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The DEAD box protein p68: a novel transcriptional coactivator of the p53 tumour suppressor

机译:DEAD box蛋白p68:p53肿瘤抑制因子的新型转录共激活因子

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摘要

The DEAD box RNA helicase, p68, has been implicated in various cellular processes and has been shown to possess transcriptional coactivator function. Here, we show that p68 potently synergises with the p53 tumour suppressor protein to stimulate transcription from p53-dependent promoters and that endogenous p68 and p53 co-immunoprecipitate from nuclear extracts. Strikingly, RNAi suppression of p68 inhibits p53 target gene expression in response to DNA damage, as well as p53-dependent apoptosis, but does not influence p53 stabilisation or expression of non-p53-responsive genes. We also show, by chromatin immunoprecipitation, that p68 is recruited to the p21 promoter in a p53-dependent manner, consistent with a role in promoting transcriptional initiation. Interestingly, p68 knock-down does not significantly affect NF-κB activation, suggesting that the stimulation of p53 transcriptional activity is not due to a general transcription effect. This study represents the first report of the involvement of an RNA helicase in the p53 response, and highlights a novel mechanism by which p68 may act as a tumour cosuppressor in governing p53 transcriptional activity.
机译:DEAD盒RNA解旋酶p68与多种细胞过程有关,并显示具有转录共激活功能。在这里,我们显示p68与p53抑癌蛋白有效协同作用,以刺激p53依赖型启动子的转录,内源性p68和p53从核提取物中共免疫沉淀。令人惊讶的是,RNAi对p68的抑制作用可抑制p53靶基因的表达,以响应DNA损伤以及p53依赖性凋亡,但不影响p53稳定或非p53响应基因的表达。通过染色质免疫沉淀,我们还显示p68以p53依赖性方式被募集到p21启动子,与促进转录起始的作用一致。有趣的是,p68敲低并不显着影响NF-κB的激活,这表明对p53转录活性的刺激不是由于一般的转录作用。这项研究代表了RNA解旋酶参与p53反应的第一个报道,并着重介绍了一种新的机制,通过该机制,p68可以在控制p53转录活性中充当肿瘤抑制因子。

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