Life Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, USA.
Nature. 2013 Mar 28;495(7442):481-6. doi: 10.1038/nature11991. Epub 2013 Feb 27.
Eukaryotic transcription initiation requires the assembly of general transcription factors into a pre-initiation complex that ensures the accurate loading of RNA polymerase II (Pol II) at the transcription start site. The molecular mechanism and function of this assembly have remained elusive due to lack of structural information. Here we have used an in vitro reconstituted system to study the stepwise assembly of human TBP, TFIIA, TFIIB, Pol II, TFIIF, TFIIE and TFIIH onto promoter DNA using cryo-electron microscopy. Our structural analyses provide pseudo-atomic models at various stages of transcription initiation that illuminate critical molecular interactions, including how TFIIF engages Pol II and promoter DNA to stabilize both the closed pre-initiation complex and the open-promoter complex, and to regulate start--initiation complexes, combined with the localization of the TFIIH helicases XPD and XPB, support a DNA translocation model of XPB and explain its essential role in promoter opening.
真核生物转录起始需要将一般转录因子组装成起始前复合物,以确保 RNA 聚合酶 II(Pol II)准确加载到转录起始位点。由于缺乏结构信息,这种组装的分子机制和功能仍然难以捉摸。在这里,我们使用体外重建的系统,使用冷冻电子显微镜研究人类 TBP、TFIIA、TFIIB、Pol II、TFIIF、TFIIE 和 TFIIH 如何逐步组装到启动子 DNA 上。我们的结构分析提供了转录起始各个阶段的拟原子模型,阐明了关键的分子相互作用,包括 TFIIF 如何与 Pol II 和启动子 DNA 结合,以稳定封闭的起始前复合物和开放启动子复合物,并调节起始-起始复合物,结合 XPD 和 XPB 这两种 TFIIH 解旋酶的定位,支持 XPB 的 DNA 易位模型,并解释其在启动子打开中的重要作用。