Mechanism of the nuclear receptor molecular switch

被引:299
作者
Nagy, L
Schwabe, JWR
机构
[1] Univ Debrecen, Med & Hlth Sci Ctr, Res Ctr Mol Med, Dept Biochem & Mol Biol, H-4012 Debrecen, Hungary
[2] MRC, Mol Biol Lab, Cambridge CB2 2QH, England
基金
匈牙利科学研究基金会;
关键词
D O I
10.1016/j.tibs.2004.04.006
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
Nuclear receptors are central to the regulation of development, endocrine signalling and metabolism. The transcriptional activity of many receptors is controlled through the binding of small, fat-soluble molecules to the ligand-binding domain. In most cases, ligand binding turns the receptors into potent activators of transcription. This switch involves the exchange of co-regulator proteins that mediate transcriptional regulation. Structural and biochemical studies have together revealed the mechanism of action of this ligand-induced molecular switch, in which changes in the dynamic behaviour of the receptor play a key role. This remarkable dynamic mechanism has facilitated the evolution of a family of nuclear receptors with highly diverse ligand recognition and signalling properties.
引用
收藏
页码:317 / 324
页数:8
相关论文
共 70 条
[1]   The Drosophila orphan nuclear receptor DHR38 mediates an atypical ecdysteroid signaling pathway [J].
Baker, KD ;
Shewchuk, LM ;
Kozlova, T ;
Makishima, M ;
Hassell, A ;
Wisely, B ;
Caravella, JA ;
Lambert, MH ;
Reinking, JL ;
Krause, H ;
Thummel, CS ;
Willson, TM ;
Mangelsdorf, DJ .
CELL, 2003, 113 (06) :731-742
[2]   Molecular determinants of the balance between co-repressor and co-activator recruitment to the retinoic acid receptor [J].
Benko, S ;
Love, JD ;
Beládi, M ;
Schwabe, JWR ;
Nagy, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (44) :43797-43806
[3]   Crystal structure of the ligand-binding domain of the ultraspiracle protein USP, the ortholog of retinoid X receptors in insects [J].
Billas, IML ;
Moulinier, L ;
Rochel, N ;
Moras, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (10) :7465-7474
[4]   DNA binding domains in diverse nuclear receptors function as nuclear export signals [J].
Black, BE ;
Holaska, JM ;
Rastinejad, F ;
Paschal, BM .
CURRENT BIOLOGY, 2001, 11 (22) :1749-1758
[5]   CRYSTAL-STRUCTURE OF THE LIGAND-BINDING DOMAIN OF THE HUMAN NUCLEAR RECEPTOR RXR-ALPHA [J].
BOURGUET, W ;
RUFF, M ;
CHAMBON, P ;
GRONEMEYER, H ;
MORAS, D .
NATURE, 1995, 375 (6530) :377-382
[6]   Molecular basis of agonism and antagonism in the oestrogen receptor [J].
Brzozowski, AM ;
Pike, ACW ;
Dauter, Z ;
Hubbard, RE ;
Bonn, T ;
Engstrom, O ;
Ohman, L ;
Greene, GL ;
Gustafsson, JA ;
Carlquist, M .
NATURE, 1997, 389 (6652) :753-758
[7]   Role of CBP/P300 in nuclear receptor signalling [J].
Chakravarti, D ;
LaMorte, VJ ;
Nelson, MC ;
Nakajima, T ;
Schulman, IG ;
Juguilon, H ;
Montminy, M ;
Evans, RM .
NATURE, 1996, 383 (6595) :99-103
[8]   Nuclear receptors and lipid physiology: Opening the X-files [J].
Chawla, A ;
Repa, JJ ;
Evans, RM ;
Mangelsdorf, DJ .
SCIENCE, 2001, 294 (5548) :1866-1870
[9]   Nuclear receptor coactivator ACTR is a novel histone acetyltransferase and forms a multimeric activation complex with P/CAF and CBP/p300 [J].
Chen, HW ;
Lin, RJ ;
Schiltz, RL ;
Chakravarti, D ;
Nash, A ;
Nagy, L ;
Privalsky, ML ;
Nakatani, Y ;
Evans, RM .
CELL, 1997, 90 (03) :569-580
[10]   A TRANSCRIPTIONAL CO-REPRESSOR THAT INTERACTS WITH NUCLEAR HORMONE RECEPTORS [J].
CHEN, JD ;
EVANS, RM .
NATURE, 1995, 377 (6548) :454-457