Nakadai Tomoyoshi, Fukuda Aya, Shimada Miho, Nishimura Ken, Hisatake Koji
From the Department of Molecular Biology, Faculty of Medicine, Saitama Medical University, 38 Morohongo, Moroyama, Iruma-gun, Saitama 350-0495, Japan and.
Department of Biochemistry, Faculty of Medicine, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki 305-8575, Japan.
J Biol Chem. 2015 Oct 30;290(44):26832-45. doi: 10.1074/jbc.M115.688317. Epub 2015 Sep 17.
The c-fos gene is rapidly induced to high levels by various extracellular stimuli. We used a defined in vitro transcription system that utilizes the c-fos promoter to purify a coactivator activity in an unbiased manner. We report here that NF45-NF90 and NF45-NF110, which possess archetypical double-stranded RNA binding motifs, have a direct function as transcriptional coactivators. The transcriptional activities of the nuclear factor (NF) complexes (NF45-NF90 and NF45-NF110) are mediated by both the upstream enhancer and core promoter regions of the c-fos gene and do not require their double-stranded RNA binding activities. The NF complexes cooperate with general coactivators, PC4 and Mediator, to elicit a high level of transcription and display multiple interactions with activators and the components of the general transcriptional machinery. Knockdown of the endogenous NF90/NF110 in mouse cells shows an important role for the NF complexes in inducing c-fos transcription. Chromatin immunoprecipitation assays demonstrate that the NF complexes occupy the c-fos enhancer/promoter region before and after serum induction and that their occupancies within the coding region of the c-fos gene increase in parallel to that of RNAPII upon serum induction. In light of their dynamic occupancy on the c-fos gene as well as direct functions in both transcription and posttranscriptional processes, the NF complexes appear to serve as multifunctional coactivators that coordinate different steps of gene expression to facilitate rapid response of inducible genes.
c-fos基因可被多种细胞外刺激迅速诱导至高水平。我们使用了一种特定的体外转录系统,该系统利用c-fos启动子以无偏差的方式纯化一种共激活因子活性。我们在此报告,具有典型双链RNA结合基序的NF45-NF90和NF45-NF110具有作为转录共激活因子的直接功能。核因子(NF)复合物(NF45-NF90和NF45-NF110)的转录活性由c-fos基因的上游增强子和核心启动子区域介导,并且不需要它们的双链RNA结合活性。NF复合物与一般共激活因子PC4和中介体协同作用,以引发高水平的转录,并与激活因子和一般转录机制的组分表现出多种相互作用。在小鼠细胞中敲低内源性NF90/NF110表明NF复合物在诱导c-fos转录中起重要作用。染色质免疫沉淀分析表明,NF复合物在血清诱导前后占据c-fos增强子/启动子区域,并且它们在c-fos基因编码区域内的占据率在血清诱导后与RNA聚合酶II的占据率平行增加。鉴于它们在c-fos基因上的动态占据以及在转录和转录后过程中的直接功能,NF复合物似乎作为多功能共激活因子,协调基因表达的不同步骤以促进可诱导基因的快速反应。