Lee Jookyung, Borukhov Sergei
Department of Cell Biology, Rowan University School of Osteopathic Medicine Stratford, NJ, USA.
Front Mol Biosci. 2016 Nov 9;3:73. doi: 10.3389/fmolb.2016.00073. eCollection 2016.
DNA-dependent multisubunit RNA polymerase (RNAP) is the key enzyme of gene expression and a target of regulation in all kingdoms of life. It is a complex multifunctional molecular machine which, unlike other DNA-binding proteins, engages in extensive and dynamic interactions (both specific and nonspecific) with DNA, and maintains them over a distance. These interactions are controlled by DNA sequences, DNA topology, and a host of regulatory factors. Here, we summarize key recent structural and biochemical studies that elucidate the fine details of RNAP-DNA interactions during initiation. The findings of these studies help unravel the molecular mechanisms of promoter recognition and open complex formation, initiation of transcript synthesis and promoter escape. We also discuss most current advances in the studies of drugs that specifically target RNAP-DNA interactions during transcription initiation and elongation.
依赖DNA的多亚基RNA聚合酶(RNAP)是基因表达的关键酶,也是所有生命王国中调控的靶点。它是一个复杂的多功能分子机器,与其他DNA结合蛋白不同,它与DNA进行广泛而动态的相互作用(包括特异性和非特异性),并在一定距离内维持这些相互作用。这些相互作用受DNA序列、DNA拓扑结构和许多调控因子的控制。在这里,我们总结了最近的关键结构和生化研究,这些研究阐明了起始过程中RNAP-DNA相互作用的精细细节。这些研究结果有助于揭示启动子识别和开放复合物形成、转录本合成起始和启动子逃逸的分子机制。我们还讨论了在转录起始和延伸过程中特异性靶向RNAP-DNA相互作用的药物研究的最新进展。