Cramer P
Gene Center Munich, Department of Chemistry and Biochemistry, Ludwig-Maximilians-Universität München, Feodor-Lynen-Strasse 25, 81377 Munich, Germany.
Biochem Soc Trans. 2006 Dec;34(Pt 6):1058-61. doi: 10.1042/BST0341058.
Here, I review three new structural studies from our laboratory. First, the crystal structure of RNA polymerase (Pol) II in complex with an RNA inhibitor revealed that this RNA blocks transcription initiation by preventing DNA loading into the active-centre cleft. Secondly, the structure of the SRI (Set2 Rpb1-interacting) domain of the histone methyltransferase Set2 revealed a novel fold for specific interaction with the doubly phosphorylated CTD (C-terminal repeat domain) of Pol II. Finally, we obtained the first structural information on Pol III, in the form of an 11-subunit model obtained by combining a homology model of the nine-subunit core enzyme with a new X-ray structure of the subcomplex C17/25.
在此,我回顾了我们实验室的三项新的结构研究。首先,RNA聚合酶(Pol)II与一种RNA抑制剂复合物的晶体结构表明,这种RNA通过阻止DNA进入活性中心裂隙来阻断转录起始。其次,组蛋白甲基转移酶Set2的SRI(Set2与Rpb1相互作用)结构域的结构揭示了一种与Pol II的双磷酸化CTD(C末端重复结构域)特异性相互作用的新折叠。最后,我们以一个11亚基模型的形式获得了关于Pol III的首个结构信息,该模型是通过将九亚基核心酶的同源模型与亚复合物C17/25的新X射线结构相结合得到的。