New insights into the functions and regulation of the transcriptional corepressors SMRT and N-CoR

被引:35
|
作者
Stanya, Kristopher J. [1 ,2 ,3 ]
Kao, Hung-Ying [1 ,2 ]
机构
[1] Case Western Reserve Univ, Sch Med, Dept Biochem, Cleveland, OH 44106 USA
[2] Univ Hosp Cleveland, Res Inst, Cleveland, OH 44106 USA
[3] Harvard Univ, Sch Publ Hlth, Dept Genet & Complex Dis, Boston, MA 02215 USA
来源
CELL DIVISION | 2009年 / 4卷
关键词
NUCLEAR RECEPTOR COREPRESSOR; HISTONE DEACETYLASE ACTIVITY; RESISTANT BREAST-CANCER; B KINASE ALPHA; CELL-CYCLE; HORMONE-RECEPTORS; MEDIATED REPRESSION; SILENCING MEDIATOR; SIGNALING PATHWAYS; IN-VIVO;
D O I
10.1186/1747-1028-4-7
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Corepressors are large proteins that facilitate transcriptional repression through recruitment of histone-modifying enzymes. Two major corepressors, SMRT (silencing mediator for retinoid and thyroid hormone receptors) and N-CoR (nuclear receptor corepressor), have been shown to mediate repression associated with nuclear receptors and a myriad of other transcription factors. This review will focus on recent studies on these proteins, including newly discovered physiological roles of the corepressors, their modes of regulation, their roles in antiestrogen-resistant breast cancer and their functions during the cell cycle.
引用
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页数:8
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