Rodríguez D, Esteban M, Rodríguez J R
Department of Molecular and Cellular Biology, Universidad Autónoma, Madrid, Spain.
J Virol. 1995 Aug;69(8):4640-8. doi: 10.1128/JVI.69.8.4640-4648.1995.
Vaccinia virus (VV) A17L gene encodes a 23-kDa protein that is proteolytically cleaved to generate a 21-kDa product that is incorporated into the viral particles. We have previously shown that the 21-kDa protein forms a stable complex with the VV 14-kDa envelope protein and suggested that the 21-kDa protein may serve to anchor the 14-kDa protein to the envelope of the virion (D. Rodríguez, J. R. Rodríguez, and M. Esteban, J. Virol. 67:3435-3440, 1993). To study the role of the 21-kDa protein in virion assembly, in this investigation we generated a VV recombinant, VVindA17L, that contains an inducible A17L gene regulated by the E. coli repressor/operator system. In the absence of the inducer, shutoff of the A17L gene was complete, and this shutoff correlated with a reduction in virus yields of about 3 log units. Although early and late viral polypeptides are normally synthesized in the absence of the A17L gene product, proteolytic processing of the major p4a and p4b core proteins was clearly impaired under these conditions. Electron microscopy examination of cells infected in the absence of isopropylthiogalactopyranoside (IPTG) revealed that virion morphogenesis was completely arrested at a very early stage, even prior to the formation of crescent-shaped membranes, which are the first distinguishable viral structures. Only electron-dense structures similar to rifampin bodies, but devoid of membranes, could be observed in the cytoplasm of cells infected with VVindA17L under nonpermissive conditions. Considering the most recent assembly model presented by Sodeik et al. (B. Sodeik, R. W. Doms, M. Ericsson, G. Hiller, C. E. Machamer, W. van't Hof, G. van Meer, B. Moss, and G. Griffiths, J. Cell Biol. 121:521-541, 1993), we propose that this protein is targeted to the intermediate compartment and is involved in the recruitment of these membranes to the viral factories, where it forms the characteristic crescent structures that subsequently result in the formation of virions.
痘苗病毒(VV)的A17L基因编码一种23 kDa的蛋白质,该蛋白质经蛋白水解切割后产生一种21 kDa的产物,并被整合到病毒颗粒中。我们之前已经表明,这种21 kDa的蛋白质与VV 14 kDa的包膜蛋白形成稳定的复合物,并推测该21 kDa的蛋白质可能用于将14 kDa的蛋白质锚定到病毒粒子的包膜上(D. Rodríguez、J. R. Rodríguez和M. Esteban,《病毒学杂志》67:3435 - 3440,1993年)。为了研究这种21 kDa蛋白质在病毒粒子组装中的作用,在本研究中,我们构建了一种VV重组体,即VVindA17L,它含有一个受大肠杆菌阻遏物/操纵子系统调控的可诱导A17L基因。在没有诱导剂的情况下,A17L基因的关闭是完全的,并且这种关闭与病毒产量降低约3个对数单位相关。尽管在没有A17L基因产物的情况下通常会合成早期和晚期病毒多肽,但在这些条件下,主要的p4a和p4b核心蛋白的蛋白水解加工明显受损。对在没有异丙基硫代半乳糖苷(IPTG)的情况下感染的细胞进行电子显微镜检查发现,病毒粒子的形态发生在非常早期阶段就完全停滞,甚至在新月形膜形成之前,新月形膜是最早可区分的病毒结构。在非允许条件下,用VVindA17L感染的细胞的细胞质中只能观察到类似于利福平体但没有膜的电子致密结构。考虑到Sodeik等人提出的最新组装模型(B. Sodeik、R. W. Doms、M. Ericsson、G. Hiller、C. E. Machamer、W. van't Hof、G. van Meer、B. Moss和G. Griffiths,《细胞生物学杂志》121:521 - 541,1993年),我们提出这种蛋白质被靶向到中间区室,并参与将这些膜募集到病毒工厂,在那里它形成特征性的新月形结构,随后导致病毒粒子的形成。