Recruitment of p300/CBP in p53-dependent signal pathways

被引:606
|
作者
Avantaggiati, ML
Ogryzko, V
Gardner, K
Giordano, A
Levine, AS
Kelly, K
机构
[1] NCI,PATHOL LAB,BETHESDA,MD 20892
[2] NICHHD,LAB MOL GROWTH REGULAT,NIH,BETHESDA,MD 20892
[3] NICHHD,SECT DNA REPLICAT REPAIR & MUTAGENESIS,NIH,BETHESDA,MD 20892
[4] THOMAS JEFFERSON UNIV,SBARRO INST CANC RES & MOL MED,PHILADELPHIA,PA 19107
关键词
D O I
10.1016/S0092-8674(00)80304-9
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 products of the p53 and CBP/p300 genes have been individually implicated in control of cell growth and regulation of transcription. p53 is known to act as a positive and negative regulator of gene expression. Here we show that p53, in both wild-type and mutant conformation, forms a specific protein complex with p300. However, in its wild-type but not mutant conformation, p53 inhibits a promoter containing the DNA-binding sequences for the transcription factor AP1, in a p300-dependent manner. p300 stimulates the transcriptional activity of p53 on p53-regulated promoters, and it enhances the responsiveness to a physiological upstream modulator of p53 function, ionizing radiation. A dominant negative form of p300 prevents transcriptional activation by p53, and it counteracts p53-mediated G1 arrest and apoptosis. The data implicate p300 as an important component of p53-signaling, thus providing new insight into the mechanisms of cellular proliferation.
引用
收藏
页码:1175 / 1184
页数:10
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