Martinez-Rucobo Fuensanta W, Cramer Patrick
Department of Biochemistry, Ludwig-Maximilians-Universität München, Munich, Germany.
Biochim Biophys Acta. 2013 Jan;1829(1):9-19. doi: 10.1016/j.bbagrm.2012.09.002. Epub 2012 Sep 13.
For transcription elongation, all cellular RNA polymerases form a stable elongation complex (EC) with the DNA template and the RNA transcript. Since the millennium, a wealth of structural information and complementary functional studies provided a detailed three-dimensional picture of the EC and many of its functional states. Here we summarize these studies that elucidated EC structure and maintenance, nucleotide selection and addition, translocation, elongation inhibition, pausing and proofreading, backtracking, arrest and reactivation, processivity, DNA lesion-induced stalling, lesion bypass, and transcriptional mutagenesis. In the future, additional structural and functional studies of elongation factors that control the EC and their possible allosteric modes of action should result in a more complete understanding of the dynamic molecular mechanisms underlying transcription elongation. This article is part of a Special Issue entitled: RNA polymerase II Transcript Elongation.
对于转录延伸,所有细胞RNA聚合酶都会与DNA模板和RNA转录本形成稳定的延伸复合物(EC)。自千禧年以来,大量的结构信息和互补的功能研究提供了延伸复合物及其许多功能状态的详细三维图景。在此,我们总结了这些阐明延伸复合物结构与维持、核苷酸选择与添加、转位、延伸抑制、暂停与校对、回溯、停滞与重新激活、持续合成能力、DNA损伤诱导的停滞、损伤绕过和转录诱变的研究。未来,对控制延伸复合物的延伸因子及其可能的变构作用模式进行更多的结构和功能研究,将有助于更全面地理解转录延伸背后的动态分子机制。本文是名为“RNA聚合酶II转录延伸”的特刊的一部分。