Structural Biochemistry of Coordinated DNA Damage Repair Pathways

协调 DNA 损伤修复途径的结构生物化学

• 批准号: RGPIN-2015-05776
• 负责人: Pascal, John
• 金额: $ 2.48万
• 依托单位: Université de Montréal
• 依托单位国家: 加拿大
• 项目类别: Discovery Grants Program - Individual
• 财政年份: 2019
• 资助国家: 加拿大
• 起止时间: 2019-01-01 至 2020-12-31
• 项目状态: 已结题
• 来源: https://www.nserc-crsng.gc.ca/ase-oro/Details-Detailles_eng.asp?id=685375
• 关键词: Structural; Biochemistry; Coordinated; DNA; Damage

The long-term goal of our research program is to advance our fundamental understanding of the molecular mechanisms that underlie the coordinated action of macromolecules in biological signaling and processing pathways. Currently our focus is on the molecular underpinnings of macromolecules that orchestrate detection and repair of cellular DNA damage. All domains of life require DNA damage surveillance and repair mechanisms to preserve the integrity of the genome and thus the fitness of an organism and future generations. Our laboratory is investigating the proteins that carry out DNA damage repair, and we are currently studying the ligation repair of DNA breaks, a common final step in all pathways of DNA damage repair. We have chosen to primarily use the proteins of the thermophilic archaeon Sulfolobus Solfataricus as a model system since it preserves the essential features of eukaryotic repair systems, and the stability and compact domain structures of the proteins makes them well suited for structural analysis. Like in many organisms, S. Solfataricus DNA ligase activity is coordinated by a DNA sliding clamp protein called PCNA (proliferating cell nuclear antigen); however, the molecular basis for the coordinated action of ligase and PCNA is poorly understood. Our research program will work toward a molecular level understanding of the ligase-PCNA interaction through the use of structural biology techniques and biochemical analysis. In particular, we will investigate the conformational changes associated with the three-step mechanism of DNA ligation, and how PCNA coordinates these conformational changes. DNA damage repair requires the coordinated action of multiple enzymes, and our studies will provide key insights into how the activity of DNA ligase is coordinated by the master regulator PCNA. Notably, S. Solfataricus PCNA binds multiple components of the repair machinery (polymerase, nuclease, ligase) and thus will allow us over time to expand our analysis to the coordinated action of multiple enzymes in a complex repair pathway. The proposed research is essential to advance our fundamental understanding of the mechanisms underlying the cellular repair of DNA damage. These findings ultimately can contribute to the development of methods to disrupt efficient repair, for example in cancer cells that must cope with an inherently unstable genome and thus depend on efficient repair mechanisms.**

我们研究计划的长期目标是推进我们对生物信号传导和加工途径中大分子协调作用的分子机制的基本理解。目前，我们的重点是大分子的分子基础，协调检测和修复细胞DNA损伤。生命的所有领域都需要DNA损伤监测和修复机制来保持基因组的完整性，从而保持生物体和后代的健康。我们的实验室正在研究进行DNA损伤修复的蛋白质，我们目前正在研究DNA断裂的连接修复，这是所有DNA损伤修复途径中常见的最后一步。我们选择主要使用嗜热古菌Sulfolobus Solfataricus的蛋白质作为模型系统，因为它保留了真核修复系统的基本特征，并且蛋白质的稳定性和紧凑的结构域结构使其非常适合于结构分析。像许多生物一样，S。Solfataricus DNA连接酶活性由称为PCNA（增殖细胞核抗原）的DNA滑动钳蛋白协调;然而，连接酶和PCNA协调作用的分子基础知之甚少。我们的研究计划将致力于通过使用结构生物学技术和生化分析的连接酶-PCNA相互作用的分子水平的理解。特别是，我们将研究与DNA连接的三步机制相关的构象变化，以及PCNA如何协调这些构象变化。DNA损伤修复需要多种酶的协调作用，我们的研究将提供关键的见解，DNA连接酶的活性是如何协调的主调节PCNA。值得注意的是，S. Solfataricus PCNA结合修复机制的多个组件（聚合酶，核酸酶，连接酶），因此随着时间的推移，将使我们能够将我们的分析扩展到复杂修复途径中多种酶的协调作用。这项研究对于促进我们对DNA损伤细胞修复机制的基本理解至关重要。这些发现最终可以有助于开发破坏有效修复的方法，例如在必须科普固有不稳定基因组的癌细胞中，因此依赖于有效的修复机制。