Angel P, Imagawa M, Chiu R, Stein B, Imbra R J, Rahmsdorf H J, Jonat C, Herrlich P, Karin M
Cell. 1987 Jun 19;49(6):729-39. doi: 10.1016/0092-8674(87)90611-8.
The promoter regions of several phorbol diester-(TPA-) inducible genes (collagenase, stromelysin, hMT IIA, and SV40) share a conserved 9 bp motif. Synthetic copies of these closely related sequences conferred TPA inducibility upon heterologous promoters. Footprinting analysis indicated that these TPA-responsive elements (TREs) are recognized by a common cellular protein: the previously described transcription factor AP-1. A point mutation that eliminated the basal and induced activity of the TRE also interfered with its ability to bind AP-1. Treatment of cultured cells with TPA led to a rapid 3- to 4-fold increase in TRE binding activity, by a posttranslational mechanism. These results strongly suggest that AP-1 is at the receiving end of a complex pathway responsible for transmitting the effects of phorbol ester tumor promoters from the plasma membrane to the transcriptional machinery.
几种佛波酯(TPA)诱导型基因(胶原酶、基质溶解素、hMT IIA和SV40)的启动子区域共享一个保守的9碱基基序。这些密切相关序列的合成拷贝赋予异源启动子TPA诱导性。足迹分析表明,这些TPA反应元件(TREs)被一种常见的细胞蛋白识别:先前描述的转录因子AP-1。消除TRE基础活性和诱导活性的点突变也会干扰其与AP-1结合的能力。用TPA处理培养细胞会通过翻译后机制使TRE结合活性迅速增加3至4倍。这些结果强烈表明,AP-1处于负责将佛波酯肿瘤启动子的作用从质膜传递到转录机制的复杂信号通路的接收端。