Controlling nuclear receptors: The circular logic of cofactor cycles

被引:378
作者
Perissi, V [1 ]
Rosenfeld, MG [1 ]
机构
[1] Univ Calif San Diego, Howard Hughes Med Inst, Dept Med, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nrm1680
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Nuclear receptors regulate many biologically important processes in development and homeostasis by their bimodal function as repressors and activators of gene transcription. A finely tuned modulation of the transcriptional activities of nuclear receptors is crucial for determining highly specific and diversified programmes of gene expression. Recent studies have provided insights into the molecular mechanisms that are required to switch between repression and activation functions, the combinatorial roles of the multiple cofactor complexes that are required for mediating transcriptional regulation, and the central question of how several different signalling pathways can be integrated at the nuclear level to achieve specific profiles of gene expression.
引用
收藏
页码:542 / 554
页数:13
相关论文
共 159 条
[61]   Translating the histone code [J].
Jenuwein, T ;
Allis, CD .
SCIENCE, 2001, 293 (5532) :1074-1080
[62]   SMRT and N-CoR corepressors are regulated by distinct kinase signaling pathways [J].
Jonas, BA ;
Privalsky, ML .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (52) :54676-54686
[63]  
Jones PL, 2003, CURR TOP MICROBIOL, V274, P237
[64]   Transcriptional specificity of human SWI/SNF BRG1 and BRM chromatin remodeling complexes [J].
Kadam, S ;
Emerson, BM .
MOLECULAR CELL, 2003, 11 (02) :377-389
[65]   Involvement of proteasome in the dynamic assembly of the androgen receptor transcription complex [J].
Kang, ZG ;
Pirskanen, A ;
Jänne, OA ;
Palvimo, JJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (50) :48366-48371
[66]   XPD mutations prevent TFIIH-dependent transactivation by nuclear receptors and phosphorylation of RARα [J].
Keriel, A ;
Stary, A ;
Sarasin, A ;
Rochette-Egly, C ;
Egly, JM .
CELL, 2002, 109 (01) :125-135
[67]   PHOSPHORYLATION OF THE ADENOVIRUS E1A-ASSOCIATED 300 KDA PROTEIN IN RESPONSE TO RETINOIC ACID AND E1A DURING THE DIFFERENTIATION OF F9 CELLS [J].
KITABAYASHI, I ;
ECKNER, R ;
ARANY, Z ;
CHIU, R ;
GACHELIN, G ;
LIVINGSTON, DM ;
YOKOYAMA, KK .
EMBO JOURNAL, 1995, 14 (14) :3496-3509
[68]   Estrogen response element-dependent regulation of transcriptional activation of estrogen receptors α and β by coactivators and corepressors [J].
Klinge, CM ;
Jernigan, C ;
Mattingly, KA ;
Risinger, KE ;
Zhang, J .
JOURNAL OF MOLECULAR ENDOCRINOLOGY, 2004, 33 (02) :387-410
[69]   Synergistic enhancement of nuclear receptor function by p160 coactivators and two coactivators with protein methyltransferase activities [J].
Koh, SS ;
Chen, DG ;
Lee, YH ;
Stallcup, MR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (02) :1089-1098
[70]   Dimerization with retinoid x receptors and phosphorylation modulate the retinoic acid-induced degradation of retinoic acid receptors α and γ through the ubiquitin-proteasome pathway [J].
Kopf, E ;
Plassat, JL ;
Vivat, V ;
de Thé, H ;
Chambon, P ;
Rochette-Egly, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (43) :33280-33288