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Nuclear dynamics of influenza A virus ribonucleoproteins revealed by live-cell imaging studies

机译:活细胞成像研究揭示了甲型流感病毒核糖核蛋白的核动力学

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摘要

The negative sense RNA genome of influenza A virus is transcribed and replicated in the nuclei of infected cells by the viral RNA polymerase. Only four viral polypeptides are required but multiple cellular components are potentially involved. We used fluorescence recovery after photobleaching (FRAP) to characterise the dynamics of GFP-tagged viral ribonucleoprotein (RNP) components in living cells. The nucleoprotein (NP) displayed very slow mobility that significantly increased on formation of transcriptionally active RNPs. Conversely, single or dimeric polymerase subunits showed fast nuclear dynamics that decreased upon formation of heterotrimers, suggesting increased interaction of the full polymerase complex with a relatively immobile cellular component(s). Treatment with inhibitors of cellular transcription indicated that in part, this reflected an interaction with cellular RNA polymerase II. Analysis of mutated influenza virus polymerase complexes further suggested that this was through an interaction between PB2 and RNA Pol II separate from PB2 cap-binding activity.
机译:甲型流感病毒的负义RNA基因组被病毒RNA聚合酶转录并复制到受感染细胞的核中。仅需要四个病毒多肽,但是可能涉及多个细胞成分。我们使用漂白后的荧光恢复(FRAP)来表征活细胞中带有GFP标签的病毒核糖核蛋白(RNP)组件的动力学。核蛋白(NP)表现出非常慢的迁移率,在转录活性RNP形成时会显着增加。相反,单一或二聚体聚合酶亚基显示出快速的核动力学,该动力学在异源三聚体形成时降低,表明完整聚合酶复合物与相对固定的细胞组分的相互作用增加。用细胞转录抑制剂处理表明,这部分反映了与细胞RNA聚合酶II的相互作用。对突变的流感病毒聚合酶复合物的分析进一步表明,这是通过PB2和RNA POL II之间的相互作用而实现的,而PB2帽结合活性是独立的。

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