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Molecular and Cellular Biology, October 1998, p. 5652-5658, Vol. 18, No. 10
Pharmacogenetics Section, Laboratory of
Reproductive and Developmental Toxicology, National Institute of
Environmental Health Sciences, National Institutes of Health, Research
Triangle Park, North Carolina 27709
Received 17 March 1998/Returned for modification 21 April
1998/Accepted 7 July 1998
PBREM, the phenobarbital-responsive enhancer module of the
cytochrome P-450 Cyp2b10 gene, contains two potential
nuclear receptor binding sites, NR1 and NR2. Consistent with the
finding that anti-retinoid X receptor (RXR) could supershift the
NR1-nuclear protein complex, DNA affinity chromatography with NR1
oligonucleotides enriched the nuclear orphan receptor RXR from the
hepatic nuclear extracts of phenobarbital-treated mice. In addition to
RXR, the nuclear orphan receptor CAR was present in the same enriched
fraction. In the phenobarbital-treated mice, the binding of both CAR
and RXR was rapidly increased before the induction of CYP2B10 mRNA. In
vitro-translated CAR bound to NR1, but only in the presence of
similarly prepared RXR. PBREM was synergistically activated by
transfection of CAR and RXR in HepG2 and HEK293 cells when the NR1 site
was functional. A CAR-RXR heterodimer has thus been characterized as a
trans-acting factor for the phenobarbital-inducible Cyp2b10 gene.
0270-7306/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
The Nuclear Orphan Receptor CAR-Retinoid X Receptor
Heterodimer Activates the Phenobarbital-Responsive Enhancer Module
of the CYP2B Gene

*
Corresponding author. Mailing address: Pharmacogenetics
Section, Laboratory of Reproductive and Developmental Toxicology, National Institute of Environmental Health Sciences, National Institutes of Health, Research Triangle Park, NC 27709. Phone: (919)
541-2404. Fax: (919) 541-0696. E-mail:
negishi{at}niehs.nih.gov.
Present address: Department of Pharmaceutics, University of Kuopio,
FIN-70211 Kuopio, Finland.
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