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Ubiquitin E3 ligase UHRF1 regulates p53 ubiquitination and p53-dependent cell apoptosis in clear cell Renal Cell Carcinoma

机译:泛素E3连接酶UHRF1调节透明细胞肾细胞癌中的p53泛素化和p53依赖性细胞凋亡

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Ubiquitin-like with PHD and RING finger domain 1 (UHRF1) is a multi-domain ubiquitin E3 ligase that plays critical roles in regulation of DNA methylation and histone ubiquitination. In this study, we found UHRF1 is frequently overexpressed in human clear cell Renal Cell Carcinoma (ccRCC) tissues both at mRNA and protein levels. We showed that UHRF1 directly interacts with p53 both in vivo and in vitro. A new domain (PD) in UHRF1 was required for interaction with p53. We found that UHRF1 down-regulates p53 transactivation activity which was depends on the ubiquitin E3 ligase function. UHRF1 can promote non-degradative ubiquitination of p53, suppress p53 pathway activation and p53-dependent apoptosis in ccRCC cells. Together, our study suggests that UHRF1, which overexpressed ccRCC, may act as a p53 regulator, suppress p53 pathway activation and help ccRCC cells to escape from p53-dependent apoptosis. (C) 2015 Elsevier Inc. All rights reserved.
机译:具有PHD和RING指域1(UHRF1)的泛素样蛋白是一种多域泛素E3连接酶,在调节DNA甲基化和组蛋白泛素化中起关键作用。在这项研究中,我们发现UHRF1在人透明细胞肾细胞癌(ccRCC)组织中在mRNA和蛋白质水平上都经常过表达。我们表明,UHRF1在体内和体外都直接与p53相互作用。与p53相互作用需要UHRF1中的新域(PD)。我们发现UHRF1下调了p53反式激活活性,这取决于泛素E3连接酶功能。 UHRF1可以促进ccRCC细胞中p53的非降解泛素化,抑制p53途径活化和p53依赖性细胞凋亡。总之,我们的研究表明,过度表达ccRCC的UHRF1可能充当p53调节剂,抑制p53途径的活化并帮助ccRCC细胞摆脱p53依赖性细胞凋亡。 (C)2015 Elsevier Inc.保留所有权利。

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