Structural elements of an orphan nuclear receptor-DNA complex

被引:127
作者
Zhao, Q
Khorasanizadeh, S
Miyoshi, Y
Lazar, MA
Rastinejad, F [1 ]
机构
[1] Univ Virginia, Sch Med, Dept Pharmacol, Xray Crystallog Lab, Charlottesville, VA 22908 USA
[2] Univ Penn, Med Ctr, Dept Med, Div Endocrinol Diabet & Metab, Philadelphia, PA 19104 USA
[3] Univ Penn, Med Ctr, Dept Genet, Philadelphia, PA 19104 USA
[4] Univ Penn, Med Ctr, Dept Pharmacol, Philadelphia, PA 19104 USA
关键词
D O I
10.1016/S1097-2765(00)80084-2
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
The nuclear hormone receptors form the largest known family of transcription factors. The current notion of receptor DNA discrimination, based solely on one major type of hexameric half-site and a highly conserved be-residue core DNA-binding domain (DBD), does not adequately describe how more than 150 nonsteroid receptors differentiate among response elements. Here, we describe the 2.3 Angstrom crystal structure of the DNA-binding region of the orphan receptor RevErb arranged as a tandem homodimer on its optimal response element. The structure reveals the presence of a second major protein-DNA interface adjacent to the classical one involving the half-sites. A sequence comparison of orphan receptors suggests that unique minor-groove interactions involving the receptor hinge regions impart the necessary DNA and dimerization specificity.
引用
收藏
页码:849 / 861
页数:13
相关论文
共 64 条
[1]   Cross-validated maximum likelihood enhances crystallographic simulated annealing refinement [J].
Adams, PD ;
Pannu, NS ;
Read, RJ ;
Brunger, AT .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (10) :5018-5023
[2]   A NEW ORPHAN MEMBER OF THE NUCLEAR HORMONE-RECEPTOR SUPERFAMILY THAT INTERACTS WITH A SUBSET OF RETINOIC ACID RESPONSE ELEMENTS [J].
BAES, M ;
GULICK, T ;
CHOI, HS ;
MARTINOLI, MG ;
SIMHA, D ;
MOORE, DD .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (03) :1544-1552
[3]  
BILDER DW, 1995, GENOMICS, V14, P1087
[4]  
Brunger A.T., 1992, X-Plor Manual Version 3.1
[5]   RZRS, A NEW FAMILY OF RETINOID-RELATED ORPHAN RECEPTORS THAT FUNCTION AS BOTH MONOMERS HOMODIMERS [J].
CARLBERG, C ;
VANHUIJSDUIJNEN, RH ;
STAPLE, JK ;
DELAMARTER, JF ;
BECKERANDRE, M .
MOLECULAR ENDOCRINOLOGY, 1994, 8 (06) :757-770
[6]  
CHAWLA A, 1993, J BIOL CHEM, V268, P16265
[7]   The PPAR alpha-leukotriene B-4 pathway to inflammation control [J].
Devchand, PR ;
Keller, H ;
Peters, JM ;
Vazquez, M ;
Gonzalez, FJ ;
Wahli, W .
NATURE, 1996, 384 (6604) :39-43
[8]   Peroxisome proliferator-activated receptors and retinoic acid receptors differentially control the interactions of retinoid X receptor heterodimers with ligands, coactivators, and corepressors [J].
DiRenzo, J ;
Soderstrom, M ;
Kurokawa, R ;
Ogliastro, MH ;
Ricote, M ;
Ingrey, S ;
Horlein, A ;
Rosenfeld, MG ;
Glass, CK .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (04) :2166-2176
[9]   CONSTITUTIVE EXPRESSION OF THE ORPHAN RECEPTOR, REV-ERBA-ALPHA, INHIBITS MUSCLE DIFFERENTIATION AND ABROGATES THE EXPRESSION OF THE MYOD GENE FAMILY [J].
DOWNES, M ;
CAROZZI, AJ ;
MUSCAT, GEO .
MOLECULAR ENDOCRINOLOGY, 1995, 9 (12) :1666-1678
[10]   A NEW ORPHAN MEMBER OF THE NUCLEAR HORMONE-RECEPTOR SUPERFAMILY CLOSELY-RELATED TO REV-ERB [J].
DUMAS, B ;
HARDING, HP ;
CHOI, HS ;
LEHMANN, KA ;
CHUNG, M ;
LAZAR, MA ;
MOORE, DD .
MOLECULAR ENDOCRINOLOGY, 1994, 8 (08) :996-1005