死亡相关蛋白6
雄激素受体
相扑蛋白
LNCaP公司
生物
交易激励
心理压抑
前列腺癌
细胞生物学
癌症研究
转录因子
分子生物学
核蛋白
基因表达
泛素
遗传学
癌症
基因
作者
Ding-Yen Lin,Hsin-I Fang,Ai-Hong Ma,Yen‐Sung Huang,Yeong‐Shiau Pu,Guido Jenster,Hsing-Jien Kung,Hsiu-Ming Shih
标识
DOI:10.1128/mcb.24.24.10529-10541.2004
摘要
The transcriptional activity of the androgen receptor (AR) modulated by positive or negative regulators plays a critical role in controlling the growth and survival of prostate cancer cells. Although numerous positive regulators have been identified, negative regulators of AR are less well understood. We report here that Daxx functions as a negative AR coregulator through direct protein-protein interactions. Overexpression of Daxx suppressed AR-mediated promoter activity in COS-1 and LNCaP cells and AR-mediated prostate-specific antigen expression in LNCaP cells. Conversely, downregulation of endogenous Daxx expression by RNA interference enhances androgen-induced prostate-specific antigen expression in LNCaP cells. In vitro and in vivo interaction studies revealed that Daxx binds to both the amino-terminal and the DNA-binding domain of the AR. Daxx proteins interfere with the AR DNA-binding activity both in vitro and in vivo. Moreover, sumoylation of AR at its amino-terminal domain is involved in Daxx interaction and trans-repression. Together, these findings not only provide a novel role of Daxx in controlling AR transactivation activity but also uncover the mechanism underlying sumoylation-dependent transcriptional repression of the AR.
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