Structural study of direct associations between cellular RNA polymerase and regulatory factors during the transcription cycle

转录周期中细胞 RNA 聚合酶与调节因子之间直接关联的结构研究

• 批准号: 10120099
• 负责人: Katsuhiko Murakami
• 金额: $ 8.22万
• 依托单位: PENNSYLVANIA STATE UNIVERSITY, THE
• 依托单位国家: 美国
• 财政年份: 2019
• 资助国家: 美国
• 起止时间: 2019-07-01 至 2024-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10120099
• 关键词: Archaea; Archaeal RNA; Bacteria; Bacterial RNA; Biochemical; Cell physiology; Cells; Cellular biology; Complex; Coupled; Cryoelectron Microscopy; Crystallization; DNA Repair; DNA-Directed RNA Polymerase; Development; Disease; Enzymes; Escherichia coli; Gene Expression; Genetic Transcription; Goals; Holoenzymes; Human; Lead; Life; Ligands; Macromolecular Complexes; Mainstreaming; Maintenance; Methods; Molecular Structure; Motor; Nature; Pathway interactions; Play; Polymerase; Research; Resolution; Role; Structure; Transcription Elongation; Transcription Initiation; Transcription Process; Transcriptional Regulation; X-Ray Crystallography; drug discovery; improved; insight; macromolecular assembly; prevent; promoter; response; structural biology; termination factor; transcription termination

Project Summary The long-term goal of our research is to understand transcription mechanisms of cellular RNA polymerase. Our research has made major contributions to provide structures of RNA polymerase at the different stage of transcription cycle. During the next five years, we will continue to study the transcription machinery in bacteria and archaea to provide insights of the fundamental mechanism of transcription, which is conserved from bacteria to human. Over the last 20 years, X-ray crystallography has been playing a major role in the structural biology of RNA polymerase and revealed many important structures. RNA polymerases at evident stages in the mainstream of the transcription cycle are often referred to RNA polymerase core enzyme, holoenzymes, open complex with a strong promoter, transcription initiation and elongation complexes. These structures have been well characterized due to their stable natures. A challenge in the structural biology of cellular RNA polymerase is to visualize transient interactions of RNA polymerase with other regulatory factors and ligands that occur in between each evident stage in the mainstream or at the branched pathways from the mainstream of transcription cycle. Due to their elusive natures, crystallization of such macromolecular assemblies has been a bottleneck and thus limited the approach by X-ray crystallography. In the last couple of years, the resolution of macromolecular structures determined by cryo-electron microscopy (cryo-EM) has been drastically improved due to multiple technical advances, allowing us to visualize heterogenous and large assembly of macromolecular complexes. We will use structural biology methods including both cryo-EM and X-ray crystallography together with other biochemical approaches to visualize these transient interactions and investigate their effects for transcription process. Major targets of our study are: 1) the interaction between the Escherichia coli RNA polymerase and DksA/ppGpp for transcription regulation during the stringent response; 2) the interaction between bacterial RNA polymerase and ATP-dependent motor enzyme for rescuing stalled RNA polymerase at the end of transcription cycle; and 3) the interaction between archaeal RNA polymerase and ATP-dependent transcription termination factor Eta for disrupting a stalled transcription elongation complex to initiate the transcription-coupled DNA repair.

项目摘要 我们研究的长期目标是了解细胞RNA聚合酶的转录机制。 我们的研究为在不同阶段提供RNA聚合酶的结构做出了重大贡献 转录周期。在接下来的五年中，我们将继续研究转录机械 细菌和古细菌可提供转录基本机制的见解，这是保守的 从细菌到人。 在过去的20年中，X射线晶体学在RNA的结构生物学中发挥了重要作用 聚合酶并揭示了许多重要的结构。主流的明显阶段的RNA聚合酶 转录周期的中通常称为RNA聚合酶核心酶，全酶，开放式复合物 具有强大的启动子，转录启动和伸长复合物。这些结构很好 由于其稳定的本质而被特征。细胞RNA聚合酶结构生物学的挑战是 可视化RNA聚合酶与其他调节因子和配体发生的瞬时相互作用 在主流或主流的分支路径中的每个明显阶段之间 转录周期。由于它们难以捉摸的本质，这种大分子组件的结晶具有 曾经是瓶颈，因此通过X射线晶体学限制了方法。 在过去的几年中，由冷冻电子确定的大分子结构的分辨率 由于多次技术进步，显微镜（Cryo-EM）已大大改善，使我们能够 可视化大分子复合物的异质和大型组装。我们将使用结构生物学 包括冷冻EM和X射线晶体学在内的方法以及其他生化方法 可视化这些瞬态相互作用并研究它们对转录过程的影响。主要目标 我们的研究是：1）大肠杆菌RNA聚合酶与DKSA/PPGPP之间的相互作用 在严格响应期间的转录调节； 2）细菌RNA聚合酶之间的相互作用 和依赖ATP的运动酶，用于在转录周期结束时营救停滞的RNA聚合酶； 3）古细菌RNA聚合酶与ATP依赖性转录终止之间的相互作用 因子ETA破坏失速的转录伸长复合物以启动转录耦合DNA 维修。