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本文引用的文献

1
Composition and three-dimensional architecture of the dengue virus replication and assembly sites.登革病毒复制与装配位点的组成及三维结构
Cell Host Microbe. 2009 Apr 23;5(4):365-75. doi: 10.1016/j.chom.2009.03.007.
2
SARS-coronavirus replication is supported by a reticulovesicular network of modified endoplasmic reticulum.严重急性呼吸综合征冠状病毒的复制由修饰内质网的网状囊泡网络支持。
PLoS Biol. 2008 Sep 16;6(9):e226. doi: 10.1371/journal.pbio.0060226.
3
Cholesterol manipulation by West Nile virus perturbs the cellular immune response.西尼罗河病毒对胆固醇的调控扰乱细胞免疫反应。
Cell Host Microbe. 2007 Oct 11;2(4):229-39. doi: 10.1016/j.chom.2007.09.003.
4
West Nile virus-induced cytoplasmic membrane structures provide partial protection against the interferon-induced antiviral MxA protein.西尼罗河病毒诱导的细胞质膜结构对干扰素诱导的抗病毒蛋白MxA提供部分保护。
J Gen Virol. 2007 Nov;88(Pt 11):3013-3017. doi: 10.1099/vir.0.83125-0.
5
Three-dimensional analysis of a viral RNA replication complex reveals a virus-induced mini-organelle.病毒RNA复制复合体的三维分析揭示了一种病毒诱导的微型细胞器。
PLoS Biol. 2007 Sep;5(9):e220. doi: 10.1371/journal.pbio.0050220.
6
West Nile virus strain Kunjin NS5 polymerase is a phosphoprotein localized at the cytoplasmic site of viral RNA synthesis.西尼罗河病毒昆金株NS5聚合酶是一种定位于病毒RNA合成细胞质部位的磷蛋白。
J Gen Virol. 2007 Apr;88(Pt 4):1163-1168. doi: 10.1099/vir.0.82552-0.
7
The non-structural protein 4A of dengue virus is an integral membrane protein inducing membrane alterations in a 2K-regulated manner.登革病毒的非结构蛋白4A是一种整合膜蛋白,以2K调节的方式诱导膜改变。
J Biol Chem. 2007 Mar 23;282(12):8873-82. doi: 10.1074/jbc.M609919200. Epub 2007 Feb 2.
8
Regulated cleavages at the West Nile virus NS4A-2K-NS4B junctions play a major role in rearranging cytoplasmic membranes and Golgi trafficking of the NS4A protein.西尼罗河病毒NS4A-2K-NS4B连接处的调控性切割在重新排列细胞质膜和NS4A蛋白的高尔基体运输中起主要作用。
J Virol. 2006 May;80(9):4623-32. doi: 10.1128/JVI.80.9.4623-4632.2006.
9
Subcellular localization and membrane topology of the Dengue virus type 2 Non-structural protein 4B.登革2型病毒非结构蛋白4B的亚细胞定位及膜拓扑结构
J Biol Chem. 2006 Mar 31;281(13):8854-63. doi: 10.1074/jbc.M512697200. Epub 2006 Jan 25.
10
NS1 protein secretion during the acute phase of West Nile virus infection.西尼罗河病毒感染急性期的NS1蛋白分泌
J Virol. 2005 Nov;79(22):13924-33. doi: 10.1128/JVI.79.22.13924-13933.2005.

内质网为黄病毒复制复合物的生物发生提供了膜平台。

The endoplasmic reticulum provides the membrane platform for biogenesis of the flavivirus replication complex.

机构信息

Department of Microbiology, La Trobe University, Bundoora, Melbourne 3086, Australia.

出版信息

J Virol. 2010 Oct;84(20):10438-47. doi: 10.1128/JVI.00986-10. Epub 2010 Aug 4.

DOI:10.1128/JVI.00986-10
PMID:20686019
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2950591/
Abstract

The cytoplasmic replication of positive-sense RNA viruses is associated with a dramatic rearrangement of host cellular membranes. These virus-induced changes result in the induction of vesicular structures that envelop the virus replication complex (RC). In this study, we have extended our previous observations on the intracellular location of West Nile virus strain Kunjin virus (WNV(KUN)) to show that the virus-induced recruitment of host proteins and membrane appears to occur at a pre-Golgi step. To visualize the WNV(KUN) replication complex, we performed three-dimensional (3D) modeling on tomograms from WNV(KUN) replicon-transfected cells. These analyses have provided a 3D representation of the replication complex, revealing the open access of the replication complex with the cytoplasm and the fluidity of the complex to the rough endoplasmic reticulum. In addition, we provide data that indicate that a majority of the viral RNA species housed within the RC is in a double-stranded RNA (dsRNA) form.

摘要

正链 RNA 病毒的细胞质复制与宿主细胞膜的剧烈重排有关。这些病毒诱导的变化导致囊泡结构的诱导,这些囊泡结构包裹着病毒复制复合物(RC)。在这项研究中,我们扩展了之前关于西尼罗河病毒株 Kunjin 病毒(WNV(KUN))在细胞内位置的观察结果,表明病毒诱导的宿主蛋白和膜的募集似乎发生在高尔基体前步骤。为了可视化 WNV(KUN)复制复合物,我们对来自 WNV(KUN)复制子转染细胞的断层扫描图像进行了三维(3D)建模。这些分析提供了复制复合物的 3D 表示,揭示了复制复合物与细胞质的开放访问和复合物到粗糙内质网的流动性。此外,我们提供的数据表明,RC 内的大多数病毒 RNA 物种都处于双链 RNA(dsRNA)形式。