Hu Qianghua, Lu Jing-Fang, Luo Rong, Sen Subrata, Maity Sankar N
Department of Molecular Genetics, The University of Texas M. D. Anderson Cancer center, Houston, TX 77030, USA.
Nucleic Acids Res. 2006;34(21):6272-85. doi: 10.1093/nar/gkl801. Epub 2006 Nov 10.
Previous studies showed that binding of the CBF/NF-Y (CBF) transcription factor to cellular promoters is essential for cell proliferation. This observation prompted us to investigate the function of CBF in relation to cell cycle progression and in cell-cycle-regulated transcription. In this study, we used a tetracycline-inducible adenoviral vector to express a truncated CBF-B subunit, Bdbd, lacking a transcription activation domain in various mammalian cell lines. The Bdbd polypeptide interacts with cellular CBF-A/CBF-C and binds to promoters containing CBF-binding sites. Interestingly, expression of Bdbd in various mammalian cells resulted in the inhibition of cell proliferation and specific cell cycle arrest at G2/M phase. Gene expression analysis demonstrated that the expression of Bdbd strongly suppressed cell cycle-dependent transcription activation of Cyclin B1, Aurora A and CDK1 genes, key regulators for cell cycle progression at G2/M phase. Chromatin immunoprecipitation analysis showed that Bdbd significantly inhibited binding of TATA-binding protein, TBP to both Cyclin B1 and Aurora A promoters, but did not inhibit binding of E2F3 activator to Cyclin B1 promoter. This study suggested that the activation domain of CBF-B plays an essential role in the transcription activation of Cyclin B1 and Aurora A genes at G2/M phase, thus regulating cell cycle progression at G2/M phase.
先前的研究表明,CBF/NF-Y(CBF)转录因子与细胞启动子的结合对细胞增殖至关重要。这一观察结果促使我们研究CBF在细胞周期进程以及细胞周期调控转录方面的功能。在本研究中,我们使用四环素诱导型腺病毒载体在多种哺乳动物细胞系中表达截短的CBF-B亚基Bdbd,该亚基缺乏转录激活结构域。Bdbd多肽与细胞内的CBF-A/CBF-C相互作用,并与含有CBF结合位点的启动子结合。有趣的是,在多种哺乳动物细胞中表达Bdbd会导致细胞增殖受到抑制,并在G2/M期出现特异性细胞周期阻滞。基因表达分析表明,Bdbd的表达强烈抑制了细胞周期蛋白B1(Cyclin B1)、极光激酶A(Aurora A)和细胞周期蛋白依赖性激酶1(CDK1)基因的细胞周期依赖性转录激活,这些基因是G2/M期细胞周期进程的关键调节因子。染色质免疫沉淀分析表明,Bdbd显著抑制了TATA结合蛋白(TBP)与Cyclin B1和Aurora A启动子的结合,但不抑制E2F3激活剂与Cyclin B1启动子的结合。本研究表明,CBF-B的激活结构域在G2/M期对Cyclin B1和Aurora A基因的转录激活中起关键作用,从而调控G2/M期的细胞周期进程。