Daxx mediates the small ubiquitin-like modifier-dependent transcriptional repression of Smad

被引:98
作者
Chang, CC
Lin, DY
Fang, HI
Chen, RH
Shih, HM
机构
[1] Natl Taiwan Univ, Coll Med, Inst Mol Med, Taipei 11529, Taiwan
[2] Natl Taiwan Univ, Coll Med, Grad Inst Life Sci, Natl Def Med Ctr, Taipei 11529, Taiwan
[3] Natl Taiwan Univ, Coll Med, Div Mol & Genom Med, Natl Hlth Res Inst, Taipei 11529, Taiwan
关键词
D O I
10.1074/jbc.M409161200
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
Daxx has been shown to function as an apoptosis regulator and transcriptional repressor via its interaction with various cytoplasmic and nuclear proteins. Here, we showed that Daxx interacts with Smad4 and represses its transcriptional activity via the C-terminal domain of Daxx. In vitro and in vivo interaction studies indicated that the binding of Smad4 to Daxx depends on Smad4 sumoylation. Substitution of Smad4 SUMO conjugation residue lysine 159, but not 113, to arginine not only disrupted Smad4-Daxx interaction but also relieved Daxx-elicited repression of Smad4 transcriptional activity. Furthermore, chromatin immunoprecipitation analyses revealed the recruitment of Daxx to an endogenous, Smad4-targeted promoter in a Lys(159) sumoylation-dependent manner. Finally, down-regulation of Daxx expression by RNA interference enhanced transforming growth factor beta-induced transcription of reporter and endogenous genes through a Smad4-dependent, but not K159R-Smad4-dependent, manner. Together, these results indicate that Daxx suppresses Smad4-mediated transcriptional activity by direct interaction with the sumoylated Smad4 and identify a novel role of Daxx in regulating transforming growth factor beta signaling.
引用
收藏
页码:10164 / 10173
页数:10
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