Yew P R, Liu X, Berk A J
Department of Microbiology and Molecular Genetics, University of California, Los Angeles 90024-1570.
Genes Dev. 1994 Jan;8(2):190-202. doi: 10.1101/gad.8.2.190.
Many DNA tumor viruses express a protein that inhibits transcriptional activation by the tumor-suppressing transcription factor p53. We report that adenovirus E1B 55K represses p53-mediated activation by a mechanism not described previously. E1B 55K binds p53 without displacing it from its DNA-binding site. A fusion of E1B 55K to the GAL4 DNA-binding domain represses transcription from a variety of promoters with engineered upstream GAL4-binding sites. Mutations within E1B 55K that interfere with its transforming activity and its ability to inhibit p53-mediated trans-activation also interfere with transcriptional repression by the GAL4-55K fusion. These results demonstrate that E1B 55K functions as a direct transcriptional repressor that is targeted to p53-responsive genes by binding to p53.
许多DNA肿瘤病毒表达一种能抑制肿瘤抑制转录因子p53介导的转录激活的蛋白质。我们报告称,腺病毒E1B 55K通过一种此前未被描述的机制抑制p53介导的激活。E1B 55K与p53结合,但不会将其从DNA结合位点上置换下来。E1B 55K与GAL4 DNA结合域的融合蛋白可抑制来自各种具有工程化上游GAL4结合位点的启动子的转录。E1B 55K内干扰其转化活性及其抑制p53介导的反式激活能力的突变,也会干扰GAL4 - 55K融合蛋白的转录抑制作用。这些结果表明,E1B 55K作为一种直接的转录抑制因子,通过与p53结合靶向p53反应基因发挥作用。