State Key Laboratory of Cell Biology, Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, China.
Mol Cell. 2012 Feb 24;45(4):459-69. doi: 10.1016/j.molcel.2011.12.022. Epub 2012 Jan 19.
Mediator complex is an integrative hub for transcriptional regulation. Here we show that Mediator regulates alternative mRNA processing via its MED23 subunit. Combining tandem affinity purification and mass spectrometry, we identified a number of mRNA processing factors that bind to a soluble recombinant Mediator subunit, MED23, but not to several other Mediator components. One of these factors, hnRNP L, specifically interacts with MED23 in vitro and in vivo. Consistently, Mediator partially colocalizes with hnRNP L and the splicing machinery in the cell. Functionally, MED23 regulates a subset of hnRNP L-targeted alternative splicing (AS) and alternative cleavage and polyadenylation (APA) events, as shown by minigene reporters and exon array analysis. ChIP-seq analysis revealed that MED23 can regulate hnRNP L occupancy at their coregulated genes. Taken together, these results demonstrate a crosstalk between Mediator and the splicing machinery, providing a molecular basis for coupling mRNA processing to transcription.
中介复合物是转录调控的综合枢纽。在这里,我们表明中介通过其 MED23 亚基调节选择性 mRNA 加工。通过串联亲和纯化和质谱分析,我们鉴定出许多与可溶性重组中介亚基 MED23 结合但不与其他几种中介成分结合的 mRNA 加工因子。这些因子之一,hnRNP L,在体外和体内特异性与 MED23 相互作用。一致地,中介复合物部分与 hnRNP L 和剪接机制在细胞中共定位。功能上,MED23 调节 hnRNP L 靶向的选择性剪接 (AS) 和选择性剪接和多聚腺苷酸化 (APA) 事件的子集,如通过迷你基因报告基因和外显子阵列分析所示。ChIP-seq 分析显示,MED23 可以调节 hnRNP L 在其共调控基因上的占有率。总之,这些结果表明中介复合物和剪接机制之间存在串扰,为将 mRNA 加工与转录偶联提供了分子基础。