Department of Biochemical Science and Technology, College of Life Science, National Taiwan University, Taipei, Taiwan.
Nucleic Acids Res. 2010 Aug;38(14):4687-700. doi: 10.1093/nar/gkq243. Epub 2010 Apr 12.
Epstein-Barr virus (EBV) expresses two transcription factors, Rta and Zta, during the immediate-early stage of the lytic cycle. The two proteins often collaborate to activate the transcription of EBV lytic genes synergistically. This study demonstrates that Rta and Zta form a complex via an intermediary protein, MCAF1, on Zta response element (ZRE) in vitro. The interaction among these three proteins in P3HR1 cells is also verified via coimmunoprecipitation, CHIP analysis and confocal microscopy. The interaction between Rta and Zta in vitro depends on the region between amino acid 562 and 816 in MCAF1. In addition, overexpressing MCAF1 enhances and introducing MCAF1 siRNA into the cells markedly reduces the level of the synergistic activation in 293T cells. Moreover, the fact that the synergistic activation depends on ZRE but not on Rta response element (RRE) originates from the fact that Rta and Zta are capable of activating the BMRF1 promoter synergistically after an RRE but not ZREs in the promoter are mutated. The binding of Rta-MCAF1-Zta complex to ZRE but not RRE also explains why Rta and Zta do not use RRE to activate transcription synergistically. Importantly, this study elucidates the mechanism underlying synergistic activation, which is important to the lytic development of EBV.
EBV 病毒在裂解周期的即刻早期表达两种转录因子,Rta 和 Zta。这两种蛋白经常协同作用以协同激活 EBV 裂解基因的转录。本研究表明,Rta 和 Zta 在体外通过 Zta 反应元件 (ZRE) 上的中间蛋白 MCAF1 形成复合物。还通过共免疫沉淀、CHIP 分析和共聚焦显微镜验证了这三种蛋白在 P3HR1 细胞中的相互作用。Rta 和 Zta 之间的相互作用取决于 MCAF1 中氨基酸 562 和 816 之间的区域。此外,过表达 MCAF1 增强了 293T 细胞中的协同激活作用,而引入 MCAF1 siRNA 则显著降低了协同激活作用的水平。此外,协同激活作用取决于 ZRE 而不是 Rta 反应元件 (RRE) 的事实源于这样一个事实,即 Rta 和 Zta 在启动子中的 RRE 而不是 ZRE 突变后能够协同激活 BMRF1 启动子。Rta-MCAF1-Zta 复合物与 ZRE 的结合而不是 RRE 也解释了为什么 Rta 和 Zta 不能使用 RRE 协同激活转录。重要的是,本研究阐明了协同激活的机制,这对于 EBV 的裂解发展很重要。