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Differential regulation of human YY1 and caspase 7 promoters by prohibitin through E2F1 and p53 binding sites

机译:禁止素通过E2F1和p53结合位点对人YY1和caspase 7启动子的差异调节

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pProhibitin is a 30 kDa growth suppressive protein that has pleiotropic functions in the cell. Although prohibitin has been demonstrated to have potent transcriptional regulatory functions, it has also been proposed to facilitate protein folding in the mitochondria and promote cell migration in association with Raf-1. Our previous studies have shown that prohibitin physically interacts with the marked-box domain of E2F family members and represses their transcriptional activity; in contrast, prohibitin could bind to and enhance the transcriptional activity of p53. Here, we show that promoters of human iYY1/i (Yin and Yang 1) as well as icaspase 7/i genes are modulated by prohibitin. iYY1/i promoter activity was reduced upon overexpression of prohibitin, while it was enhanced when prohibitin was depleted by small interfering RNA techniques. The repressive effects of prohibitin on the iYY1/i promoter were mediated through E2F binding sites, as seen by mutational analysis and chromatin immunoprecipitation assays. Further, depletion of E2F1 prevented prohibitin from repressing the iYY1/i promoter. In contrast with iYY1/i, prohibitin overexpression led to enhanced levels of icaspase 7/i, whereas depletion of prohibitin reduced it. Interestingly, the icaspase 7/i promoter was found to have p53-binding sites and prohibitin activated this promoter through p53. These studies show that prohibitin can have diverse effects on the expression of different genes and the activity of various cellular promoters is affected by prohibitin. Further, it appears very likely that prohibitin carries out many of its cellular functions by affecting the transcription of different genes./p
机译:> Prohibitin是一种30 kDa的生长抑制蛋白,在细胞中具有多效性功能。尽管已证明禁止素具有强大的转录调节功能,但也有人提出它可以促进蛋白质在线粒体中折叠并促进与Raf-1结合的细胞迁移。我们以前的研究表明,禁止素与E2F家族成员的标记框结构域发生物理相互作用,并抑制其转录活性。相反,禁止素可与p53结合并增强其转录活性。在这里,我们显示了人类 YY1 (Yin和Yang 1)的启动子以及 caspase 7 基因的启动子是由禁止素调节的。 YY1 启动子的活性在禁止素过度表达时降低,而在通过小干扰RNA技术耗尽禁止素后增强。突变分析和染色质免疫沉淀分析表明,禁止素通过E2F结合位点介导了抑制素对 YY1 启动子的抑制作用。此外,E2F1的消耗阻止了禁止素抑制 YY1 启动子。与 YY1 相比,禁止素的过表达导致 caspase 7 的水平升高,而禁止素的消耗则降低了它。有趣的是,发现 caspase 7 启动子具有p53结合位点,而抑制素则通过p53激活了该启动子。这些研究表明,禁止素可以对不同基因的表达产生多种影响,并且各种细胞启动子的活性都受到禁止素的影响。此外,禁止素很可能会通过影响不同基因的转录来发挥其许多细胞功能。

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