Negative modulation of androgen receptor transcriptional activity by Daxx

被引:91
|
作者
Lin, DY
Fang, HI
Ma, AH
Huang, YS
Pu, YS
Jenster, G
Kung, HJ
Shih, HM
机构
[1] Natl Hlth Res Inst, Div Mol & Genom Med, Taipei 11529, Taiwan
[2] Natl Def Med Ctr, Grad Inst Life Sci, Taipei, Taiwan
[3] Natl Taiwan Univ, Dept Urol, Coll Med, Taipei, Taiwan
[4] Univ Calif Davis, Ctr Canc, Sacramento, CA 95817 USA
[5] Josephine Nefkens Inst, Erasmus Med Ctr, Dept Urol, Rotterdam, Netherlands
关键词
D O I
10.1128/MCB.24.24.10529-10541.2004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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.
引用
收藏
页码:10529 / 10541
页数:13
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