Zeng X, Lee H, Zhang Q, Lu H
Department of Biochemistry and Molecular Biology, Oregon Health Science University, Portland, Oregon 97201, USA.
J Biol Chem. 2001 Jan 5;276(1):48-52. doi: 10.1074/jbc.C000722200.
We previously reported that p73, like p53, utilizes p300 or cAMP-response element-binding protein-binding protein as its coactivator. Here, we extended this work by further examining whether the intrinsic acetylase activity of p300 is necessary for stimulating p73 function. Although p300 acetylated the C-terminal fragment of p73 (amino acids 311-636) in vitro, it was unable to efficiently acetylate the full-length p73. Consistently, p300 did not acetylate p73 in vivo when both the proteins were overexpressed in cells. Also, an acetylase-defective mutant p300 named p300AT2 was able to elevate p73-dependent transcription in cells. p300 associated with p73 when forming DNA-protein complexes and stabilized p73 proteins. These results demonstrate that p300 does not need its acetylase activity to be a coactivator of p73.
我们之前报道过,p73与p53一样,利用p300或环磷酸腺苷反应元件结合蛋白结合蛋白作为其共激活因子。在此,我们通过进一步研究p300的内在乙酰转移酶活性对于刺激p73功能是否必要来扩展这项工作。虽然p300在体外可使p73的C末端片段(氨基酸311 - 636)乙酰化,但它无法有效使全长p73乙酰化。同样,当这两种蛋白在细胞中过表达时,p300在体内也不能使p73乙酰化。此外,一种名为p300AT2的乙酰转移酶缺陷型突变体p300能够提高细胞中p73依赖的转录水平。p300在形成DNA - 蛋白质复合物时与p73结合,并稳定p73蛋白。这些结果表明,p300作为p73的共激活因子并不需要其乙酰转移酶活性。