, V [1 ]
Schmidt, T [1 ]
Müller, R [1 ]
机构
[1] Univ Marburg, Inst Mol Biol & Tumorforsch, D-35033 Marburg, Germany
关键词
D O I
10.1074/jbc.M008696200
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
Expression of the cdc25B gene is up-regulated late during cell cycle progression (S/G(2)). We have cloned the murine cdc25B promoter to identify elements involved in transcriptional regulation. A detailed structure-function analysis led to the identification of several elements that are located upstream of a canonical Inr motif at the site of transcription initiation and are involved in transcriptional activation and regulation. Activation of the promoter is largely mediated by NF-Y and Sp1/3 interacting with one and four proximal binding sites, respectively. In addition, NF-Y plays an essential role in cell cycle regulation in conjunction with a repressor element (cell cycle-regulated repressor) located similar to 30 nucleotides upstream of the putative Inr element and overlapping a consensus TATA motif. The cell cycle-regulated repressor is unrelated to the previously described cell cycle-regulated repressor elements. Taken together, our observations suggest that expression of the cdc25B gene is controlled through a novel mechanism of cell cycle-regulated transcription.
引用
收藏
页码:9662 / 9669
页数:8
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