Oliner J D, Pietenpol J A, Thiagalingam S, Gyuris J, Kinzler K W, Vogelstein B
Johns Hopkins Oncology Centre, Baltimore, Maryland 21231.
Nature. 1993 Apr 29;362(6423):857-60. doi: 10.1038/362857a0.
The tumour-suppressor gene p53 is inactivated in most human malignancies either by missense mutations or by binding to oncogenic proteins. In human soft tissue sarcomas, inactivation apparently results from MDM2 gene amplification. MDM2 is an oncogene product that may function by binding to p53 and inhibiting its ability to activate transcription. Here we show that, when expressed in Saccharomyces cerevisiae, human MDM2 inhibits human p53's ability to stimulate transcription by binding to a region that nearly coincides with the p53 acidic activation domain. The isolated p53 activation domain fused to another DNA-binding protein is also inactivated by MDM2, confirming that MDM2 can inhibit p53 function by concealing the activation domain of p53 from the cellular transcription machinery.
肿瘤抑制基因p53在大多数人类恶性肿瘤中因错义突变或与致癌蛋白结合而失活。在人类软组织肉瘤中,失活显然是由MDM2基因扩增导致的。MDM2是一种癌基因产物,可能通过与p53结合并抑制其激活转录的能力来发挥作用。我们在此表明,当在酿酒酵母中表达时,人类MDM2通过与一个几乎与p53酸性激活域重合的区域结合,抑制人类p53刺激转录的能力。与另一种DNA结合蛋白融合的分离出的p53激活域也被MDM2失活,这证实MDM2可通过向细胞转录机制隐藏p53的激活域来抑制p53功能。