Crx, a novel Otx-like paired-homeodomain protein, binds to and transactivates photoreceptor cell-specific genes

被引:590
作者
Chen, SM
Wang, QL
Nie, ZQ
Sun, H
Lennon, G
Copeland, NG
Gilbert, DJ
Jenkins, NA
Zack, DJ
机构
[1] JOHNS HOPKINS UNIV,SCH MED,WILMER INST,BALTIMORE,MD 21287
[2] JOHNS HOPKINS UNIV,SCH MED,DEPT MOL BIOL & GENET,BALTIMORE,MD 21287
[3] JOHNS HOPKINS UNIV,SCH MED,DEPT NEUROSCI,BALTIMORE,MD 21287
[4] LAWRENCE LIVERMORE NATL LAB,CTR HUMAN GENOME,LIVERMORE,CA 94550
[5] NCI,FREDERICK CANC RES & DEV CTR,MAMMALIAN GENET LAB,ABL BASIC RES PROGRAM,FREDERICK,MD 21702
关键词
D O I
10.1016/S0896-6273(00)80394-3
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The otd/Otx gene family encodes paired-like homeodomain proteins that are involved in the regulation of anterior head structure and sensory organ development. Using the yeast one-hybrid screen with a bait containing the Ret 4 site from the bovine rhodopsin promoter, we have cloned a new member of the family, Crx (Cone rod homeobox). Crx encodes a 299 amino acid residue protein with a paired-like homeodomain near its N terminus. In the adult, it is expressed predominantly in photoreceptors and pinealocytes. In the developing mouse retina, it is expressed by embryonic day 12.5 (E12.5). Recombinant Crx binds in vitro not only to the Ret 4 site but also to the Ret 1 and BAT-1 sites. In transient transfection studies, Crx transactivates rhodopsin promoter-reporter constructs. Its activity is synergistic with that of Nr1. Crx also binds to and transactivates the genes for several other photoreceptor cell-specific proteins (interphotoreceptor retinoid-binding protein, beta-phosphodiesterase, and arrestin). Human Crx maps to chromosome 19q13.3, the site of a cone rod dystrophy (CORDII). These studies implicate Crx as a potentially important regulator of photoreceptor cell development and gene expression and also identify it as a candidate gene for CORDII and other retinal diseases.
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收藏
页码:1017 / 1030
页数:14
相关论文
共 78 条
[21]   MURINE AND BOVINE BLUE CONE PIGMENT GENES - CLONING AND CHARACTERIZATION OF 2 NEW MEMBERS OF THE S-FAMILY OF VISUAL PIGMENTS [J].
CHIU, MI ;
ZACK, DJ ;
WANG, YS ;
NATHANS, J .
GENOMICS, 1994, 21 (02) :440-443
[22]   DEVELOPMENT AND APPLICATIONS OF A MOLECULAR GENETIC-LINKAGE MAP OF THE MOUSE GENOME [J].
COPELAND, NG ;
JENKINS, NA .
TRENDS IN GENETICS, 1991, 7 (04) :113-118
[23]  
DesJardin LE, 1996, INVEST OPHTH VIS SCI, V37, P154
[24]  
DiPolo A, 1996, INVEST OPHTH VIS SCI, V37, P551
[25]   GENETIC-LINKAGE OF CONE-ROD RETINAL DYSTROPHY TO CHROMOSOME 19Q AND EVIDENCE FOR SEGREGATION DISTORTION [J].
EVANS, K ;
FRYER, A ;
INGLEHEARN, C ;
DUVALLYOUNG, J ;
WHITTAKER, JL ;
GREGORY, CY ;
BUTLER, R ;
EBENEZER, N ;
HUNT, DM ;
BHATTACHARYA, S .
NATURE GENETICS, 1994, 6 (02) :210-213
[26]   CHROMOSOME 19Q CONE-ROD RETINAL DYSTROPHY - OCULAR PHENOTYPE [J].
EVANS, K ;
DUVALLYOUNG, J ;
FITZKE, FW ;
ARDEN, GB ;
BHATTACHARYA, SS ;
BIRD, AC .
ARCHIVES OF OPHTHALMOLOGY, 1995, 113 (02) :195-201
[27]   THE ORTHODENTICLE GENE ENCODES A NOVEL HOMEO DOMAIN PROTEIN INVOLVED IN THE DEVELOPMENT OF THE DROSOPHILA NERVOUS-SYSTEM AND OCELLAR VISUAL STRUCTURES [J].
FINKELSTEIN, R ;
SMOUSE, D ;
CAPACI, TM ;
SPRADLING, AC ;
PERRIMON, N .
GENES & DEVELOPMENT, 1990, 4 (09) :1516-1527
[28]   FROM FLY HEAD TO MAMMALIAN FOREBRAIN - THE STORY OF OTD AND OTX [J].
FINKELSTEIN, R ;
BONCINELLI, E .
TRENDS IN GENETICS, 1994, 10 (09) :310-315
[29]   Transcription factor genes and the developing eye: A genetic perspective [J].
Freund, C ;
Horsford, DJ ;
McInnes, RR .
HUMAN MOLECULAR GENETICS, 1996, 5 :1471-1488
[30]   rax, a novel paired-type homeobox gene, shows expression in the anterior neural fold and developing retina [J].
Furukawa, T ;
Kozak, CA ;
Cepko, CL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (07) :3088-3093