Wang Pui, Song Wenjun, Mok Bobo Wing-Yee, Zhao Pengxi, Qin Kun, Lai Alexander, Smith Gavin J D, Zhang Jinxia, Lin Tianwei, Guan Yi, Chen Honglin
Department of Microbiology, The University of Hong Kong, Pokfulam, People's Republic of China.
J Virol. 2009 Aug;83(16):7850-61. doi: 10.1128/JVI.00735-09. Epub 2009 Jun 3.
Interactions between host factors and the viral replication complex play important roles in host adaptation and regulation of influenza virus replication. A cellular protein, nuclear factor 90 (NF90), was copurified with H5N1 viral nucleoprotein (NP) from human cells in which NP was transiently expressed and identified by matrix-assisted laser desorption ionization-time of flight mass spectrometry analysis. In vitro coimmunoprecipitation of NF90 and NP coexpressed in HEK 293T cells or individually expressed in bacterial and HEK 293T cells, respectively, confirmed a direct interaction between NF90 and NP, independent of other subunits of the ribonucleoprotein complex. This interaction was prevented by a mutation, F412A, in the C-terminal region of the NP, indicating that the C-terminal of NP is required for NF90 binding. RNase V treatment did not prevent coprecipitation of NP and NF90, which demonstrates that the interaction is RNA binding independent. After small interfering RNA knockdown of NF90 expression in A549 and HeLa cells, viral polymerase complex activity and virus replication were significantly increased, suggesting that NF90 negatively affects viral replication. Both NP and NF90 colocalized in the nucleus of virus-infected cells during the early phase of infection, suggesting that the interaction between NF90 and NP is an early event in virus replication. Quantitative reverse transcription-PCR showed that NF90 downregulates both viral genome replication and mRNA transcription in infected cells. These results suggest that NF90 inhibits influenza virus replication during the early phase of infection through direct interaction with viral NP.
宿主因子与病毒复制复合体之间的相互作用在宿主适应和流感病毒复制调控中发挥着重要作用。一种细胞蛋白,即核因子90(NF90),在人细胞中与H5N1病毒核蛋白(NP)共纯化,该细胞中NP被瞬时表达,并通过基质辅助激光解吸电离飞行时间质谱分析进行鉴定。在HEK 293T细胞中共表达或分别在细菌和HEK 293T细胞中单独表达的NF90和NP的体外共免疫沉淀,证实了NF90与NP之间的直接相互作用,独立于核糖核蛋白复合体的其他亚基。NP C末端区域的F412A突变可阻止这种相互作用,表明NP的C末端是NF90结合所必需的。核糖核酸酶V处理并不能阻止NP与NF90的共沉淀,这表明这种相互作用不依赖于RNA结合。在A549和HeLa细胞中通过小干扰RNA敲低NF90表达后,病毒聚合酶复合体活性和病毒复制显著增加,表明NF90对病毒复制有负面影响。在感染早期,NP和NF90都在病毒感染细胞的细胞核中共定位,表明NF90与NP之间的相互作用是病毒复制中的早期事件。定量逆转录PCR显示,NF90下调感染细胞中的病毒基因组复制和mRNA转录。这些结果表明,NF90在感染早期通过与病毒NP的直接相互作用抑制流感病毒复制。