Liu Hanshao, Hew Hoi Chin, Lu Zheng-Guang, Yamaguchi Tomoko, Miki Yoshio, Yoshida Kiyotsugu
Department of Molecular Genetics, Medical Research Institute, Tokyo Medical and Dental University, Tokyo 113-8510, Japan.
Biochem J. 2009 Aug 27;422(3):543-51. doi: 10.1042/BJ20090342.
Transcriptional regulation of the p53 tumour suppressor gene plays an important role in the control of the expression of various target genes involved in the DNA damage response. However, the molecular basis of this regulation remains obscure. In the present study we demonstrate that RREB-1 (Ras-responsive-element-binding protein-1) efficiently binds to the p53 promoter via the p53 core promoter element and transactivates p53 expression. Silencing of RREB-1 significantly reduces p53 expression at both the mRNA and the protein levels. Notably, disruption of RREB-1-mediated p53 transcription suppresses the expression of the p53 target genes. We also show that, upon exposure to genotoxic stress, RREB-1 controls apoptosis in a p53-dependent manner. These findings provide evidence that RREB-1 participates in modulating p53 transcription in response to DNA damage.
p53肿瘤抑制基因的转录调控在控制参与DNA损伤反应的各种靶基因的表达中起着重要作用。然而,这种调控的分子基础仍然不清楚。在本研究中,我们证明RREB-1(Ras反应元件结合蛋白-1)通过p53核心启动子元件有效结合p53启动子并反式激活p53表达。RREB-1的沉默在mRNA和蛋白质水平上均显著降低p53表达。值得注意的是,RREB-1介导的p53转录的破坏抑制了p53靶基因的表达。我们还表明,在暴露于基因毒性应激时,RREB-1以p53依赖的方式控制细胞凋亡。这些发现提供了证据,证明RREB-1参与响应DNA损伤调节p53转录。