期刊
EUROPEAN JOURNAL OF BIOCHEMISTRY
卷 268, 期 10, 页码 2773-2778出版社
BLACKWELL SCIENCE LTD
DOI: 10.1046/j.1432-1327.2001.02226.x
关键词
p53; p300; CBP; transactivation; degradation; acetylation; MDM2
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.
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