首页> 美国卫生研究院文献>The Journal of Biological Chemistry >Cyclin-dependent Kinase 8 Module Expression Profiling Reveals Requirement of Mediator Subunits 12 and 13 for Transcription of Serpent-dependent Innate Immunity Genes in Drosophila
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Cyclin-dependent Kinase 8 Module Expression Profiling Reveals Requirement of Mediator Subunits 12 and 13 for Transcription of Serpent-dependent Innate Immunity Genes in Drosophila

机译:细胞周期蛋白依赖性激酶8模块表达谱揭示果蝇蛇依赖天然免疫基因转录的调解员亚基12和13的要求。

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摘要

The Cdk8 (cyclin-dependent kinase 8) module of Mediator integrates regulatory cues from transcription factors to RNA polymerase II. It consists of four subunits where Med12 and Med13 link Cdk8 and cyclin C (CycC) to core Mediator. Here we have investigated the contributions of the Cdk8 module subunits to transcriptional regulation using RNA interference in Drosophila cells. Genome-wide expression profiling demonstrated separation of Cdk8-CycC and Med12-Med13 profiles. However, transcriptional regulation by Cdk8-CycC was dependent on Med12-Med13. This observation also revealed that Cdk8-CycC and Med12-Med13 often have opposite transcriptional effects. Interestingly, Med12 and Med13 profiles overlapped significantly with that of the GATA factor Serpent. Accordingly, mutational analyses indicated that GATA sites are required for Med12-Med13 regulation of Serpent-dependent genes. Med12 and Med13 were also found to be required for Serpent-activated innate immunity genes in defense to bacterial infection. The results reveal a novel role for the Cdk8 module in Serpent-dependent transcription and innate immunity.
机译:Mediator的Cdk8(细胞周期蛋白依赖性激酶8)模块整合了从转录因子到RNA聚合酶II的调控信号。它由四个亚基组成,其中Med12和Med13将Cdk8和细胞周期蛋白C(CycC)连接到核心介体。在这里,我们研究了果蝇细胞中使用RNA干扰的Cdk8模块亚基对转录调控的贡献。全基因组表达谱表明Cdk8-CycC和Med12-Med13配置文件的分离。但是,Cdk8-CycC的转录调控取决于Med12-Med13。该观察结果还表明,Cdk8-CycC和Med12-Med13通常具有相反的转录作用。有趣的是,Med12和Med13谱与GATA因子蛇的谱显着重叠。因此,突变分析表明,Gata位点是蛇依赖基因的Med12-Med13调控所必需的。还发现Med12和Med13是蛇激活的先天免疫基因在防御细菌感染中所必需的。结果揭示了Cdk8模块在蛇依赖性转录和先天免疫中的新作用。

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