Nakade Koji, Zheng Hong, Ganguli Gitali, Buchwalter Gilles, Gross Christian, Wasylyk Bohdan
Institut de Génétique et de Biologie Moléculaire et Cellulaire, CNRS/INSERM/ULP, 67404 Illkirch cedex, France.
Mol Cell Biol. 2004 Feb;24(3):1132-42. doi: 10.1128/MCB.24.3.1132-1142.2004.
The tumor suppressor function of p53 is linked to its ability to repress gene expression, but the mechanisms of specific gene repression are poorly understood. We report that wild-type p53 inhibits an effector of the Ras oncogene/mitogen-activated protein (MAP) kinase pathway, the transcription factor Net. Tumor-associated mutant p53s are less efficient inhibitors. p53 inhibits by preventing phosphorylation of Net by MAP kinases. Loss of p53 in vivo leads to increased Net phosphorylation in response to wound healing and UV irradiation of skin. Our results show that p53 can repress specific gene expression by inhibiting Net, a factor implicated in cell cycle entry.
p53的肿瘤抑制功能与其抑制基因表达的能力相关,但具体的基因抑制机制仍知之甚少。我们报告称,野生型p53可抑制Ras癌基因/丝裂原活化蛋白(MAP)激酶途径的效应分子——转录因子Net。与肿瘤相关的突变型p53作为抑制剂的效率较低。p53通过阻止MAP激酶对Net的磷酸化来发挥抑制作用。体内p53缺失会导致在皮肤伤口愈合和紫外线照射后Net磷酸化增加。我们的结果表明,p53可通过抑制Net来抑制特定基因表达,Net是一种与细胞周期进入有关的因子。