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痘苗病毒E8R基因产物是形成转录活性病毒粒子所必需的。

The vaccinia virus E8R gene product is required for formation of transcriptionally active virions.

作者信息

Kato Sayuri E M, Condit Richard C, Moussatché Nissin

机构信息

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

出版信息

Virology. 2007 Oct 25;367(2):398-412. doi: 10.1016/j.virol.2007.05.002. Epub 2007 Jul 9.

Abstract

Two vaccinia virus temperature-sensitive mutants were mapped to the E8R gene and subjected to phenotypic characterization. Dts23 contains a missense mutation in the coding region of E8R (L81F), and in Cts19 the initiating methionine codon is changed from ATG to ATA (M1I). The two ts mutants display normal patterns of gene expression and DNA replication during infection. The E8 protein is synthesized exclusively late during infection and packaged into virion cores Western blot analysis revealed that E8 synthesis is reduced in Dts23 infected cells at permissive (31 degrees C) and non-permissive temperature (39.7 degrees C) and absent in Cts19 infection under both conditions. Dts23 virions produced at 39.7 degrees C were indistinguishable in appearance from wt virions. Cts19 fails to produce identifiable viral structures when incubated at 39.7 degrees C. Purified Dts23 virions produced at 39.7 degrees C contain reduced amounts of E8 and have a high particle to infectivity ratio; purified Cts19 virions grown at 31 degrees C also show reduced infectivity and do not contain detectable E8. Dts23 grown at 39.7 degrees C could enter cells but failed to synthesize early mRNA or produce CPE. Soluble extracts from mutant virions were active in a promoter dependent in vitro transcription assay, however intact mutant cores were defective in transcription. We suggest that E8 plays a subtle role in virion core structure that impacts directly or indirectly on core transcription.

摘要

将两种痘苗病毒温度敏感突变体定位到E8R基因并进行表型特征分析。Dts23在E8R编码区含有一个错义突变(L81F),而在Cts19中起始甲硫氨酸密码子从ATG变为ATA(M1I)。这两种温度敏感突变体在感染期间表现出正常的基因表达和DNA复制模式。E8蛋白仅在感染后期合成并包装到病毒粒子核心中。蛋白质印迹分析显示,在允许温度(31℃)和非允许温度(39.7℃)下,Dts23感染的细胞中E8合成减少,并且在两种条件下Cts19感染中均不存在E8合成。在39.7℃产生的Dts23病毒粒子在外观上与野生型病毒粒子无法区分。当在39.7℃孵育时,Cts19无法产生可识别的病毒结构。在39.7℃产生的纯化Dts23病毒粒子含有减少量的E8并且具有高的粒子感染性比率;在31℃生长的纯化Cts19病毒粒子也显示出感染性降低并且不含有可检测到的E8。在39.7℃生长的Dts23可以进入细胞,但未能合成早期mRNA或产生细胞病变效应。来自突变病毒粒子的可溶性提取物在启动子依赖性体外转录测定中具有活性,然而完整的突变核心在转录方面存在缺陷。我们认为E8在病毒粒子核心结构中起微妙作用,直接或间接影响核心转录。

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