Chatton B, Bocco J L, Gaire M, Hauss C, Reimund B, Goetz J, Kedinger C
Laboratoire de Génétique Moléculaire des Eucaryotes, Unité 184 de Biologie Moléculaire et de Génie Génétique, Institut National de la Santé et de la Recherche Médicale, Strasbourg, France.
Mol Cell Biol. 1993 Jan;13(1):561-70. doi: 10.1128/mcb.13.1.561-570.1993.
We recently isolated three cDNA clones encoding closely related proteins (ATFa1, ATFa2, and ATFa3) that belong to the activating transcription factor-cyclic AMP-responsive element family of cellular transcription factors. Using cotransfection experiments, we showed that these proteins mediate the transcriptional activation induced by the adenovirus E1a 13S mRNA gene product and that the zinc-binding domains present in both E1a conserved region 3 and the most N-terminal portion of the ATFa proteins play crucial roles in this activity. Reciprocal coimmunoprecipitation experiments demonstrated direct interactions between these proteins. Neither the conserved region 3 domain of E1a nor the N-terminal metal-binding element of ATFa is essential for these interactions. The simultaneous alteration of both the N-terminal and the C-terminal domains of ATFa abolished E1a binding, while either mutation alone failed to impair these interactions.
我们最近分离出了三个编码密切相关蛋白质(ATFa1、ATFa2和ATFa3)的cDNA克隆,这些蛋白质属于细胞转录因子中的激活转录因子-环磷酸腺苷反应元件家族。通过共转染实验,我们表明这些蛋白质介导了腺病毒E1a 13S mRNA基因产物诱导的转录激活,并且E1a保守区域3和ATFa蛋白质最N端部分中存在的锌结合结构域在该活性中起关键作用。相互的共免疫沉淀实验证明了这些蛋白质之间的直接相互作用。E1a的保守区域3结构域和ATFa的N端金属结合元件对于这些相互作用都不是必需的。ATFa的N端和C端结构域同时改变会消除E1a结合,而单独任何一个突变都不会损害这些相互作用。