Proteasomal regulation of nuclear receptor corepressor-mediated repression

被引:184
作者
Zhang, JS
Guenther, MG
Carthew, RW
Lazar, MA [1 ]
机构
[1] Univ Penn, Sch Med, Dept Med, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Dept Genet, Philadelphia, PA 19104 USA
[3] Univ Penn, Sch Med, Dept Biochem, Philadelphia, PA 19104 USA
[4] Univ Pittsburgh, Dept Biol Sci, Pittsburgh, PA 15260 USA
关键词
nuclear receptor corepressor; proteasomal regulation; repression; RevErb; thyroid hormone receptor; cell specificity;
D O I
10.1101/gad.12.12.1775
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Repression of gene transcription is a fundamental property of nuclear hormone receptors. We report here that cell-specific repression by nuclear receptors correlates with levels of nuclear receptor corepressor (N-CoR) protein. N-CoR protein levels are regulated by mSiah2, a mammalian homolog of Drosophila Seven in absentia that targets N-CoR for proteasomal degradation. mSiah2 expression is cell-type specific and differentially regulates the repressive activities of nuclear receptors. These findings establish targeted proteolysis of transcriptional coregulators as a mechanism for cell-specific regulation of gene transcription.
引用
收藏
页码:1775 / 1780
页数:6
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