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Originally published In Press as doi:10.1074/jbc.M109882200 on February 26, 2002

J. Biol. Chem., Vol. 277, Issue 18, 15647-15653, May 3, 2002
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Transcriptional Activation of Cytochrome P450 CYP2C45 by Drugs Is Mediated by the Chicken Xenobiotic Receptor (CXR) Interacting with a Phenobarbital Response Enhancer Unit*

Manuel BaaderDagger , Carmela GnerreDagger , John J. Stegeman§, and Urs A. MeyerDagger

From the Dagger  Department of Pharmacology/Neurobiology, Biozentrum of the University of Basel, Klingelbergstrasse 50/70, CH-4056 Basel, Switzerland and the § Department of Biology, Woods Hole Oceanographic Institution, Woods Hole, Massachusetts 02543

Cytochromes P450 (CYP)-2C enzymes fulfill an important role in xenobiotic metabolism and therefore have extensively been studied in rodents and humans. However, no CYP2C genes have been described in avian species to date. In this paper, we report the cloning, functional analysis, and regulation of chicken CYP2C45. The sequence shares up to 58% amino acid identity with CYP2Cs in other species. The overexpression of CYP2C45 in chicken hepatoma cells leghorn male hepatoma (LMH) led to increased scoparone metabolism. CYP2C45 regulation was studied in LMH cells at the mRNA level and in reporter gene assays using a construct containing 2.6 kb of its 5'-flanking region. Exposure of LMH cells to phenobarbital or metyrapone led to a 95- or 210-fold increase in CYP2C45 mRNA and a 140- or 290-fold increase in reporter gene expression, respectively. A phenobarbital response enhancer unit (PBRU) of 239 bp containing a DR-4 nuclear receptor binding site was identified within the 2.6-kb fragment. Site-specific mutation of the DR-4 revealed the requirement of this motif for CYP2C45 induction by drugs. The chicken xenobiotic receptor CXR interacted with the PBRU in electromobility shift and transactivation assays. Furthermore, the related nuclear receptors, mouse PXR and mouse CAR, transactivated this enhancer element, suggesting evolutionary conservation of nuclear receptor-DNA interactions in CYP2C induction.


* This work was supported by the Swiss National Science Foundation and by National Institutes of Health Grant P42 ES07381 (J. J. S.).The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

The nucleotide sequence(s) reported in this paper has been submitted to the GenBankTM/EBI Data Bank with accession number(s) .

To whom correspondence should be addressed. Tel.: 41-61-267-22-20; Fax: 41-61-267-22-08; E-mail: Urs-A.Meyer@unibas.ch.


Copyright © 2002 by The American Society for Biochemistry and Molecular Biology, Inc.
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