Hu X, Wolffe E J, Weisberg A S, Carroll L J, Moss B
Laboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland 20892-0445, USA.
J Virol. 1998 Jan;72(1):104-12. doi: 10.1128/JVI.72.1.104-112.1998.
The vaccinia virus early transcription factor (VETF) is a DNA binding protein comprised of 70- and 82-kDa subunits encoded by the D6R and A8L genes, respectively. A previous investigation suggested a novel role for the 70-kDa subunit in the morphogenesis of vaccinia virus particles. The principal objectives of the present study were to determine if the 82-kDa subunit of VETF is also required for morphogenesis and, if so, whether the block occurs before or after the incorporation of the genome into the assembling virus particle. To address these and other questions, we constructed and characterized a conditionally lethal recombinant vaccinia virus in which the A8L gene is stringently repressed by the Escherichia coli lac operator system. The amount of 82-kDa protein synthesized could be regulated by the amount of inducer: from undetectable to higher than normal levels. Virus replication, as determined by plaque formation or virus yield upon synchronous infection, was dependent on inducer. Nevertheless, de novo synthesis of the 82-kDa subunit was not required for viral early, intermediate, and late gene expression or DNA replication. Overexpression of the A8L gene alone, produced by high concentrations of inducer, inhibited viral late protein synthesis, whereas overexpression of the D6R gene alone or both VETF genes simultaneously had little inhibitory effect. Laser confocal fluorescence and quantitative electron microscopic analyses revealed that immature and DNA-containing intermediate stage particles accumulated in the absence of inducer, indicating that the A8L protein has a role in morphogenesis of the core and subsequent events.
痘苗病毒早期转录因子(VETF)是一种DNA结合蛋白,由分别由D6R和A8L基因编码的70 kDa和82 kDa亚基组成。先前的一项研究表明,70 kDa亚基在痘苗病毒颗粒的形态发生中具有新的作用。本研究的主要目的是确定VETF的82 kDa亚基是否也是形态发生所必需的,如果是,该阻断发生在基因组整合到组装的病毒颗粒之前还是之后。为了解决这些以及其他问题,我们构建并鉴定了一种条件致死性重组痘苗病毒,其中A8L基因受到大肠杆菌乳糖操纵子系统的严格抑制。合成的82 kDa蛋白的量可以通过诱导剂的量来调节:从不可检测到高于正常水平。通过噬斑形成或同步感染后的病毒产量确定的病毒复制依赖于诱导剂。然而,病毒早期、中期和晚期基因表达或DNA复制并不需要从头合成82 kDa亚基。高浓度诱导剂单独产生的A8L基因过表达抑制病毒晚期蛋白合成,而单独的D6R基因过表达或两个VETF基因同时过表达几乎没有抑制作用。激光共聚焦荧光和定量电子显微镜分析表明,在没有诱导剂的情况下,未成熟和含DNA的中间阶段颗粒会积累,这表明A8L蛋白在核心的形态发生及后续事件中起作用。