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本文引用的文献

1
X-linked RNA-binding motif protein (RBMX) is required for the maintenance of Borna disease virus nuclear viral factories.X连锁RNA结合基序蛋白(RBMX)是维持博尔纳病病毒核病毒工厂所必需的。
J Gen Virol. 2015 Nov;96(11):3198-3203. doi: 10.1099/jgv.0.000273. Epub 2015 Sep 1.
2
Highly condensed chromatins are formed adjacent to subtelomeric and decondensed silent chromatin in fission yeast.在裂殖酵母中,高度浓缩的染色质在亚端粒和去浓缩的沉默染色质附近形成。
Nat Commun. 2015 Jul 24;6:7753. doi: 10.1038/ncomms8753.
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Architecture and biogenesis of plus-strand RNA virus replication factories.正链RNA病毒复制工厂的结构与生物发生
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4
Analysis of borna disease virus trafficking in live infected cells by using a virus encoding a tetracysteine-tagged p protein.利用编码四肽标签化 p 蛋白的病毒分析活感染细胞中的博尔纳病病毒运输。
J Virol. 2013 Nov;87(22):12339-48. doi: 10.1128/JVI.01127-13. Epub 2013 Sep 11.
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The spatio-temporal distribution dynamics of Ebola virus proteins and RNA in infected cells.感染细胞中埃博拉病毒蛋白和 RNA 的时空分布动态。
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Ultrabright photoactivatable fluorophores created by reductive caging.通过还原笼蔽作用产生的超高亮光活化荧光团。
Nat Methods. 2012 Dec;9(12):1181-4. doi: 10.1038/nmeth.2214. Epub 2012 Oct 28.
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RBMX: a regulator for maintenance and centromeric protection of sister chromatid cohesion.RBMX:姐妹染色单体黏合的维持和着丝粒保护的调控因子。
Cell Rep. 2012 Apr 19;1(4):299-308. doi: 10.1016/j.celrep.2012.02.005. Epub 2012 Mar 22.
8
Bornavirus closely associates and segregates with host chromosomes to ensure persistent intranuclear infection.细小病毒与宿主染色体紧密关联和分离,以确保持续的核内感染。
Cell Host Microbe. 2012 May 17;11(5):492-503. doi: 10.1016/j.chom.2012.04.009.
9
Ultrastructural characterization of arterivirus replication structures: reshaping the endoplasmic reticulum to accommodate viral RNA synthesis.动脉病毒复制结构的超微结构特征:重塑内质网以适应病毒 RNA 合成。
J Virol. 2012 Mar;86(5):2474-87. doi: 10.1128/JVI.06677-11. Epub 2011 Dec 21.
10
DAOSTORM: an algorithm for high- density super-resolution microscopy.DAOSTORM:一种用于高密度超分辨率显微镜的算法。
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博尔纳病病毒在细胞核中组装成多孔笼状病毒工厂。

Borna Disease Virus Assembles Porous Cage-like Viral Factories in the Nucleus.

作者信息

Hirai Yuya, Hirano Yasuhiro, Matsuda Atsushi, Hiraoka Yasushi, Honda Tomoyuki, Tomonaga Keizo

机构信息

From the Department of Biology, Osaka Dental University, Hirakata 573-1121.

the Department of Virus Research, Institute for Frontier Life and Medical Sciences (InFRONT).

出版信息

J Biol Chem. 2016 Dec 9;291(50):25789-25798. doi: 10.1074/jbc.M116.746396. Epub 2016 Nov 1.

DOI:10.1074/jbc.M116.746396
PMID:27803166
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5207054/
Abstract

Animal-derived RNA viruses frequently generate viral factories in infected cells. However, the details of how RNA viruses build such intracellular structures are poorly understood. In this study, we examined the structure and formation of the viral factories, called viral speckle of transcripts (vSPOTs), that are produced in the nuclei of host cells by Borna disease virus (BDV). Super-resolution microscopic analysis showed that BDV assembled vSPOTs as intranuclear cage-like structures with 59-180-nm pores. The viral nucleoprotein formed the exoskeletons of vSPOTs, whereas the other viral proteins appeared to be mainly localized within these structures. In addition, stochastic optical reconstruction microscopy revealed that filamentous structures resembling viral ribonucleoprotein complexes (RNPs) appeared to protrude from the outer surfaces of the vSPOTs. We also found that vSPOTs disintegrated into RNPs concurrently with the breakdown of the nuclear envelope during mitosis. These observations demonstrated that BDV generates viral replication factories whose shape and formation are regulated, suggesting the mechanism of the integrity of RNA virus persistent infection in the nucleus.

摘要

动物源RNA病毒经常在受感染细胞中形成病毒工厂。然而,RNA病毒如何构建这种细胞内结构的细节却知之甚少。在本研究中,我们研究了由博尔纳病病毒(BDV)在宿主细胞核中产生的病毒工厂——转录本病毒斑点(vSPOTs)的结构和形成。超分辨率显微镜分析表明,BDV将vSPOTs组装成具有59 - 180纳米孔隙的核内笼状结构。病毒核蛋白形成了vSPOTs的外骨架,而其他病毒蛋白似乎主要定位于这些结构内。此外,随机光学重建显微镜显示,类似于病毒核糖核蛋白复合体(RNPs)的丝状结构似乎从vSPOTs的外表面突出。我们还发现,在有丝分裂期间,随着核膜的破裂,vSPOTs解体为RNPs。这些观察结果表明,BDV产生了形状和形成受到调控的病毒复制工厂,提示了RNA病毒在细胞核中持续感染的完整性机制。