Structure and mechanism of CRISPR-Cas type IV systems

CRISPR-Cas IV型系统的结构和机制

• 批准号: 405858511
• 负责人: Professor Dr. Gert Bange
• 金额: --
• 依托单位: Zentrum für Synthetische Mikrobiologie (SYNMIKRO)
• 依托单位国家: 德国
• 项目类别: Priority Programmes
• 资助国家: 德国
• 项目状态: 未结题
• 来源: https://gepris.dfg.de/gepris/projekt/405858511?language=en
• 关键词: Structure; mechanism; CRISPR; Cas; type

CRISPR-Cas systems are structurally and mechanistically highly diverse prokaryotic adaptive immune systems that protect against mobile genetic elements. Class I CRISPR-Cas systems feature multi-subunit effector complexes. We could recently demonstrate that even closely related subtypes, i.e. the type I-F and I-F variant (I-Fv), differ substantially in their structure and DNA surveillance mechanism. Furthermore, CRISPR-Cas systems have been implied to function in non-canonical processes, such as e.g. transcriptional control, stress response and pathogenicity development. Others and we could show that the CRISPR adaptation protein Cas1 interacts with the redox-stress sensing and signaling two-component system YedVW. The aim of this proposal is to produce an en-detail structural, mechanistic and functional understanding of poorly understood class I CRISPR-Cas systems, such as e.g. the Shewanella putrefaciens type I-Fv and the plasmid borne Aromatoleum aromaticum type IV system. Moreover, we aim at a structural, mechanistic and functional understanding of the interaction of Cas1 and YedVW in the redox-stress induced stress response of Escherichia coli.

CRISPR-Cas系统是结构上和机制上高度多样的原核适应性免疫系统，其针对移动的遗传元件进行保护。I类CRISPR-Cas系统的特征在于多亚基效应物复合物。我们最近可以证明，即使是密切相关的亚型，即I-F型和I-F变体（I-Fv），在其结构和DNA监视机制方面也有很大差异。此外，CRISPR-Cas系统已被暗示在非规范过程中起作用，例如转录控制、应激反应和致病性发展。其他人和我们可以证明CRISPR适应蛋白Cas 1与氧化还原应激传感和信号传导双组分系统YedVW相互作用。该提案的目的是对尚不清楚的I类CRISPR-Cas系统（例如腐败希瓦氏菌I-Fv型和质粒携带的芳香族化合物IV型系统）产生详细的结构、机制和功能理解。此外，我们的目标是在结构，机制和功能的理解的相互作用的Cas 1和YedVW在氧化还原应激诱导的应激反应的大肠杆菌。