Shiio Y, Yamamoto T, Yamaguchi N
Department of Virology, University of Tokyo, Japan.
Proc Natl Acad Sci U S A. 1992 Jun 15;89(12):5206-10. doi: 10.1073/pnas.89.12.5206.
Mutation of the p53 gene is one of the most frequent genetic changes found in human cancers. Recent experiments indicated that p53 might contain a transcription-activating domain, which functions when directed to a promoter. This study shows that wild-type p53 suppresses transcription of the retinoblastoma (Rb) gene. From deletion and mutagenesis experiments, a cis-acting element (GGAAGTGA) susceptible to regulation by p53 was mapped within the Rb promoter. This element overlaps the basal transcription unit of the Rb promoter, suggesting that p53 suppresses Rb transcription through inhibition of the basal promoter activity. The N-terminal acidic and C-terminal basic domains of p53 were both required for this suppression. These findings indicate that p53 can act as a transcriptional regulator in vivo.
p53基因的突变是在人类癌症中发现的最常见的基因变化之一。最近的实验表明,p53可能包含一个转录激活结构域,当它被导向一个启动子时发挥作用。这项研究表明,野生型p53抑制视网膜母细胞瘤(Rb)基因的转录。通过缺失和诱变实验,在Rb启动子内定位了一个易受p53调控的顺式作用元件(GGAAGTGA)。该元件与Rb启动子的基础转录单元重叠,这表明p53通过抑制基础启动子活性来抑制Rb转录。p53的N端酸性结构域和C端碱性结构域对于这种抑制都是必需的。这些发现表明p53在体内可作为一种转录调节因子。