Schneider Maren, Hellerschmied Doris, Schubert Tobias, Amlacher Stefan, Vinayachandran Vinesh, Reja Rohit, Pugh B Franklin, Clausen Tim, Köhler Alwin
Max F. Perutz Laboratories, Medical University of Vienna, Vienna Biocenter Campus (VBC), Dr. Bohr-Gasse 9/3, 1030 Vienna, Austria.
Research Institute of Molecular Pathology, Dr. Bohr-Gasse 7, 1030 Vienna, Austria.
Cell. 2015 Aug 27;162(5):1016-28. doi: 10.1016/j.cell.2015.07.059.
Nuclear pore complexes (NPCs) influence gene expression besides their established function in nuclear transport. The TREX-2 complex localizes to the NPC basket and affects gene-NPC interactions, transcription, and mRNA export. How TREX-2 regulates the gene expression machinery is unknown. Here, we show that TREX-2 interacts with the Mediator complex, an essential regulator of RNA Polymerase (Pol) II. Structural and biochemical studies identify a conserved region on TREX-2, which directly binds the Mediator Med31/Med7N submodule. TREX-2 regulates assembly of Mediator with the Cdk8 kinase and is required for recruitment and site-specific phosphorylation of Pol II. Transcriptome and phenotypic profiling confirm that TREX-2 and Med31 are functionally interdependent at specific genes. TREX-2 additionally uses its Mediator-interacting surface to regulate mRNA export suggesting a mechanism for coupling transcription initiation and early steps of mRNA processing. Our data provide mechanistic insight into how an NPC-associated adaptor complex accesses the core transcription machinery.
核孔复合体(NPCs)除了在核运输中具有既定功能外,还影响基因表达。TREX - 2复合体定位于NPC篮,并影响基因与NPC的相互作用、转录和mRNA输出。TREX - 2如何调节基因表达机制尚不清楚。在这里,我们表明TREX - 2与中介体复合体相互作用,中介体复合体是RNA聚合酶(Pol)II的重要调节因子。结构和生化研究确定了TREX - 2上的一个保守区域,该区域直接结合中介体的Med31/Med7N亚模块。TREX - 2调节中介体与Cdk8激酶的组装,并且是Pol II募集和位点特异性磷酸化所必需的。转录组和表型分析证实,TREX - 2和Med31在特定基因上功能相互依赖。TREX - 2还利用其与中介体相互作用的表面来调节mRNA输出,这提示了一种耦合转录起始和mRNA加工早期步骤的机制。我们的数据为NPC相关衔接复合体如何进入核心转录机制提供了机制性见解。