共 50 条
p300/CBP/p53 interaction and regulation of the p53 response
被引:203
作者:

Grossman, SR
论文数: 0 引用数: 0
h-index: 0
机构: Dana Farber Canc Inst, Dept Adult Oncol, Boston, MA 02115 USA
机构:
[1] Dana Farber Canc Inst, Dept Adult Oncol, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Dept Canc Biol, Boston, MA 02115 USA
[3] Brigham & Womens Hosp, Dept Med, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Boston, MA USA
来源:
EUROPEAN JOURNAL OF BIOCHEMISTRY
|
2001年
/
268卷
/
10期
关键词:
p53;
p300;
CBP;
transactivation;
degradation;
acetylation;
MDM2;
D O I:
10.1046/j.1432-1327.2001.02226.x
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:
Substantial evidence points to a critical role for the p300/CREB binding protein (CBP) coactivators in p53 responses to DNA damage. p300/CBP and the associated protein P/CAF bind to and acetylate p53 during the DNA damage response, and are needed for full p53 transactivation as well as downstream p53 effects of growth arrest and/or apoptosis. Beyond this simplistic model, p300/CBP appear to be complex integrators of signals that regulate p53, and biochemically, the multipartite p53/p300/CBP interaction is equally complex. Through physical interaction with p53, p300/CBP can both positively and negatively regulate p53 transactivation, as well as p53 protein turnover depending on cellular context and environmental stimuli, such as DNA damage.
引用
收藏
页码:2773 / 2778
页数:6
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