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细胞因子NXP2/MORC3是流感病毒增殖的正向调节因子。

The Cellular Factor NXP2/MORC3 Is a Positive Regulator of Influenza Virus Multiplication.

作者信息

Ver Lorena S, Marcos-Villar Laura, Landeras-Bueno Sara, Nieto Amelia, Ortín Juan

机构信息

Centro Nacional de Biotecnología (CSIC), Darwin 3, Madrid, Spain CIBER de Enfermedades Respiratorias, ISCIII, Madrid, Spain.

Centro Nacional de Biotecnología (CSIC), Darwin 3, Madrid, Spain CIBER de Enfermedades Respiratorias, ISCIII, Madrid, Spain

出版信息

J Virol. 2015 Oct;89(19):10023-30. doi: 10.1128/JVI.01530-15. Epub 2015 Jul 22.

Abstract

UNLABELLED

Transcription and replication of influenza A virus are carried out in the nuclei of infected cells in the context of viral ribonucleoproteins (RNPs). The viral polymerase responsible for these processes is a protein complex composed of the PB1, PB2, and PA proteins. We previously identified a set of polymerase-associated cellular proteins by proteomic analysis of polymerase-containing intracellular complexes expressed and purified from human cells. Here we characterize the role of NXP2/MORC3 in the infection cycle. NXP2/MORC3 is a member of the Microrchidia (MORC) family that is associated with the nuclear matrix and has RNA-binding activity. Influenza virus infection led to a slight increase in NXP2/MORC3 expression and its partial relocalization to the cytoplasm. Coimmunoprecipitation and immunofluorescence experiments indicated an association of NXP2/MORC3 with the viral polymerase and RNPs during infection. Downregulation of NXP2/MORC3 by use of two independent short hairpin RNAs (shRNAs) reduced virus titers in low-multiplicity infections. Consistent with these findings, analysis of virus-specific RNA in high-multiplicity infections indicated a reduction of viral RNA (vRNA) and mRNA after NXP2/MORC3 downregulation. Silencing of NXP2/MORC3 in a recombinant minireplicon system in which virus transcription and replication are uncoupled showed reductions in cat mRNA and chloramphenicol acetyltransferase (CAT) protein accumulation but no alterations in cat vRNA levels, suggesting that NXP2/MORC3 is important for influenza virus transcription.

IMPORTANCE

Influenza virus infections appear as yearly epidemics and occasional pandemics of respiratory disease, with high morbidity and occasional mortality. Influenza viruses are intracellular parasites that replicate and transcribe their genomic ribonucleoproteins in the nuclei of infected cells, in a complex interplay with host cell factors. Here we characterized the role of the human NXP2/MORC3 protein, a member of the Microrchidia family that is associated with the nuclear matrix, during virus infection. NXP2/MORC3 associates with the viral ribonucleoproteins in infected cells. Downregulation of NXP2/MORC3 reduced virus titers and accumulations of viral genomic RNA and mRNAs. Silencing of NXP2/MORC3 in an influenza virus CAT minireplicon system diminished CAT protein and cat mRNA levels but not genomic RNA levels. We propose that NXP2/MORC3 plays a role in influenza virus transcription.

摘要

未标记

甲型流感病毒的转录和复制在病毒核糖核蛋白(RNP)的背景下于受感染细胞的细胞核中进行。负责这些过程的病毒聚合酶是一种由PB1、PB2和PA蛋白组成的蛋白质复合物。我们之前通过对从人细胞中表达和纯化的含聚合酶的细胞内复合物进行蛋白质组学分析,鉴定出了一组与聚合酶相关的细胞蛋白。在此,我们描述了NXP2/MORC3在感染周期中的作用。NXP2/MORC3是微精蛋白(MORC)家族的成员,与核基质相关且具有RNA结合活性。流感病毒感染导致NXP2/MORC3表达略有增加,并使其部分重新定位到细胞质中。免疫共沉淀和免疫荧光实验表明,在感染期间NXP2/MORC3与病毒聚合酶和RNP相关联。使用两种独立的短发夹RNA(shRNA)下调NXP2/MORC3可降低低倍感染中的病毒滴度。与这些发现一致,在高倍感染中对病毒特异性RNA的分析表明,下调NXP2/MORC3后病毒RNA(vRNA)和mRNA减少。在病毒转录和复制解偶联的重组微型复制子系统中沉默NXP2/MORC3,显示cat mRNA和氯霉素乙酰转移酶(CAT)蛋白积累减少,但cat vRNA水平没有改变,这表明NXP2/MORC3对流感病毒转录很重要。

重要性

流感病毒感染表现为每年的呼吸道疾病流行以及偶尔的大流行,发病率高且偶有死亡。流感病毒是细胞内寄生虫,在受感染细胞的细胞核中复制并转录其基因组核糖核蛋白,与宿主细胞因子存在复杂的相互作用。在此,我们描述了人类NXP2/MORC3蛋白(微精蛋白家族的成员,与核基质相关)在病毒感染期间的作用。NXP2/MORC3在受感染细胞中与病毒核糖核蛋白相关联。下调NXP2/MORC3可降低病毒滴度以及病毒基因组RNA和mRNA的积累。在流感病毒CAT微型复制子系统中沉默NXP2/MORC3可降低CAT蛋白和cat mRNA水平,但不影响基因组RNA水平。我们认为NXP2/MORC3在流感病毒转录中发挥作用。

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