Dobner T, Horikoshi N, Rubenwolf S, Shenk T
Institut für Medizinische Mikrobiologie und Hygiene, Universität Regensburg, Germany.
Science. 1996 Jun 7;272(5267):1470-3. doi: 10.1126/science.272.5267.1470.
The adenovirus E4orf6 protein is shown here to interact with the cellular tumor suppressor protein p53 and to block p53-mediated transcriptional activation. The adenovirus protein inhibited the ability of p53 to bind to human TAFII31, a component of transcription factor IID (TFIID). Earlier work demonstrated that the interaction of p53 with TAFII31 involves a sequence near the NH2-terminus of p53, whereas the E4orf6-p53 interaction occurs within amino acids 318 to 360 of p53. Thus, the E4orf6 protein interacts at a site on p53 distinct from the domain that binds to TAFII31 but nevertheless inhibits the p53-TAFII31 interaction.
在此显示腺病毒E4orf6蛋白与细胞肿瘤抑制蛋白p53相互作用,并阻断p53介导的转录激活。腺病毒蛋白抑制了p53与人TAFII31(转录因子IID(TFIID)的一个组分)结合的能力。早期研究表明,p53与TAFII31的相互作用涉及p53 NH2末端附近的一个序列,而E4orf6与p53的相互作用发生在p53的318至360氨基酸之间。因此,E4orf6蛋白在p53上与结合TAFII31的结构域不同的位点相互作用,但仍抑制p53-TAFII31的相互作用。