Scolnick D M, Chehab N H, Stavridi E S, Lien M C, Caruso L, Moran E, Berger S L, Halazonetis T D
Department of Molecular Genetics, The Wistar Institute, University of Pennsylvania, Philadelphia 19104-4268, USA.
Cancer Res. 1997 Sep 1;57(17):3693-6.
The structurally related transcriptional coactivators p300 and CBP possess histone acetyltransferase activity and associate with P/CAF, which is also a histone acetyltransferase. CBP and p300 have properties of tumor suppressor proteins; their interaction with P/CAF is disrupted by the adenoviral E1A oncoprotein, and the genes encoding CBP and p300 are mutated in human cancer. We observed a physical interaction between the transactivation domain of the p53 tumor suppressor protein and CBP. Furthermore, CBP and P/CAF enhanced the ability of p53 to activate expression of the endogenous p21(cip1/waf1) gene, whereas E1A and dominant negative CBP mutants suppressed p53-dependent p21(cip1/waf1) expression. These studies link two tumor suppressor families and provide a framework for understanding the molecular mechanism by which p53 activates transcription.
结构相关的转录共激活因子p300和CBP具有组蛋白乙酰转移酶活性,并与同样作为组蛋白乙酰转移酶的P/CAF相互作用。CBP和p300具有肿瘤抑制蛋白的特性;腺病毒E1A癌蛋白会破坏它们与P/CAF的相互作用,并且在人类癌症中,编码CBP和p300的基因发生了突变。我们观察到p53肿瘤抑制蛋白的反式激活结构域与CBP之间存在物理相互作用。此外,CBP和P/CAF增强了p53激活内源性p21(cip1/waf1)基因表达的能力,而E1A和显性负性CBP突变体则抑制p53依赖的p21(cip1/waf1)表达。这些研究将两个肿瘤抑制家族联系起来,并为理解p53激活转录的分子机制提供了一个框架。