Nogales Eva, Louder Robert K, He Yuan
Molecular and Cell Biology Department and QB3 Institute, University of California, Berkeley, California 94720-3220.
Howard Hughes Medical Institute, Berkeley, California 94720-3220.
Annu Rev Biophys. 2017 May 22;46:59-83. doi: 10.1146/annurev-biophys-070816-033751.
Eukaryotic gene transcription requires the assembly at the promoter of a large preinitiation complex (PIC) that includes RNA polymerase II (Pol II) and the general transcription factors TFIID, TFIIA, TFIIB, TFIIF, TFIIE, and TFIIH. The size and complexity of Pol II, TFIID, and TFIIH have precluded their reconstitution from heterologous systems, and purification relies on scarce endogenous sources. Together with their conformational flexibility and the transient nature of their interactions, these limitations had precluded structural characterization of the PIC. In the last few years, however, progress in cryo-electron microscopy (cryo-EM) has made possible the visualization, at increasingly better resolution, of large PIC assemblies in different functional states. These structures can now be interpreted in near-atomic detail and provide an exciting structural framework for past and future functional studies, giving us unique mechanistic insight into the complex process of transcription initiation.
真核基因转录需要在启动子处组装一个大型的预起始复合物(PIC),该复合物包括RNA聚合酶II(Pol II)以及通用转录因子TFIID、TFIIA、TFIIB、TFIIF、TFIIE和TFIIH。Pol II、TFIID和TFIIH的大小和复杂性使得它们无法从异源系统中重组,纯化依赖于稀缺的内源性来源。再加上它们构象的灵活性及其相互作用的短暂性,这些限制使得PIC的结构表征难以实现。然而,在过去几年中,冷冻电子显微镜(cryo-EM)技术的进步使得以越来越高的分辨率可视化处于不同功能状态的大型PIC组装体成为可能。现在可以近乎原子级的细节来解读这些结构,为过去和未来的功能研究提供了一个令人兴奋的结构框架,让我们对转录起始的复杂过程有了独特的机制性见解。