Kovesdi I, Reichel R, Nevins J R
Proc Natl Acad Sci U S A. 1987 Apr;84(8):2180-4. doi: 10.1073/pnas.84.8.2180.
A product of the adenovirus gene E1A is responsible for the stimulation of transcription from six viral promoters as well as at least two cellular promoters. We have detected a HeLa cell factor, termed E2 promoter binding factor (E2F), that appears to mediate the transcriptional stimulation of the viral E2 promoter. Competition experiments revealed that E2F did not recognize and bind to the E1B, E3, E4, or major late promoter sequences. Furthermore, three additional promoters stimulated by E1A, heat shock protein 70, beta-globin, and early simian virus 40, do not bind E2F. In contrast, the factor does recognize sequences in the E1A enhancer, and within the E1A enhancer are duplicated binding sites for E2F. Finally, a single E2F binding site from the E1A enhancer can confer increased transcription to a mouse beta-globin promoter, dependent on the action of the E1A gene product. This stimulation requires binding of E2F since methylation of the binding site, which blocks binding in vitro, reduces transcription stimulation in vivo. We, therefore, conclude that E2F is likely to be responsible for the E1A-mediated stimulation of the E1A gene as well as the E2 gene but is not involved in the activation of the other E1A-inducible promoters.
腺病毒基因E1A的一种产物负责刺激六个病毒启动子以及至少两个细胞启动子的转录。我们检测到一种名为E2启动子结合因子(E2F)的HeLa细胞因子,它似乎介导了病毒E2启动子的转录刺激。竞争实验表明,E2F不识别并结合E1B、E3、E4或主要晚期启动子序列。此外,E1A刺激的另外三个启动子,即热休克蛋白70、β-珠蛋白和猿猴病毒40早期启动子,不结合E2F。相反,该因子确实识别E1A增强子中的序列,并且在E1A增强子内有E2F的重复结合位点。最后,来自E1A增强子的单个E2F结合位点可以使小鼠β-珠蛋白启动子的转录增加,这依赖于E1A基因产物的作用。这种刺激需要E2F的结合,因为结合位点的甲基化在体外会阻止结合,在体内会降低转录刺激。因此,我们得出结论,E2F可能负责E1A介导的E1A基因以及E2基因的刺激,但不参与其他E1A诱导型启动子的激活。