p53 ubiquitination by Mdm2: A never ending tail?

被引:72
作者
Coutts, Amanda S. [1 ]
Adams, Cassandra J. [1 ]
La Thangue, Nicholas B. [1 ]
机构
[1] Univ Oxford, Div Med Sci, Dept Clin Pharmacol, Oxford OX3 7DQ, England
关键词
p53; Ubiquitin; Mdm2; DNA damage; ATM-DEPENDENT PHOSPHORYLATION; SUPPRESSOR PROTEIN P53; RING-FINGER DOMAIN; DNA-BINDING DOMAIN; TUMOR-SUPPRESSOR; LIGASE ACTIVITY; NUCLEAR EXPORT; IN-VITRO; MDM2-DEPENDENT UBIQUITINATION; PROMOTES UBIQUITINATION;
D O I
10.1016/j.dnarep.2009.01.008
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学];
摘要
p53 function is of critical importance in suppressing human cancer formation, highlighted by the fact that the majority of human tumors harbor compromised p53 activity. In normal cells, p53 is held at low levels in a latent form and cellular stress results in the rapid stabilization of p53. Mdm2 mediates ubiquitin-dependent degradation of p53 which plays a key role in maintaining cellular p53 levels. Ubiquitination was. until recently, considered a straightforward system involved in p53 degradation, but recent work has demonstrated how ubiquitination can alter p53 activity, not stability. in this review we summarize cut-rent understanding on p53 ubiquitination by Mdm2 with a particular focus on how the balance between protein levels and other post-translational modifications will direct the p53 response. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:483 / 490
页数:8
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