Rikitake Y, Moran E
Cold Spring Harbor Laboratory, New York 11724.
Mol Cell Biol. 1992 Jun;12(6):2826-36. doi: 10.1128/mcb.12.6.2826-2836.1992.
One of the major E1A-associated cellular proteins is a 300-kDa product (p300) that binds to the N-terminal region of the E1A products. The p300 binding site is distinct from sequences involved in binding the retinoblastoma product and other E1A-associated cellular products such as p60-cyclin A and p107. p300 binding to E1A is linked genetically to the enhancer repression function of E1A and the other E1A-mediated gene-regulating functions as well as to the transforming functions of E1A. However, the biochemical properties of p300 have not yet been characterized. We report here that p300 has an intrinsic DNA-binding activity and shows a preferential affinity for specific DNA sequences. The sequences selectively bound by p300 are related to those of a series of enhancer elements that are recognized by NF-kappa B. The direct physical interaction of p300 with enhancer elements provides a biochemical basis for the genetic evidence linking the E1A-mediated enhancer repression function with the p300-binding activity of E1A.
主要的E1A相关细胞蛋白之一是一种300kDa的产物(p300),它与E1A产物的N端区域结合。p300结合位点与参与结合视网膜母细胞瘤产物以及其他E1A相关细胞产物(如p60-细胞周期蛋白A和p107)的序列不同。p300与E1A的结合在遗传学上与E1A的增强子抑制功能、其他E1A介导的基因调控功能以及E1A的转化功能相关。然而,p300的生化特性尚未得到表征。我们在此报告,p300具有内在的DNA结合活性,并对特定DNA序列表现出优先亲和力。p300选择性结合的序列与一系列被NF-κB识别的增强子元件的序列相关。p300与增强子元件的直接物理相互作用为将E1A介导的增强子抑制功能与E1A的p300结合活性联系起来的遗传学证据提供了生化基础。