Steroid receptor isoforms: exception or rule?

被引:39
作者
Keightley, MC [1 ]
机构
[1] Baylor Coll Med, Dept Cell Biol, Houston, TX 77030 USA
关键词
steroid receptors; progesterone receptor; isoforms;
D O I
10.1016/S0303-7207(97)00236-0
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Since the first steroid receptor was cloned, it was quickly identified as one of many such receptors constituting a gene superfamily which has grown to include not only steroid receptors but also receptors for thyroid hormone, retinoic acid, 1,25-dihydroxyvitamin D3 as well as a number of less traditional ligands, including farnesoids and fatty acids. Interestingly, these receptors are far outnumbered by the 'orphan' receptors for which ligands are still being sought. The orignal cloning of nuclear receptors, although sometimes identifying more than one receptor form, led to the general premise that each ligand has its cognate receptor through which signal is transduced to the transcriptional machinery. Regulation of this process was found to occur at the level of receptor expression, ligand availability, and more recently, through post-translational modifications of the receptor and interaction of a variety of coactivators/corepressors with the receptor protein. The continuing identification of more than a single form for many of the receptors directed the attention of a number of investigators toward defining possible roles for these 'extras'. This review examines the different forms of nuclear receptor gene family members and how they may provide an additional level of regulation. (C) 1998 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:1 / 5
页数:5
相关论文
共 51 条
[1]   CLONING OF HUMAN MINERALOCORTICOID RECEPTOR COMPLEMENTARY-DNA - STRUCTURAL AND FUNCTIONAL KINSHIP WITH THE GLUCOCORTICOID RECEPTOR [J].
ARRIZA, JL ;
WEINBERGER, C ;
CERELLI, G ;
GLASER, TM ;
HANDELIN, BL ;
HOUSMAN, DE ;
EVANS, RM .
SCIENCE, 1987, 237 (4812) :268-275
[2]   THE PROGESTERONE ANTAGONIST RU486 ACQUIRES AGONIST ACTIVITY UPON STIMULATION OF CAMP SIGNALING PATHWAYS [J].
BECK, CA ;
WEIGEL, NL ;
MOYER, ML ;
NORDEEN, SK ;
EDWARDS, DP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (10) :4441-4445
[3]   IDENTIFICATION OF A SPLICE VARIANT OF THE RAT AND HUMAN MINERALOCORTICOID RECEPTOR GENES [J].
BLOEM, LJ ;
GUO, CL ;
PRATT, JH .
JOURNAL OF STEROID BIOCHEMISTRY AND MOLECULAR BIOLOGY, 1995, 55 (02) :159-162
[4]   THE CONTRIBUTION OF THE N-TERMINAL AND C-TERMINAL REGIONS OF STEROID-RECEPTORS TO ACTIVATION OF TRANSCRIPTION IS BOTH RECEPTOR AND CELL-SPECIFIC [J].
BOCQUEL, MT ;
KUMAR, V ;
STRICKER, C ;
CHAMBON, P ;
GRONEMEYER, H .
NUCLEIC ACIDS RESEARCH, 1989, 17 (07) :2581-2595
[5]   A FUNCTIONAL PROMOTER DIRECTING EXPRESSION OF A NOVEL TYPE OF RAT MINERALOCORTICOID RECEPTOR MESSENGER-RNA IN BRAIN [J].
CASTREN, M ;
DAMM, K .
JOURNAL OF NEUROENDOCRINOLOGY, 1993, 5 (04) :461-466
[6]  
CONNEELY OM, 1989, J BIOL CHEM, V264, P14062
[7]   THE STEROID AND THYROID-HORMONE RECEPTOR SUPERFAMILY [J].
EVANS, RM .
SCIENCE, 1988, 240 (4854) :889-895
[8]   CHARACTERIZATION AND COLOCALIZATION OF STEROID BINDING AND DIMERIZATION ACTIVITIES IN THE MOUSE ESTROGEN-RECEPTOR [J].
FAWELL, SE ;
LEES, JA ;
WHITE, R ;
PARKER, MG .
CELL, 1990, 60 (06) :953-962
[9]   Recessive resistance to thyroid hormone in mice lacking thyroid hormone receptor beta: Evidence for tissue-specific modulation of receptor function [J].
Forrest, D ;
Hanebuth, E ;
Smeyne, RJ ;
Everds, N ;
Stewart, CL ;
Wehner, JM ;
Curran, T .
EMBO JOURNAL, 1996, 15 (12) :3006-3015
[10]  
FUQUA SAW, 1993, J CELL BIOCHEM, P194