Regulatory interactions among three members of the vertebrate aryl hydrocarbon receptor family: AHR repressor, AHR1, and AHR2

被引:107
作者
Karchner, SI [1 ]
Franks, DG [1 ]
Powell, WH [1 ]
Hahn, ME [1 ]
机构
[1] Woods Hole Oceanog Inst, Dept Biol, Woods Hole, MA 02543 USA
关键词
D O I
10.1074/jbc.M110779200
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 effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) and related compounds occur via the aryl hydrocarbon receptor (AHR), a member of the basic helix-loop-helix-Per-ARNT-Sim homology (bHLH-PAS) protein superfamily. A single AHR gene has been identified in mammals, whereas many fish species, including the Atlantic killifish (Fundulus heteroclitus) possess two distinct AHR genes (AHR1 and a novel form, AHR2). A mouse bHLH-PAS protein closely related to AHR and designated AHR repressor (AHRR) is induced by 3-methylcholanthrene and represses the transcriptional activity of the AHR. To determine whether AHRR is the mammalian ortholog of fish AHR2 and to investigate the mechanisms by which AHRR regulates AHR function, we cloned an AHRR ortholog in F. heteroclitus with high sequence identity to the mouse and human AHRRs. Killifish AHRR encodes a 680-residue protein with a predicted molecular mass of 75.2 kDa. We show that in vitro expressed AHRR proteins from human, mouse, and killifish all fail to bind [H-3]TCDD or [H-3]beta-naphthoflavone. In transient transfection experiments using a luciferase reporter gene under control of AHR response elements, killifish AHRR inhibited the TCDD-dependent transactivation function of both AHR1 and AHR2. AHRR mRNA is widely expressed in killifish tissues and is inducible by TCDD or polychlorinated biphenyls, but its expression is not altered in a population of fish exhibiting genetic resistance to these compounds. The F. heteroclitus AHRR promoter contains three putative AHR response elements. Both AHR1 and AHR2 activated transcription of luciferase driven by the AHRR promoter, and AHRR could repress its own promoter. Thus, AHRR is an evolutionarily conserved, TCDD-inducible repressor of AHR1 and AHR2 function. Phylogenetic analysis shows that AHRR, AHR1, and AHR2 are distinct genes, members of an AHR gene family; these three vertebrate AHR-like genes descended from a single invertebrate AHR.
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页码:6949 / 6959
页数:11
相关论文
共 83 条
[1]   Two forms of aryl hydrocarbon receptor type 2 in rainbow trout (Oncorhynchus mykiss) -: Evidence for differential expression and enhancer specificity [J].
Abnet, CC ;
Tanguay, RL ;
Hahn, ME ;
Heideman, W ;
Peterson, RE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (21) :15159-15166
[2]   Structure and expression of the Ah receptor repressor gene [J].
Baba, T ;
Mimura, J ;
Gradin, K ;
Kuroiwa, A ;
Watanabe, T ;
Matsuda, Y ;
Inazawa, J ;
Sogawa, K ;
Fujii-Kuriyama, Y .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (35) :33101-33110
[3]   The syntenic relationship of the zebrafish and human genomes [J].
Barbazuk, WB ;
Korf, I ;
Kadavi, C ;
Heyen, J ;
Tate, S ;
Wun, E ;
Bedell, JA ;
McPherson, JD ;
Johnson, SL .
GENOME RESEARCH, 2000, 10 (09) :1351-1358
[4]   Acquired resistance to Ah receptor agonists in a population of Atlantic killifish (Fundulus heteroclitus) inhabiting a marine superfund site:: In vivo and in vitro studies on the inducibility of xenobiotic metabolizing enzymes [J].
Bello, SM ;
Franks, DG ;
Stegeman, JJ ;
Hahn, ME .
TOXICOLOGICAL SCIENCES, 2001, 60 (01) :77-91
[5]  
BOUCHER PD, 1995, MOL CELL BIOL, V15, P5144
[6]   CLONING OF THE AH-RECEPTOR CDNA REVEALS A DISTINCTIVE LIGAND-ACTIVATED TRANSCRIPTION FACTOR [J].
BURBACH, KM ;
POLAND, A ;
BRADFIELD, CA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (17) :8185-8189
[7]   An aryl hydrocarbon receptor (AHR) homologue from the soft-shell clam, Mya arenaria:: evidence that invertebrate AHR homologues lack 2,3,7,8-tetrachlorodibenzo-p-dioxin and β-naphthoflavone binding [J].
Butler, RA ;
Kelley, ML ;
Powell, WH ;
Hahn, ME ;
Van Beneden, RJ .
GENE, 2001, 278 (1-2) :223-234
[8]   DIOXIN-DEPENDENT ACTIVATION OF MURINE CYP1A-1 GENE-TRANSCRIPTION REQUIRES PROTEIN KINASE-C-DEPENDENT PHOSPHORYLATION [J].
CARRIER, F ;
OWENS, RA ;
NEBERT, DW ;
PUGA, A .
MOLECULAR AND CELLULAR BIOLOGY, 1992, 12 (04) :1856-1863
[9]  
CARVER LA, 1994, J BIOL CHEM, V269, P30109
[10]   Cross-talk between the aryl hydrocarbon receptor and hypoxia inducible factor signaling pathways - Demonstration of competition and compensation [J].
Chan, WK ;
Yao, G ;
Gu, YZ ;
Bradfield, CA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (17) :12115-12123