Zambetti G P, Bargonetti J, Walker K, Prives C, Levine A J
Department of Molecular Biology, Princeton University, New Jersey 08544.
Genes Dev. 1992 Jul;6(7):1143-52. doi: 10.1101/gad.6.7.1143.
It has been reported recently that the wild-type p53 gene product can positively regulate the expression of a test gene adjacent to the enhancer-promoter elements of the murine muscle-specific creatine kinase (MCK) gene. This discussion reports the identification of a wild-type p53 protein-specific DNA-binding element located within the p53-responsive region of the MCK enhancer-promoter element. This p53 protein/DNA-binding element has been defined by DNase I footprint analysis, which identified a 50-bp region. This 50-bp sequence was sufficient to confer wild-type p53 responsiveness on a heterologous minimal promoter. The mutant forms of p53 protein are much less capable of stimulating this DNA element. This study has identified the first example of a naturally occurring wild-type p53-specific DNA-binding element that is able to mediate positive regulation of a test gene. The results suggest a biological function in gene regulation for the wild-type p53 protein that is lost or altered in the mutant p53 proteins.
最近有报道称,野生型p53基因产物可正向调节与小鼠肌肉特异性肌酸激酶(MCK)基因的增强子-启动子元件相邻的一个测试基因的表达。本讨论报告了在MCK增强子-启动子元件的p53反应区域内鉴定出一个野生型p53蛋白特异性DNA结合元件。该p53蛋白/DNA结合元件已通过DNase I足迹分析确定,该分析鉴定出一个50 bp的区域。这个50 bp的序列足以赋予异源最小启动子野生型p53反应性。p53蛋白的突变形式刺激该DNA元件的能力要弱得多。本研究鉴定出了第一个能够介导测试基因正向调节的天然存在的野生型p53特异性DNA结合元件实例。结果表明野生型p53蛋白在基因调控中具有生物学功能,而该功能在突变型p53蛋白中丧失或改变。