Zeng Y X, Somasundaram K, el-Deiry W S
Howard Hughes Medical Institute, Department of Medicine and Genetics, University of Pennsylvania School of Medicine, Philadelphia 19104, USA.
Nat Genet. 1997 Jan;15(1):78-82. doi: 10.1038/ng0197-78.
The 52-kD Activator Protein (AP2) is a DNA-binding transcription factor implicated in signalling terminal differentiation. Profound developmental abnormalities have been recently observed in AP2-null mice. The molecular events by which AP2 promotes differentiation or development are, however, unknown. Increased expression of the universal cell cycle inhibitor p21WAF1/CIP1 occurs in growth-arrested terminally differentiating cells. In a search for cellular factors that could activate p21 during phorbol ester (TPA)-induced differentiation, we identified AP2 as a regulator of p21 expression. Mutagenesis of an AP2 DNA-binding site within a p21 promoter-luciferase reporter inhibited its activation by either AP2 transfection or TPA stimulation. Endogenous p21 protein levels were elevated and DNA synthesis was inhibited in AP2 versus control vector-transfected cells. Overexpression of AP2 in HepG2 human hepatoblastoma and SW480 human colon adenocarcinoma cells inhibited cell division and stable colony formation. These results link the differentiation-associated factor AP2 to negative cell cycle and growth control, possibly through p21 activation.
52-kD激活蛋白(AP2)是一种与信号转导终末分化有关的DNA结合转录因子。最近在AP2基因敲除小鼠中观察到了严重的发育异常。然而,AP2促进分化或发育的分子机制尚不清楚。在生长停滞的终末分化细胞中,普遍存在的细胞周期抑制剂p21WAF1/CIP1的表达增加。在寻找佛波酯(TPA)诱导分化过程中能够激活p21的细胞因子时,我们确定AP2是p21表达的调节因子。p21启动子-荧光素酶报告基因内AP2 DNA结合位点的诱变抑制了其通过AP2转染或TPA刺激的激活。与对照载体转染细胞相比,AP2转染细胞中内源性p21蛋白水平升高,DNA合成受到抑制。在HepG2人肝癌细胞和SW480人结肠腺癌细胞中过表达AP2抑制细胞分裂和稳定集落形成。这些结果将与分化相关的因子AP2与负性细胞周期和生长控制联系起来,可能是通过激活p21实现的。