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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
Transcriptional Activation of Cytochrome P450 CYP2C45 by Drugs Is
Mediated by the Chicken Xenobiotic Receptor (CXR) Interacting with a
Phenobarbital Response Enhancer Unit*
Manuel
Baader ,
Carmela
Gnerre ,
John J.
Stegeman§, and
Urs A.
Meyer ¶
From the 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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Copyright © 2002 by the American Society for Biochemistry and Molecular Biology.
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