AHR1B, a new functional aryl hydrocarbon receptor in zebrafish:: tandem arrangement of ahr1b and ahr2 genes

被引:111
作者
Karchner, SI [1 ]
Franks, DG [1 ]
Hahn, ME [1 ]
机构
[1] Woods Hole Oceanog Inst, Dept Biol, Woods Hole, MA 02543 USA
关键词
aryl hydrocarbon receptor (AHR); dioxin; gene duplication; pufferfish; toxicology; zebrafish;
D O I
10.1042/BJ20050713
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 aryl hydrocarbon receptor (AHR) is a ligand-activated transcription factor that regulates gene expression following activation by TCDD (2,3,7,8-tetrachlorodibenzo-p-dioxin) or a variety of other synthetic and natural compounds. Previous studies have identified two AHR genes, AHR1 and AHR2, in zebrafish (Danio rerio), a widely used model species for studying vertebrate development and an emerging model in developmental toxicology. Zebratish AHR2 binds TCDD with high affinity, is transcriptionally active and has a major role in mediating the developmental toxicity of TCDD. Zebrafish AHR1 lacks the ability to bind TCDD and activate transcription, and has no known function. In the present study, we report a new zebrafish AHR, designated AHR1B, which shares 34% amino acid sequence identity with AHR1 (AHMA). The ahr1b gene resides on chromosome 22, adjacent to ahr2, whereas the ahr1a gene is located on chromosome 16. AHR1B is expressed in embryos as early as 24 hours post-fertilization and increases through the next 2 days, but expression is not inducible by TCDD. In contrast with the previously identified AHR1A, in vitro-expressed AHR1B protein exhibits specific, high-affinity binding of [H-3]TCDD. Furthennore, AHR1B is able to activate the transcription of a reporter gene under the control of AHR response elements with an efficacy comparable with that of AHR2, but with a higher EC50. We speculate that AHR1B may have a physiological role, such as in embryonic development, whereas AHR2 mediates the response to xenobiotics.
引用
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页码:153 / 161
页数:9
相关论文
共 53 条
[31]  
Lynch M, 2000, GENETICS, V154, P459
[32]   The aryl hydrocarbon receptor displaces p300 from E2F-dependent promoters and represses S phase-specific gene expression [J].
Marlowe, JL ;
Knudsen, ES ;
Schwemberger, S ;
Puga, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (28) :29013-29022
[33]   Loss of teratogenic response to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) in mice lacking the Ah (dioxin) receptor [J].
Mimura, J ;
Yamashita, K ;
Nakamura, K ;
Morita, M ;
Takagi, TN ;
Nakao, K ;
Ema, M ;
Sogawa, K ;
Yasuda, M ;
Katsuki, M ;
FujiiKuriyama, Y .
GENES TO CELLS, 1997, 2 (10) :645-654
[34]   Role of aryl hydrocarbon receptor-mediated induction of the CYP1 enzymes in environmental toxicity and cancer [J].
Nebert, DW ;
Dalton, TP ;
Okey, AB ;
Gonzalez, FJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (23) :23847-23850
[35]   Caenorhabditis elegans orthologs of the aryl hydrocarbon receptor and its heterodimerization partner the aryl hydrocarbon receptor nuclear translocator [J].
Powell-Coffman, JA ;
Bradfield, CA ;
Wood, WB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (06) :2844-2849
[36]   Aryl hydrocarbon receptor 2 mediates 2,3,7,8-tetrachlorodibenzo-p-dioxin developmental toxicity in zebrafish [J].
Prasch, AL ;
Teraoka, H ;
Carney, SA ;
Dong, W ;
Hiraga, T ;
Stegeman, JJ ;
Heideman, W ;
Peterson, RE .
TOXICOLOGICAL SCIENCES, 2003, 76 (01) :138-150
[37]  
PRASCH AL, 2005, TOXICOL SCI S1, V84, P18
[38]   Characterization of the aromatic hydrocarbon receptor gene and its expression in Atlantic tomcod [J].
Roy, NK ;
Wirgin, I .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1997, 344 (02) :373-386
[39]   Ah receptor signaling pathways [J].
Schmidt, JV ;
Bradfield, CA .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 1996, 12 :55-89
[40]   Aryl hydrocarbon receptor-dependent induction of Cyp1a1 by bilirubin in mouse hepatoma hepa 1c1c7 cells [J].
Sinal, CJ ;
Bend, JR .
MOLECULAR PHARMACOLOGY, 1997, 52 (04) :590-599