Michael E J, Kuck K M, Kinchington P R
Department of Anesthesiology/Critical Care Medicine, University of Pittsburgh, PA 15213, USA.
J Infect Dis. 1998 Nov;178 Suppl 1:S27-33. doi: 10.1086/514273.
The regulation of varicella-zoster virus (VZV) gene expression is largely controlled at the transcriptional level by a few key viral proteins cooperating with one another and with cellular transcription factors. However, the mechanisms involved are largely unclear. To identify the sequences important for the transcriptional regulation of open-reading frame (ORF) 4, itself encoding a transcriptional regulator, a mutation analysis of the promoter was done. These studies identified an element between -69 and -59 (relative to the transcriptional start site), which was critical to the activity of the promoter upon stimulation by the VZV transactivator IE62 and by VZV infection. DNA-protein interaction studies revealed that VZV induced the binding of a specific protein complex to this element, which contained the ubiquitous transcription factor USF. ORF 4 is the second VZV gene (in addition to VZV ORF 29) in which USF binding plays a critical role in gene expression.
水痘带状疱疹病毒(VZV)基因表达的调控在很大程度上是由一些关键病毒蛋白相互协作并与细胞转录因子共同作用,在转录水平上进行控制的。然而,其中涉及的机制在很大程度上尚不清楚。为了确定对开放阅读框(ORF)4转录调控重要的序列,ORF 4本身编码一种转录调节因子,因此对其启动子进行了突变分析。这些研究确定了一个位于-69至-59之间(相对于转录起始位点)的元件,该元件对于VZV反式激活因子IE62刺激以及VZV感染时启动子的活性至关重要。DNA-蛋白质相互作用研究表明,VZV诱导一种特定蛋白质复合物与该元件结合,该复合物包含普遍存在的转录因子USF。ORF 4是第二个VZV基因(除VZV ORF 29外),其中USF结合在基因表达中起关键作用。