Department of Medical Oncology, Jinling Hospital, Medical School of Nanjing University, Nanjing 210002, China.
Duke Cancer Institute, Duke University School of Medicine, USA.
Biochem Biophys Res Commun. 2014 Jan 24;443(4):1239-44. doi: 10.1016/j.bbrc.2013.12.124. Epub 2014 Jan 3.
The promoter of p53 induced gene 3 (PIG3) contains a variable number of tandem repeats (VNTRs) of pentanucleotides (TGYCC)n that is known as a p53 binding site. In this study, we investigated whether other potential molecules could bind to this PIG3 promoter (TGYCC)n motif. Ligand-chromatography combined with liquid chromatography-tandem mass spectrometry analyses indicated direct interactions of prohibitin and/or prohibiton with the (TGYCC)15 motif, which was confirmed by electrophoretic mobility shift assay and super-gel shift analysis with anti-prohibitin and anti-prohibiton antibodies. Using the chromatin immunopercipipation assay, we further demonstrated that prohibitin and prohibiton associated with the (TGYCC)15 motif in vivo regardless of the p53 status and apoptotic stress. We also found that prohibitin and prohibiton up-regulated PIG3 transcription independent of p53, although p53 obviously enhanced this process, and that the knock-down of prohibitin and prohibiton inhibited camptothecin-induced apoptosis. Taken together, our findings suggest that prohibitin and prohibiton contribute to PIG3-mediated apoptosis by binding to the PIG3 promoter (TGYCC)15 motif.
抑素诱导基因 3(PIG3)的启动子含有五核苷酸(TGYCC)n 的串联重复数可变,这是已知的 p53 结合位点。在这项研究中,我们研究了其他潜在的分子是否可以与这个 PIG3 启动子(TGYCC)n 基序结合。配体色谱结合液相色谱-串联质谱分析表明,阻遏蛋白和/或阻遏蛋白与(TGYCC)15 基序直接相互作用,这通过电泳迁移率变动分析和抗阻遏蛋白和抗阻遏蛋白抗体的超凝胶移位分析得到证实。使用染色质免疫沉淀分析,我们进一步证明了阻遏蛋白和阻遏蛋白与体内(TGYCC)15 基序相关,而与 p53 状态和凋亡应激无关。我们还发现,阻遏蛋白和阻遏蛋白独立于 p53 上调 PIG3 转录,尽管 p53 明显增强了这一过程,而阻遏蛋白和阻遏蛋白的敲低抑制了喜树碱诱导的细胞凋亡。总之,我们的研究结果表明,阻遏蛋白和阻遏蛋白通过与 PIG3 启动子(TGYCC)15 基序结合,促进 PIG3 介导的细胞凋亡。