Department of Biological Sciences, Wayne State University, Detroit, Michigan 48202, USA.
J Biol Chem. 2013 Apr 19;288(16):11384-94. doi: 10.1074/jbc.M112.446773. Epub 2013 Mar 8.
We have earlier demonstrated the involvement of Mediator subunit Srb5/Med18 in the termination of transcription for a subset of genes in yeast. Srb5/Med18 could affect termination either indirectly by modulating CTD-Ser(2) phosphorylation near the 3' end of a gene or directly by physically interacting with the cleavage and polyadenylation factor or cleavage factor 1 (CF1) complex and facilitating their recruitment to the terminator region. Here, we show that the CTD-Ser(2) phosphorylation pattern on Srb5/Med18-dependent genes remains unchanged in the absence of Srb5 in cells. Coimmunoprecipitation analysis revealed the physical interaction of Srb5/Med18 with the CF1 complex. No such interaction of Srb5/Med18 with the cleavage and polyadenylation factor complex, however, could be detected. The Srb5/Med18-CF1 interaction was not observed in the looping defective sua7-1 strain. Srb5/Med18 cross-linking to the 3' end of genes was also abolished in the sua7-1 strain. Chromosome conformation capture analysis revealed that the looped architecture of Srb5/Med18-dependent genes was abrogated in srb5(-) cells. Furthermore, Srb5-dependent termination of transcription was compromised in the looping defective sua7-1 cells. The overall conclusion of these results is that gene looping plays a crucial role in Srb5/Med18 facilitated termination of transcription, and the looped gene architecture may have a general role in termination of transcription in budding yeast.
我们之前已经证明 Mediator 亚基 Srb5/Med18 参与了酵母中一组基因转录的终止。Srb5/Med18 可以通过调节 CTD-Ser(2)在基因 3' 末端附近的磷酸化来间接影响终止,或者直接与切割和多聚腺苷酸化因子或切割因子 1 (CF1) 复合物相互作用,并促进它们在终止子区域的募集。在这里,我们表明,在没有 Srb5 的情况下,Srb5/Med18 依赖性基因的 CTD-Ser(2)磷酸化模式在细胞中保持不变。共免疫沉淀分析显示 Srb5/Med18 与 CF1 复合物的物理相互作用。然而,未检测到 Srb5/Med18 与切割和多聚腺苷酸化因子复合物的这种相互作用。在环缺失 sua7-1 菌株中未观察到 Srb5/Med18 与 CF1 相互作用。Srb5/Med18 与基因 3' 末端的交联也在 sua7-1 菌株中被废除。染色体构象捕获分析显示,Srb5/Med18 依赖性基因的环化结构在 srb5(-) 细胞中被破坏。此外,转录的 Srb5 依赖性终止在环缺失缺陷 sua7-1 细胞中受到损害。这些结果的总体结论是,基因环化在 Srb5/Med18 促进的转录终止中起着至关重要的作用,并且环化的基因结构可能在芽殖酵母的转录终止中具有普遍作用。