Department of Infection Biology, Graduate School of Comprehensive Human Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba 305-8575, Japan.
J Virol. 2011 Jul;85(13):6197-204. doi: 10.1128/JVI.00277-11. Epub 2011 Apr 20.
The influenza virus RNA-dependent RNA polymerase is capable of initiating replication but mainly catalyzes abortive RNA synthesis in the absence of viral and host regulatory factors. Previously, we reported that IREF-1/minichromosome maintenance (MCM) complex stimulates a de novo initiated replication reaction by stabilizing an initiated replication complex through scaffolding between the viral polymerase and nascent cRNA to which MCM binds. In addition, several lines of genetic and biochemical evidence suggest that viral nucleoprotein (NP) is involved in successful replication. Here, using cell-free systems, we have shown the precise stimulatory mechanism of virus genome replication by NP. Stepwise cell-free replication reactions revealed that exogenously added NP free of RNA activates the viral polymerase during promoter escape while it is incapable of encapsidating the nascent cRNA. However, we found that a previously identified cellular protein, RAF-2p48/NPI-5/UAP56, facilitates replication reaction-coupled encapsidation as an NP molecular chaperone. These findings demonstrate that replication of the virus genome is followed by its encapsidation by NP in collaboration with its chaperone.
流感病毒 RNA 依赖性 RNA 聚合酶能够起始复制,但在缺乏病毒和宿主调节因子的情况下,主要催化无意义的 RNA 合成。之前,我们报道称 IREF-1/ 微小染色体维持 (MCM) 复合物通过在病毒聚合酶和新生 cRNA 之间形成支架,将 MCM 结合到新生 cRNA 上,从而稳定起始复制复合物,从而刺激从头开始的复制反应。此外,有几条遗传和生化证据表明,病毒核蛋白 (NP) 参与了成功的复制。在这里,我们使用无细胞系统展示了 NP 对病毒基因组复制的精确刺激机制。逐步的无细胞复制反应表明,在启动子逃避过程中,外源添加的无 RNA 的 NP 可激活病毒聚合酶,而 NP 不能包裹新生的 cRNA。然而,我们发现先前鉴定的一种细胞蛋白 RAF-2p48/NPI-5/UAP56 作为 NP 分子伴侣促进复制反应偶联的包装。这些发现表明,病毒基因组的复制随后是由 NP 与其伴侣蛋白共同进行的包装。