Influenza A virus NS1 suppresses nuclear speckles promoted gene expression by inhibition of transcription.

Wolfgang Nacken, Juliane Mayr, André Schreiber, Stephan Ludwig
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Abstract

IAV-NS1 proteins that interact with Cleavage and polyadenylation specific factor 30 are known to inhibit host gene expression. Here we report that in both transfection and infection experiments, a strong attenuation of reporter gene expression is observed when NS1 proteins are fused to protein domains guiding NS1 exclusively to nuclear speckles (NSP). NS1 proteins that are fused to domains that guide them to nuclear or non-nuclear compartments other than NSP show little or no ability to attenuate reporter gene expression. An NSP-localized NS1-effector domain is sufficient to inhibit gene expression. The protein SON is an essential component of NSP. SiRNA-mediated suppression of SON reduced the ability of NS1 to suppress the expression of a reporter gene relative to cells with fully functional NSP. Lastly, we demonstrate that the NS1-mediated suppression relies on transcriptional inhibition. Our data suggest that IAV-NS1 suppresses NSP-promoted gene expression by inhibition of transcription.

甲型流感病毒NS1通过抑制转录抑制核斑点促进基因表达。
已知IAV-NS1蛋白与切割和多聚腺苷化特异性因子30相互作用可抑制宿主基因表达。在转染和感染实验中,我们观察到当NS1蛋白融合到蛋白结构域时,报告基因表达的强烈衰减将引导NS1只进入核斑点(NSP)。NS1蛋白融合到引导其进入核或非核区室的结构域,而非NSP,很少或没有能力减弱报告基因的表达。ns1效应域的nssp定位足以抑制基因表达。SON蛋白是NSP的重要组成部分。相对于功能完备的NSP细胞,sirna介导的SON抑制降低了NS1抑制报告基因表达的能力。最后,我们证明ns1介导的抑制依赖于转录抑制。我们的数据表明,IAV-NS1通过抑制转录来抑制nsp促进的基因表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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