首页> 外文期刊>Journal of proteome research >Interactome Analysis of NS1 Protein Encoded by Influenza A H7N9 Virus Reveals an Inhibitory Role of NS1 in Host mRNA Maturation
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Interactome Analysis of NS1 Protein Encoded by Influenza A H7N9 Virus Reveals an Inhibitory Role of NS1 in Host mRNA Maturation

机译:流感H7N9病毒编码的NS1蛋白的互乱分析显示NS1在宿主mRNA成熟中的抑制作用

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摘要

Influenza A virus infections can result in severe respiratory diseases. The H7N9 subtype of avian influenza A virus has been transmitted to humans and caused severe disease and death. Nonstructural protein 1 (NS1) of influenza A virus is a virulence determinant during viral infection. To elucidate the functions of the NS1 encoded by influenza A H7N9 virus (H7N9 NS1), interaction partners of H7N9 NS1 in human cells were identified with immunoprecipitation followed by SDS-PAGE coupled with liquid chromatography-tandem mass spectrometry (GeLC–MS/MS). We identified 36 cellular proteins as the interacting partners of the H7N9 NS1, and they are involved in RNA processing, mRNA splicing via spliceosome, and the mRNA surveillance pathway. Two of the interacting partners, cleavage and polyadenylation specificity factor subunit 2 (CPSF2) and CPSF7, were confirmed to interact with H7N9 NS1 using coimmunoprecipitation and immunoblotting based on the previous finding that the two proteins are involved in pre-mRNA polyadenylation machinery. Furthermore, we illustrate that overexpression of H7N9 NS1, as well as infection by the influenza A H7N9 virus, interfered with pre-mRNA polyadenylation in host cells. This study comprehensively profiled the interactome of H7N9 NS1 in host cells, and the results demonstrate a novel endotype for H7N9 NS1 in inhibiting host mRNA maturation.
机译:流感病毒感染可能导致严重的呼吸系统疾病。禽流感的H7N9亚型病毒已传播给人类并引起严重的疾病和死亡。流感的非结构蛋白1(NS1)病毒是病毒感染期间的毒力决定因素。为了阐明由甲型H7N9病毒(H7N9 NS1)编码的NS1的功能(H7N9 NS1),用免疫沉淀鉴定H7N9 NS1中H7N9 NS1的相互作用伴侣,然后用SDS-PAGE与液相色谱 - 串联质谱(GELC-MS / MS)偶联。我们将36个细胞蛋白质鉴定为H7N9 NS1的相互作用伴侣,并且它们参与RNA处理,通过抗抗乳糖组和mRNA监测途径。确认使用CoImMunounopectipitipitipitipitipitipitipition和免疫印迹的两种相互作用伴侣,切割和聚腺苷酸化特异性因子亚基2(CPSF2)和CPSF7使用基于先前发现的两种蛋白质参与所述前mRNA多腺苷酸化机械的影响。此外,我们说明H7N9 NS1的过度表达,以及由流感H7N9病毒感染,干扰宿主细胞中的前mRNA多腺苷酸化。本研究全面地分析了宿主细胞中H7N9 NS1的偶联,结果证明了H7N9 NS1的新型内型抑制宿主mRNA成熟。

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