Faculty of Medicine, University of Tsukuba, Tsukuba, Ibaraki, Japan.
PLoS One. 2013 Aug 13;8(8):e72496. doi: 10.1371/journal.pone.0072496. eCollection 2013.
The c-fos gene responds to extracellular stimuli and undergoes robust but transient transcriptional activation. Here we show that heterogeneous nuclear ribonucleoprotein R (hnRNP R) facilitates transcription reinitiation of the c-fos promoter in vitro in cooperation with Mediator. Consistently, hnRNP R interacts with the Scaffold components (Mediator, TBP, and TFIIH) as well as TFIIB, which recruits RNA polymerase II (Pol II) and TFIIF to Scaffold. The cooperative action of hnRNP R and Mediator is diminished by the cyclin-dependent kinase 8 (CDK8) module, which is comprised of CDK8, Cyclin C, MED12 and MED13 of the Mediator subunits. Interestingly, we find that the length of the G-free cassettes, and thereby their transcripts, influences the hnRNP R-mediated facilitation of reinitiation. Indeed, indicative of a possible role of the transcript in facilitating transcription reinitiation, the RNA transcript produced from the G-free cassette interacts with hnRNP R through its RNA recognition motifs (RRMs) and arginine-glycine-glycine (RGG) domain. Mutational analyses of hnRNP R indicate that facilitation of initiation and reinitiation requires distinct domains of hnRNP R. Knockdown of hnRNP R in mouse cells compromised rapid induction of the c-fos gene but did not affect transcription of constitutive genes. Together, these results suggest an important role for hnRNP R in regulating robust response of the c-fos gene.
c-fos 基因对细胞外刺激作出反应,并经历强烈但短暂的转录激活。在这里,我们表明异质核核糖核蛋白 R(hnRNP R)与 Mediator 合作,在体外促进 c-fos 启动子的转录重新起始。一致地,hnRNP R 与支架成分(Mediator、TBP 和 TFIIH)以及招募 RNA 聚合酶 II(Pol II)和 TFIIF 到支架的 TFIIB 相互作用。hnRNP R 和 Mediator 的协同作用被细胞周期蛋白依赖性激酶 8(CDK8)模块减弱,该模块由 CDK8、Cyclin C、Mediator 的 MED12 和 MED13 组成。有趣的是,我们发现 G-自由盒的长度,从而影响其转录物,影响 hnRNP R 介导的重新起始促进作用。事实上,作为促进转录重新起始的可能作用的指示,来自 G-自由盒的 RNA 转录本通过其 RNA 识别基序(RRMs)和精氨酸-甘氨酸-甘氨酸(RGG)结构域与 hnRNP R 相互作用。hnRNP R 的突变分析表明,起始和重新起始的促进需要 hnRNP R 的不同结构域。hnRNP R 在小鼠细胞中的敲低削弱了 c-fos 基因的快速诱导,但不影响组成型基因的转录。总之,这些结果表明 hnRNP R 在调节 c-fos 基因的强烈反应中起着重要作用。