Retinoic acid signaling in mammalian eye development

被引:152
作者
Cvekl, Ales [1 ,2 ]
Wang, Wei-Lin [1 ]
机构
[1] Albert Einstein Coll Med, Dept Genet, Bronx, NY 10461 USA
[2] Albert Einstein Coll Med, Dept Ophthalmol & Visual Sci, Bronx, NY 10461 USA
关键词
anterior segment; lens; nuclear receptors; periocular mesenchyme; optic cup; retina; retinoic acid; vitamin A; THYROID-HORMONE RECEPTOR; CRYSTALLIN GENE-EXPRESSION; CREB-BINDING PROTEIN/P300; DEVELOPING MOUSE RETINA; UNION-OF-PHARMACOLOGY; ALPHA-B-CRYSTALLIN; VITAMIN-A TOXICITY; NULL MUTANT MICE; NUCLEAR RECEPTOR; RESPONSE ELEMENT;
D O I
10.1016/j.exer.2009.04.012
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Retinoic acid (RA) is a biologically active metabolite of vitamin A (retinol) that serves as a signaling molecule during a number of developmental and physiological processes. RA signaling plays multiple roles during embryonic eye development RA signaling is initially required for reciprocal interactions between the optic vesicle and invaginating lens placode. RA signaling promotes normal development of the ventral retina and optic nerve through its activities in the neural crest cell-derived periocular mesenchyme. RA coordinates these processes by regulating biological activities of a family of non-steroid hormone receptors, RAR alpha/beta/gamma, and RXR alpha/beta/gamma. These DNA-binding transcription factors recognize DNA as RAR/RXR heterodimers and recruit multiprotein transcriptional co-repressor complexes. RA-binding to RAR receptors induces a conformational change in the receptor, followed by the replacement of co-repressor with co-activator complexes. Inactivation of RAR alpha/beta/gamma receptors in the periocular mesenchyme abrogates anterior eye segment formation. This review summarizes recent genetic studies of RA signaling and progress in understanding the molecular mechanism of transcriptional co-activators that function with RAR/RXR. (c) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:280 / 291
页数:12
相关论文
共 147 条
[1]  
Allis C.D., 2007, Epigenetics, P23
[2]   Structure, function and modulation of retinoic acid receptor beta, a tumor suppressor [J].
Alvarez, Susana ;
Germain, Pierre ;
Alvarez, Rosana ;
Rodriguez-Barrios, Fatima ;
Gronemeyer, Hinrich ;
de Lera, Angel R. .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2007, 39 (7-8) :1406-1415
[3]   Disruption of retinoid-related orphan receptor β changes circadian behavior, causes retinal degeneration and leads to vacillans phenotype in mice [J].
André, E ;
Conquet, F ;
Steinmayr, M ;
Stratton, SC ;
Porciatti, V ;
Becker-André, M .
EMBO JOURNAL, 1998, 17 (14) :3867-3877
[4]   Sensory organs: Making and breaking the pre-placodal region [J].
Bailey, AP ;
Streit, A .
CURRENT TOPICS IN DEVELOPMENTAL BIOLOGY, VOL 72, 2006, 72 :167-+
[5]   TRANSGENIC MICE EXPRESSING A CONSTITUTIVELY ACTIVE RETINOIC ACID RECEPTOR IN THE LENS EXHIBIT OCULAR DEFECTS [J].
BALKAN, W ;
KLINTWORTH, GK ;
BOCK, CB ;
LINNEY, E .
DEVELOPMENTAL BIOLOGY, 1992, 151 (02) :622-625
[6]   Gene expression regulation by retinoic acid [J].
Balmer, JE ;
Blomhoff, R .
JOURNAL OF LIPID RESEARCH, 2002, 43 (11) :1773-1808
[7]   Three habits of highly effective signaling pathways: principles of transcriptional control by developmental cell signaling [J].
Barolo, S ;
Posakony, JW .
GENES & DEVELOPMENT, 2002, 16 (10) :1167-1181
[8]   Nuclear retinoid receptors and the transcription of retinoid-target genes [J].
Bastien, J ;
Rochette-Egly, C .
GENE, 2004, 328 :1-16
[9]  
Bäumer N, 2002, DEVELOPMENT, V129, P4535
[10]   Developmental abnormalities in cultured mouse embryos deprived of retinoic acid by inhibition of yolk-sac retinol binding protein synthesis [J].
Bavik, C ;
Ward, SJ ;
Chambon, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (07) :3110-3114