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Real-time analysis of single influenza virus replication complexes reveals large promoter-dependent differences in initiation dynamics

机译:单型流感病毒复合复合物的实时分析揭示了启动动力学的大型启动子依赖性差异

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摘要

The viral RNA (vRNA) genome of influenza viruses is replicated by the RNA-dependent RNA polymerase (RNAP) via a complementary RNA (cRNA) intermediate. The vRNA promoter can adopt multiple conformations when bound by the RNAP. However, the dynamics, determinants, and biological role of these conformations are unknown; further, little is known about cRNA promoter conformations. To probe the RNA conformations adopted during initial replication, we monitored single, surface-immobilized vRNA and cRNA initiation complexes in real-time. Our results show that, while the 3 ' terminus of the vRNA promoter exists in dynamic equilibrium between pre-initiation and initiation conformations, the cRNA promoter exhibited very limited dynamics. Two residues in the proximal 3 ' region of the cRNA promoter (residues absent in the vRNA promoter) allowed the cRNA template strand to reach further into the active site, limiting promoter dynamics. Our results highlight promoter-dependent differences in influenza initiation mechanisms, and advance our understanding of virus replication.
机译:的流感病毒的病毒RNA(vRNA的)基因组是通过经由互补RNA(cRNA的)中间的RNA依赖性RNA聚合酶(RNAP)复制。当由RNA聚合酶结合的vRNA的启动子可以采用多种构象。但是,动态,决定因素,而这些构象的生物学作用是未知的;此外,知之甚少的cRNA子构象。以探测初始复制期间通过的RNA的构象,我们监测实时单,表面固定的的vRNA和cRNA的起始复合物。我们的研究结果表明,虽然在的vRNA启动子的3'末端存在于预起始和起始构象之间的动态平衡,所述cRNA的启动子表现出非常有限的动态。两个残基在cRNA的启动子(残基不存在于的vRNA启动子)允许的cRNA的模板链中以进一步伸入活性位点的近侧3'区域,限制启动子动力学。我们的研究结果强调在流感引发机制启动相关的分歧,并推进我们的病毒复制的理解。

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