Sharp, an inducible cofactor that integrates nuclear receptor repression and activation

被引:260
作者
Shi, YH [1 ]
Downes, M [1 ]
Xie, W [1 ]
Kao, HY [1 ]
Ordentlich, P [1 ]
Tsai, CC [1 ]
Hon, M [1 ]
Evans, RM [1 ]
机构
[1] Salk Inst Biol Studies, Howard Hughes Med Inst, Gene Express Lab, La Jolla, CA 92037 USA
关键词
SMRT; HDAC1; SRA; attenuation of hormonal response;
D O I
10.1101/gad.871201
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A yeast two-hybrid screen using the conserved carboxyl terminus of the nuclear receptor corepressor SMRT as a bait led to the isolation of a novel human gene termed SHARP (SMRT/HDAC1 Associated Repressor Protein). SHARP is a potent transcriptional repressor whose repression domain (RD) interacts directly with SMRT and at least five members of the NuRD complex including HDAC1 and HDAC2. In addition, SHARP binds to the steroid receptor RNA coactivator SRA via an intrinsic RNA binding domain and suppresses SRA-potentiated steroid receptor transcription activity. Accordingly, SHARP has the capacity to modulate both liganded and nonliganded nuclear receptors. Surprisingly, the expression of SHARP is itself steroid inducible, suggesting a simple feedback mechanism for attenuation of the hormonal response.
引用
收藏
页码:1140 / 1151
页数:12
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