Lang J C, Spandidos D A, Wilkie N M
EMBO J. 1984 Feb;3(2):389-95. doi: 10.1002/j.1460-2075.1984.tb01817.x.
An enhancer-type sequence has been identified in the promoter region for the herpes simplex virus type 1 (HSV-1) immediate early (IE) mRNA 3. The enhancer-type activity is host cell dependent, being greater in human cells and Syrian hamster cells (the usual host cell for in vitro propagation of HSV) than in Chinese hamster or mouse cells. Enhancer activity is stimulated up to 10-fold after superinfection by tsK, a temperature-sensitive mutant of HSV-1. The induction of enhancer activity is independent of de novo protein synthesis, showing that trans-activation is effected by a component of the virion. We propose that trans-regulation of IE mRNA 3 is mediated through an enhancer-type sequence, and that this provides one explanation for previously described regulation of HSV IE mRNAs by virion components.
在单纯疱疹病毒1型(HSV-1)立即早期(IE)mRNA 3的启动子区域中已鉴定出一种增强子样序列。该增强子样活性依赖于宿主细胞,在人细胞和叙利亚仓鼠细胞(HSV体外增殖的常用宿主细胞)中比在中国仓鼠或小鼠细胞中更强。在被HSV-1的温度敏感突变体tsK超感染后,增强子活性可被刺激高达10倍。增强子活性的诱导不依赖于从头合成蛋白质,表明反式激活是由病毒粒子的一种成分实现的。我们提出,IE mRNA 3的反式调节是通过增强子样序列介导的,这为先前描述的病毒粒子成分对HSV IE mRNA的调节提供了一种解释。