Flemington E, Speck S H
Division of Tumor Virology, Dana-Farber Cancer Institute, Boston, Massachusetts.
J Virol. 1990 Mar;64(3):1217-26. doi: 10.1128/JVI.64.3.1217-1226.1990.
The product of the Epstein-Barr virus BZLF1 gene encodes a protein which is related to c-fos, it has been shown to bind specifically to a consensus AP-1 site, and its expression in latently Epstein-Barr virus-infected lymphocytes is sufficient to trigger the viral lytic cycle. We identified several elements within the BZLF1 promoter (Zp) which are responsive to the phorbol ester 12-O-tetradecanoylphorbol-13-acetate (TPA), an inducer of the viral lytic cycle. These elements fall into two classes based on the factors which bind to these sequences and their resulting functional behavior. Four of the elements are homologous (ZI elements) and share homology to a protein-binding domain in the promoter region of the coordinately expressed BRLF1 gene. When cloned upstream of heterologous promoters, the ZI elements function as silencers which exhibit TPA-inducible enhancer activity. A distinct TPA-responsive element (ZII) is located near the TATA box and shares homology with the AP-1-binding site in the c-jun promoter. A synthetic oligonucleotide with a sequence corresponding to the ZII element effectively competes for binding of nuclear factors to the c-jun AP-1 site. Furthermore, we found that a complex of c-jun and c-fos bound to the ZII domain.
爱泼斯坦-巴尔病毒BZLF1基因的产物编码一种与c-fos相关的蛋白质,已证明它能特异性结合共有AP-1位点,并且其在潜伏感染爱泼斯坦-巴尔病毒的淋巴细胞中的表达足以触发病毒的裂解周期。我们在BZLF1启动子(Zp)中鉴定出几个对佛波酯12-O-十四酰佛波醇-13-乙酸酯(TPA)有反应的元件,TPA是病毒裂解周期的诱导剂。根据与这些序列结合的因子及其产生的功能行为,这些元件可分为两类。其中四个元件是同源的(ZI元件),与协同表达的BRLF1基因启动子区域中的一个蛋白质结合结构域具有同源性。当克隆到异源启动子上游时,ZI元件作为沉默子发挥作用,表现出TPA诱导的增强子活性。一个独特的TPA反应元件(ZII)位于TATA框附近,与c-jun启动子中的AP-1结合位点具有同源性。一个与ZII元件序列对应的合成寡核苷酸能有效竞争核因子与c-jun AP-1位点的结合。此外,我们发现c-jun和c-fos的复合物与ZII结构域结合。