Magnaldo T, Bernerd F, Freedberg I M, Ohtsuki M, Blumenberg M
Ronald O. Perelman Department of Dermatology, NYU Medical Center, New York 10016.
DNA Cell Biol. 1993 Dec;12(10):911-23. doi: 10.1089/dna.1993.12.911.
In most malignant and benign skin diseases, the normal pattern of keratin expression is altered. Among other phenotypic changes, the expression of hyperproliferation- and activation-associated keratins K#16 and K#6 is induced. Because the molecular mechanisms and the nuclear regulators involved in this induction are unknown, we have characterized the transcriptional regulators of expression of the keratin K#16 promoter. Our previous studies have shown that the transcription of K#16 is strongly and specifically induced in epidermal keratinocytes by epidermal growth factor (EGF), through the EGF-responsive element (RE). In the present work, using an electrophoretic mobility-shift assay, we have found several nuclear protein binding sites that have been identified as an Sp1 site, an AP2 site, the EGF-RE, and an enhancer element. The function of each site was assessed in transfection assays using specific deletions. Both the Sp1 and EGF-RE sites are essential for K#16 promoter activity. The site that functions as an independent enhancer, E, was found adjacent to and interacting with a sequence recognized by the AP2 transcription factor. This knowledge of the nuclear regulators of expression of the disease-associated K#16 keratin provides insight into the molecular parameters that might be important in skin diseases.
在大多数恶性和良性皮肤病中,角蛋白的正常表达模式会发生改变。在其他表型变化中,与过度增殖和激活相关的角蛋白K16和K6的表达会被诱导。由于参与这种诱导的分子机制和核调节因子尚不清楚,我们对角蛋白K16启动子表达的转录调节因子进行了表征。我们之前的研究表明,表皮生长因子(EGF)通过EGF反应元件(RE)在表皮角质形成细胞中强烈且特异性地诱导K16的转录。在本研究中,我们使用电泳迁移率变动分析,发现了几个核蛋白结合位点,它们分别被鉴定为一个Sp1位点、一个AP2位点、EGF-RE和一个增强子元件。通过使用特定缺失的转染实验评估了每个位点的功能。Sp1和EGF-RE位点对于K16启动子活性都是必不可少的。发现作为独立增强子起作用的位点E与AP2转录因子识别的序列相邻并相互作用。对与疾病相关的K16角蛋白表达的核调节因子的这种了解,为深入了解在皮肤病中可能重要的分子参数提供了依据。