Fåhraeus R, Jansson A, Ricksten A, Sjöblom A, Rymo L
Department of Tumor Biology, Karolinska Institute, Stockholm, Sweden.
Proc Natl Acad Sci U S A. 1990 Oct;87(19):7390-4. doi: 10.1073/pnas.87.19.7390.
Previous studies suggest that the Epstein-Barr virus nuclear antigen EBNA2 participates in the regulation of the expression of the viral latent membrane protein (LMP). We have used reporter plasmids containing DNA fragments of the 5' flanking region of the LMP gene in cotransfection experiments to analyze the effect of EBNA2 on the activity of the LMP promoter. The results show that the LMP promoter is controlled by positive and negative transcription elements in a DNA fragment that contains the LMP transcription initiation site and 634 base pairs of upstream sequences. The promoter is activated by EBNA2. The region between position -54 and +40 relative to the mRNA cap site contains a positive transcription element that is constitutively active in DG75 cells and independent of EBNA2. The -106 to -54 region contains a negative regulatory element that prevents adjacent positive elements from functioning in the absence of EBNA2. Regulatory sequences between -324 and -144 participate in maintaining a high level of transcription of the LMP promoter after induction with EBNA2. The regulatory elements in the -634 to -54 promoter region have the characteristics of an inducible enhancer, including orientation independence and ability to regulate a heterologous promoter.
以往的研究表明,爱泼斯坦 - 巴尔病毒核抗原EBNA2参与病毒潜伏膜蛋白(LMP)表达的调控。我们在共转染实验中使用了含有LMP基因5'侧翼区DNA片段的报告质粒,以分析EBNA2对LMP启动子活性的影响。结果表明,LMP启动子受一个DNA片段中的正负转录元件控制,该片段包含LMP转录起始位点和634个碱基对的上游序列。该启动子被EBNA2激活。相对于mRNA帽位点,-54至+40位置之间的区域包含一个正转录元件,它在DG75细胞中具有组成性活性且不依赖于EBNA2。-106至-54区域包含一个负调控元件,在没有EBNA2的情况下,它会阻止相邻的正元件发挥作用。-324至-144之间的调控序列参与维持EBNA2诱导后LMP启动子的高水平转录。-634至-54启动子区域中的调控元件具有可诱导增强子的特征,包括方向独立性和调控异源启动子的能力。