Modes of p53 Regulation

被引:1376
作者
Kruse, Jan-Philipp [1 ,2 ]
Gu, Wei [1 ,2 ]
机构
[1] Columbia Univ, Coll Phys & Surg, Inst Canc Genet, New York, NY 10032 USA
[2] Columbia Univ, Coll Phys & Surg, Dept Pathol & Cell Biol, New York, NY 10032 USA
关键词
DNA-BINDING DOMAIN; UBIQUITIN LIGASE ACTIVITY; TUMOR-SUPPRESSOR P53; SMALL-MOLECULE INHIBITORS; RIBOSOMAL-PROTEIN L11; ACTIVITY IN-VIVO; EMBRYONIC LETHALITY; ACTIVATES P53; NEGATIVE REGULATOR; POSTTRANSLATIONAL MODIFICATIONS;
D O I
10.1016/j.cell.2009.04.050
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The traditional view of p53 activation includes three steps-p53 stabilization, DNA binding, and transcriptional activation. However, recent studies indicate that each step of p53 activation is more complex than originally anticipated. Moreover, both genetic studies in mice and in vitro studies with purified components suggest that the classical model may not be sufficient to explain all aspects of p53 activation in vivo. To reconcile these differences, we propose that antirepression, the release of p53 from repression by factors such as Mdm2 and MdmX, is a key step in the physiological activation of p53.
引用
收藏
页码:609 / 622
页数:14
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