Fu M, Wang C, Reutens A T, Wang J, Angeletti R H, Siconolfi-Baez L, Ogryzko V, Avantaggiati M L, Pestell R G
Albert Einstein Cancer Center, Department of Developmental and Molecular Biology, Albert Einstein College of Medicine, Bronx, New York 10461, USA.
J Biol Chem. 2000 Jul 7;275(27):20853-60. doi: 10.1074/jbc.M000660200.
The androgen receptor (AR) is a sequence-specific DNA-binding protein that plays a key role in prostate cancer cellular proliferation by dihydrotestosterone and the induction of secondary sexual characteristics. In this study we demonstrate that the AR can be modified by acetylation in vitro and in vivo. p300 and p300/cAMP-response element-binding protein acetylated the AR at a highly conserved lysine-rich motif carboxyl-terminal to the zinc finger DNA-binding domain. [(14)C]acetate-labeling experiments demonstrated that AR acetylation by p300 in cultured cells requires the same residues identified in vitro. Point mutation of the AR acetylation site (K632A/K633A) abrogated dihydrotestosterone-dependent transactivation of the AR in cultured cells. Mutation of the p300 CH3 region or the p300/cAMP-response element-binding protein histone acetylase domain reduced ligand-dependent AR function. The identification of the AR as a direct target of histone acetyltransferase co-activators has important implications for targeting inhibitors of AR function.
雄激素受体(AR)是一种序列特异性DNA结合蛋白,通过二氢睾酮在前列腺癌细胞增殖以及诱导第二性征方面发挥关键作用。在本研究中,我们证明AR在体外和体内均可被乙酰化修饰。p300和p300/环磷酸腺苷反应元件结合蛋白在锌指DNA结合结构域羧基末端高度保守的富含赖氨酸基序处使AR发生乙酰化。[¹⁴C]乙酸盐标记实验表明,培养细胞中p300介导的AR乙酰化需要与体外鉴定相同的残基。AR乙酰化位点(K632A/K633A)的点突变消除了培养细胞中AR的二氢睾酮依赖性反式激活。p300 CH3区域或p300/环磷酸腺苷反应元件结合蛋白组蛋白乙酰转移酶结构域的突变降低了配体依赖性AR功能。将AR鉴定为组蛋白乙酰转移酶共激活因子的直接靶点对于靶向AR功能抑制剂具有重要意义。