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首页> 外文期刊>Oncogene >A novel HECT-type E3 ubiquitin protein ligase NEDL1 enhances the p53-mediated apoptotic cell death in its catalytic activity-independent manner
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A novel HECT-type E3 ubiquitin protein ligase NEDL1 enhances the p53-mediated apoptotic cell death in its catalytic activity-independent manner

机译:一种新型的HECT型E3泛素蛋白连接酶NEDL1以其催化活性非依赖性方式增强p53介导的凋亡细胞死亡

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NEDL1 (NEDD4-like ubiquitin protein ligase-1) is a newly identified HECT-type E3 ubiquitin protein ligase highly expressed in favorable neuroblastomas as compared with unfavorable ones. In this study, we found that NEDL1 cooperates with p53 to induce apoptosis. During cisplatin (CDDP)-mediated apoptosis in neuroblastoma SH-SY5Y cells, p53 was induced to accumulate in association with an increase in expression levels of NEDL1. Enforced expression of NEDL1 resulted in a decrease in number of G418-resistant colonies in SH-SY5Y and U2OS cells bearing wild-type p53, whereas NEDL1 had undetectable effect on p53-deficient H1299 and SAOS-2 cells. Similarly, enforced expression of NEDL1 increased number of U2OS cells with sub-G1 DNA content. Co-immunoprecipitation and in vitro binding assays revealed that NEDL1 binds to the COOH-terminal region of p53. Luciferase reporter assay showed that NEDL1 has an ability to enhance the transcriptional activity of p53. Small interfering RNA-mediated knockdown of the endogenous NEDL1 conferred the resistance of U2OS cells to adriamycin. It is noteworthy that NEDL1 enhanced pro-apoptotic activity of p53 in its catalytic activity-independent manner. Taken together, our present findings suggest that functional interaction of NEDL1 with p53 might contribute to the induction of apoptosis in cancerous cells bearing wild-type p53.
机译:NEDL1(NEDD4样泛素蛋白连接酶-1)是一种新近鉴定的HECT型E3泛素蛋白连接酶,在不良神经母细胞瘤中高表达。在这项研究中,我们发现NEDL1与p53协同诱导凋亡。在顺铂(CDDP)介导的神经母细胞瘤SH-SY5Y细胞凋亡中,p53被诱导积累与NEDL1表达水平的增加有关。 NEDL1的强制表达导致携带野生型p53的SH-SY5Y和U2OS细胞中G418耐药菌落的数量减少,而NEDL1对p53缺失的H1299和SAOS-2细胞却无法检测到。同样,NEDL1的强制表达增加了具有亚G1 DNA含量的U2OS细胞的数量。免疫共沉淀和体外结合试验表明NEDL1与p53的COOH末端区域结合。萤光素酶报告基因检测表明NEDL1具有增强p53转录活性的能力。 RNA介导的内源性NEDL1的小干扰敲除赋予U2OS细胞对阿霉素的抗性。值得注意的是,NEDL1以不依赖催化活性的方式增强了p53的促凋亡活性。综上所述,我们目前的发现表明NEDL1与p53的功能相互作用可能有助于诱导带有野生型p53的癌细胞凋亡。

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