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The Interactomes of Influenza Virus NS1 and NS2 Proteins Identify New Host Factors and Provide Insights for ADAR1 Playing a Supportive Role in Virus Replication

机译:流感病毒NS1和NS2蛋白的相互作用组识别新的宿主因子,并为ADAR1在病毒复制中起支持作用提供见解

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Influenza A NS1 and NS2 proteins are encoded by the RNA segment 8 of the viral genome. NS1 is a multifunctional protein and a virulence factor while NS2 is involved in nuclear export of viral ribonucleoprotein complexes. A yeast two-hybrid screening strategy was used to identify host factors supporting NS1 and NS2 functions. More than 560 interactions between 79 cellular proteins and NS1 and NS2 proteins from 9 different influenza virus strains have been identified. These interacting proteins are potentially involved in each step of the infectious process and their contribution to viral replication was tested by RNA interference. Validation of the relevance of these host cell proteins for the viral replication cycle revealed that 7 of the 79 NS1 and/or NS2-interacting proteins positively or negatively controlled virus replication. One of the main factors targeted by NS1 of all virus strains was double-stranded RNA binding domain protein family. In particular, adenosine deaminase acting on RNA 1 (ADAR1) appeared as a pro-viral host factor whose expression is necessary for optimal viral protein synthesis and replication. Surprisingly, ADAR1 also appeared as a pro-viral host factor for dengue virus replication and directly interacted with the viral NS3 protein. ADAR1 editing activity was enhanced by both viruses through dengue virus NS3 and influenza virus NS1 proteins, suggesting a similar virus-host co-evolution.
机译:甲型流感病毒NS1和NS2蛋白由病毒基因组的RNA片段8编码。 NS1是一种多功能蛋白和一种致病因子,而NS2则参与病毒核糖核蛋白复合物的核输出。酵母双杂交筛选策略用于识别支持NS1和NS2功能的宿主因子。已经鉴定出79种细胞蛋白与来自9种不同流感病毒株的NS1和NS2蛋白之间的超过560种相互作用。这些相互作用的蛋白质可能参与感染过程的每个步骤,并通过RNA干扰测试了它们对病毒复制的贡献。这些宿主细胞蛋白与病毒复制周期的相关性验证表明,在79种与NS1和/或与NS2相互作用的蛋白中,有7种正向或反向控制病毒复制。所有病毒株的NS1靶向的主要因素之一是双链RNA结合域蛋白家族。特别是,作用于RNA 1(ADAR1)的腺苷脱氨酶是一种前病毒宿主因子,其表达对于优化病毒蛋白的合成和复制是必需的。出人意料的是,ADAR1还作为登革热病毒复制的前病毒宿主因子出现,并直接与病毒NS3蛋白相互作用。两种病毒都通过登革热病毒NS3和流感病毒NS1蛋白增强了ADAR1的编辑活性,表明病毒-宿主共同进化。

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