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2
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The E6 protein from vaccinia virus is required for the formation of immature virions.牛痘病毒的 E6 蛋白对于不成熟病毒粒子的形成是必需的。
Virology. 2010 Apr 10;399(2):201-11. doi: 10.1016/j.virol.2010.01.012. Epub 2010 Feb 8.

本文引用的文献

1
The E6 protein from vaccinia virus is required for the formation of immature virions.牛痘病毒的 E6 蛋白对于不成熟病毒粒子的形成是必需的。
Virology. 2010 Apr 10;399(2):201-11. doi: 10.1016/j.virol.2010.01.012. Epub 2010 Feb 8.
2
Expression of the highly conserved vaccinia virus E6 protein is required for virion morphogenesis.痘病毒高度保守的E6蛋白的表达是病毒粒子形态发生所必需的。
Virology. 2009 Apr 10;386(2):478-85. doi: 10.1016/j.virol.2009.01.009. Epub 2009 Feb 12.
3
Marker rescue mapping of the combined Condit/Dales collection of temperature-sensitive vaccinia virus mutants.对温度敏感痘苗病毒突变体的Condit/Dales联合文库进行标记拯救定位
Virology. 2008 May 25;375(1):213-22. doi: 10.1016/j.virol.2008.01.027. Epub 2008 Mar 7.
4
The vaccinia virus E8R gene product is required for formation of transcriptionally active virions.痘苗病毒E8R基因产物是形成转录活性病毒粒子所必需的。
Virology. 2007 Oct 25;367(2):398-412. doi: 10.1016/j.virol.2007.05.002. Epub 2007 Jul 9.
5
In a nutshell: structure and assembly of the vaccinia virion.简而言之:痘苗病毒粒子的结构与组装。
Adv Virus Res. 2006;66:31-124. doi: 10.1016/S0065-3527(06)66002-8.
6
Vaccinia virus proteolysis--a review.痘苗病毒蛋白水解——综述
Rev Med Virol. 2006 May-Jun;16(3):187-202. doi: 10.1002/rmv.499.
7
Vaccinia virus proteome: identification of proteins in vaccinia virus intracellular mature virion particles.痘苗病毒蛋白质组:痘苗病毒细胞内成熟病毒粒子中蛋白质的鉴定
J Virol. 2006 Mar;80(5):2127-40. doi: 10.1128/JVI.80.5.2127-2140.2006.
8
The conserved poxvirus L3 virion protein is required for transcription of vaccinia virus early genes.保守的痘病毒L3病毒粒子蛋白是牛痘病毒早期基因转录所必需的。
J Virol. 2005 Dec;79(23):14719-29. doi: 10.1128/JVI.79.23.14719-14729.2005.
9
External scaffold of spherical immature poxvirus particles is made of protein trimers, forming a honeycomb lattice.球形未成熟痘病毒颗粒的外部支架由蛋白质三聚体组成,形成蜂窝状晶格。
J Cell Biol. 2005 Sep 12;170(6):971-81. doi: 10.1083/jcb.200504026. Epub 2005 Sep 6.
10
Deep-etch EM reveals that the early poxvirus envelope is a single membrane bilayer stabilized by a geodetic "honeycomb" surface coat.深度蚀刻电子显微镜显示,早期痘病毒包膜是由大地测量学上的“蜂窝状”表面涂层稳定的单膜双层结构。
J Cell Biol. 2005 Apr 25;169(2):269-83. doi: 10.1083/jcb.200412169.

温度敏感型突变体在痘苗病毒 E6 蛋白产生转录失活的病毒粒子。

Temperature-sensitive mutant in the vaccinia virus E6 protein produce virions that are transcriptionally inactive.

机构信息

Department of Molecular Genetics and Microbiology, University of Florida, Gainesville, FL 32610, USA.

出版信息

Virology. 2010 Apr 10;399(2):221-30. doi: 10.1016/j.virol.2010.01.010. Epub 2010 Feb 8.

DOI:10.1016/j.virol.2010.01.010
PMID:20116822
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2830351/
Abstract

The vaccinia virus E6R gene encodes a late protein that is packaged into virion cores. A temperature-sensitive mutant was used to study the role of this protein in viral replicative cycle. Cts52 has a P226L missense mutation in the E6R gene, shows a two-log reduction in plaque formation, but displays normal patterns of gene expression, late protein processing and DNA replication during infection. Mutant virions produced at 40 degrees C were similar in their morphology to wt virions grown at 40 degrees C. The particle to infectivity ratio was 50 times higher in purified Cts52 grown at 40 degrees C when compared to the mutant grown at permissive temperature. In vitro characterization of Cts-52 particles grown at 40 degrees C revealed no differences in protein composition or in DNA content and the mutant virions could bind and enter cells. However, core particles prepared from Cts52 grown at 40 degrees C failed to transcribe in vitro. Our results show that E6 in the virion has either a direct or an indirect role in viral transcription.

摘要

痘苗病毒 E6R 基因编码一种晚期蛋白,该蛋白被包装到病毒核心中。使用温度敏感突变体来研究该蛋白在病毒复制周期中的作用。Cts52 在 E6R 基因中具有 P226L 错义突变,其在斑块形成方面减少了两个对数,但在感染过程中显示出正常的基因表达、晚期蛋白加工和 DNA 复制模式。在 40°C 下产生的突变病毒粒子在形态上与在 40°C 下生长的 wt 病毒粒子相似。与在允许温度下生长的突变体相比,在 40°C 下生长的纯化 Cts52 的颗粒与感染性之比高 50 倍。在 40°C 下生长的 Cts-52 颗粒的体外特性分析表明,在蛋白质组成或 DNA 含量方面没有差异,并且突变体病毒粒子可以结合并进入细胞。然而,从在 40°C 下生长的 Cts52 制备的核心颗粒无法在体外转录。我们的结果表明,病毒粒子中的 E6 要么直接要么间接参与病毒转录。