Song Lynda Li, Alimirah Fatouma, Panchanathan Ravichandran, Xin Hong, Choubey Divaker
Department of Environmental Health, University of Cincinnati, Cincinnati, Ohio 45267, USA.
Mol Cancer Res. 2008 Nov;6(11):1732-41. doi: 10.1158/1541-7786.MCR-08-0208. Epub 2008 Oct 30.
IFN-inducible IFI16 protein (encoded by IFI16 gene at 1q23.1) is the human member of the IFN-inducible structurally related p200 family proteins. Increased expression of the IFI16 protein, a positive modulator of p53-mediated transcription, in normal old human diploid fibroblasts (HDF) is associated with cellular senescence-mediated cell growth arrest. However, the underlying mechanisms that contribute to transcriptional activation of the IFI16 gene in old HDFs remain to be elucidated. Here, we reported that functional activation of p53 in normal young HDFs and p53-null Saos2 cell line resulted in transcriptional activation of the IFI16 gene. We identified a potential p53 DNA-binding site (indicated as IFI16-p53-BS) in the 5'-regulatory region of the IFI16 gene. Importantly, p53 bound to IFI16-p53-BS in a sequence-specific manner in gel-mobility shift assays. Furthermore, p53 associated with the 5'-regulatory region of the IFI16 gene in chromatin immunoprecipitation assays. Interestingly, p53 associated with the regulatory region of the IFI16 gene only on treatment of cells with DNA-damaging agents or in the old, but not in the young, HDFs. Importantly, our promoter-reporter assays, which were coupled with site-directed mutagenesis of IFI16-p53-BS, showed that p53 activates transcription of the IFI16 gene in HDFs through the p53 DNA-binding site. Together, our observations provide support for the idea that up-regulation of IFI16 expression by p53 and functional interactions between IFI16 protein and p53 contribute to cellular senescence.
干扰素诱导的IFI16蛋白(由位于1q23.1的IFI16基因编码)是干扰素诱导的结构相关p200家族蛋白的人类成员。IFI16蛋白是p53介导转录的正向调节因子,在正常老年人类二倍体成纤维细胞(HDF)中其表达增加与细胞衰老介导的细胞生长停滞相关。然而,老年HDF中导致IFI16基因转录激活的潜在机制仍有待阐明。在此,我们报道正常年轻HDF和p53基因缺失的Saos2细胞系中p53的功能激活导致了IFI16基因的转录激活。我们在IFI16基因的5'调控区域鉴定出一个潜在的p53 DNA结合位点(表示为IFI16-p53-BS)。重要的是,在凝胶迁移率变动分析中,p53以序列特异性方式结合到IFI16-p53-BS。此外,在染色质免疫沉淀分析中,p53与IFI16基因的5'调控区域相关联。有趣的是,仅在用DNA损伤剂处理细胞时或在老年HDF中,而非年轻HDF中,p53与IFI16基因的调控区域相关联。重要的是,我们结合IFI16-p53-BS定点诱变的启动子报告基因分析表明,p53通过p53 DNA结合位点激活HDF中IFI16基因的转录。总之,我们的观察结果支持以下观点:p53上调IFI16表达以及IFI16蛋白与p53之间的功能相互作用促成细胞衰老。