Department of Molecular Biology, Max Planck Institute for Biophysical Chemistry, 37077 Göttingen, Germany; email:
Current affiliation: Institute of Biochemistry, Genetics and Microbiology, University of Regensburg, 93053 Regensburg, Germany; email:
Annu Rev Biophys. 2018 May 20;47:425-446. doi: 10.1146/annurev-biophys-070317-033058.
RNA polymerases I and II (Pol I and Pol II) are the eukaryotic enzymes that catalyze DNA-dependent synthesis of ribosomal RNA and messenger RNA, respectively. Recent work shows that the transcribing forms of both enzymes are similar and the fundamental mechanisms of RNA chain elongation are conserved. However, the mechanisms of transcription initiation and its regulation differ between Pol I and Pol II. Recent structural studies of Pol I complexes with transcription initiation factors provided insights into how the polymerase recognizes its specific promoter DNA, how it may open DNA, and how initiation may be regulated. Comparison with the well-studied Pol II initiation system reveals a distinct architecture of the initiation complex and visualizes promoter- and gene-class-specific aspects of transcription initiation. On the basis of new structural studies, we derive a model of the Pol I transcription cycle and provide a molecular movie of Pol I transcription that can be used for teaching.
RNA 聚合酶 I 和 II(Pol I 和 Pol II)是分别催化核糖体 RNA 和信使 RNA 依赖于 DNA 的合成的真核酶。最近的研究表明,这两种酶的转录形式相似,并且 RNA 链延伸的基本机制是保守的。然而,Pol I 和 Pol II 之间的转录起始机制和调控机制不同。最近对 Pol I 与转录起始因子复合物的结构研究提供了有关聚合酶如何识别其特定启动子 DNA、如何打开 DNA 以及如何进行调控的见解。与研究充分的 Pol II 起始系统的比较揭示了起始复合物的独特结构,并可视化了转录起始的启动子和基因类别特异性方面。基于新的结构研究,我们得出了 Pol I 转录循环的模型,并提供了 Pol I 转录的分子电影,可用于教学。