Shan Bin, Xu Jin, Zhuo Ying, Morris Cindy A, Morris Gilbert F
Programs in Molecular and Cellular Biology and Lung Biology, Department of Pathology, Tulane Cancer Center and Tulane/Xavier Center for Bioenvironmental Research, New Orleans, Louisiana 70112, USA.
J Biol Chem. 2003 Nov 7;278(45):44009-17. doi: 10.1074/jbc.M302671200. Epub 2003 Aug 28.
A human fibroblast cell line with conditional p53 expression displayed a p53-dependent increase in both the protein and mRNA levels of proliferating cell nuclear antigen (PCNA) after exposure to ionizing radiation (IR). The combination of p53 induction and IR cooperated to activate a transiently expressed human PCNA promoter-reporter gene via a p53-responsive element. Chromatin immunoprecipitation assays with antibodies specific for p53 or p300/CREB-binding protein revealed specific p53-dependent enrichment of PCNA promoter sequences in immunoprecipitates of sheared chromatin prepared from irradiated cells. Maximal and specific association of acetylated histone H4 with the PCNA promoter also depended on p53 induction and exposure to IR. These data demonstrate p53 binding to a target site in the PCNA promoter, recruitment of p300/CREB-binding protein, and localized acetylation of histone H4 in an IR-dependent manner. These molecular events are likely to play a role in mediating activation of PCNA gene expression by p53 during the cellular response to DNA damage. The analyses indicate that the combination of p53 induction and IR activate the PCNA gene via mechanisms similar to that of p21/wild-type p53-activated factor but to a lesser extent. This differential regulation of PCNA and p21/wild-type p53-activated factor may establish the proper ratio of the two proteins to coordinate DNA repair with cell cycle arrest.
具有条件性p53表达的人成纤维细胞系在暴露于电离辐射(IR)后,增殖细胞核抗原(PCNA)的蛋白质和mRNA水平均呈现出p53依赖性增加。p53诱导与IR相结合,通过一个p53反应元件协同激活了瞬时表达的人PCNA启动子-报告基因。用针对p53或p300/CREB结合蛋白的特异性抗体进行的染色质免疫沉淀分析显示,在从受辐照细胞制备的剪切染色质的免疫沉淀中,PCNA启动子序列有特异性的p53依赖性富集。乙酰化组蛋白H4与PCNA启动子的最大且特异性结合也依赖于p53诱导和暴露于IR。这些数据表明p53与PCNA启动子中的一个靶位点结合,募集p300/CREB结合蛋白,并以IR依赖性方式使组蛋白H4发生局部乙酰化。这些分子事件可能在细胞对DNA损伤的反应过程中,介导p53对PCNA基因表达的激活中发挥作用。分析表明,p53诱导与IR的组合通过类似于p21/野生型p53激活因子的机制激活PCNA基因,但程度较小。PCNA和p21/野生型p53激活因子的这种差异调节可能会建立这两种蛋白质的适当比例,以协调DNA修复与细胞周期停滞。