Bates Gaynor J, Nicol Samantha M, Wilson Brian J, Jacobs Anne-Marie F, Bourdon Jean-Christophe, Wardrop Julie, Gregory David J, Lane David P, Perkins Neil D, Fuller-Pace Frances V
Department of Molecular & Cellular Pathology, University of Dundee, Ninewells Hospital & Medical School, Dundee, UK.
EMBO J. 2005 Feb 9;24(3):543-53. doi: 10.1038/sj.emboj.7600550. Epub 2005 Jan 20.
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-kappaB 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.
DEAD盒RNA解旋酶p68参与多种细胞过程,并已证明具有转录共激活因子功能。在此,我们表明p68与p53肿瘤抑制蛋白强烈协同作用,以刺激来自p53依赖性启动子的转录,并且内源性p68和p53从核提取物中共免疫沉淀。引人注目的是,RNA干扰抑制p68会抑制p53靶基因在DNA损伤反应中的表达以及p53依赖性凋亡,但不影响p53的稳定性或非p53反应性基因的表达。我们还通过染色质免疫沉淀表明,p68以p53依赖性方式被募集到p21启动子,这与促进转录起始的作用一致。有趣的是,p68敲低不会显著影响NF-κB激活,这表明p53转录活性的刺激不是由于一般的转录效应。本研究首次报道了RNA解旋酶参与p53反应,并突出了一种新机制,通过该机制p68可能作为肿瘤共抑制因子来调控p53转录活性。