首页> 外文期刊>Molecular cancer research: MCR >Expression of an IFN-inducible cellular senescence gene, IFI16, is up-regulated by p53.
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Expression of an IFN-inducible cellular senescence gene, IFI16, is up-regulated by p53.

机译:p53上调了IFN诱导的细胞衰老基因IFI16的表达。

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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.
机译:IFN诱导型IFI16蛋白(在1q23.1由IFI16基因编码)是IFN诱导型结构相关p200家族蛋白的人类成员。在正常的老年人二倍体成纤维细胞(HDF)中,IFI16蛋白(p53介导的转录的正调节剂)表达的增加与细胞衰老介导的细胞生长停滞有关。但是,有助于阐明旧HDF中IFI16基因转录激活的潜在机制尚待阐明。在这里,我们报道正常的年轻HDF和p53无效的Saos2细胞系中p53的功能激活导致IFI16基因的转录激活。我们在IFI16基因的5'调控区中发现了一个潜在的p53 DNA结合位点(表示为IFI16-p53-BS)。重要的是,在凝胶迁移率测定中,p53以序列特异性的方式与IFI16-p53-BS结合。此外,在染色质免疫沉淀试验中,p53与IFI16基因的5'调节区相关。有趣的是,p53仅在用DNA损伤剂处理细胞时才与IFI16基因的调节区相关联,或者在老年人中,而在年轻的HDFs中则不相关。重要的是,我们的启动子-报告基因检测与IFI16-p53-BS的定点诱变相结合,显示p53通过p53 DNA结合位点激活HDF中IFI16基因的转录。总之,我们的观察结果为以下观点提供了支持:p53对IFI16表达的上调以及IFI16蛋白与p53之间的功能性相互作用有助于细胞衰老。

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