The Nuclear Orphan Receptor CAR-Retinoid X Receptor Heterodimer Activates the Phenobarbital-Responsive Enhancer Module of the CYP2B Gene

Autor: Masahiko Negishi, Tatsuya Sueyoshi, Paavo Honkakoski, Igor Zelko
Rok vydání: 1998
Předmět:
Male
Time Factors
Receptors
Retinoic Acid

Molecular Sequence Data
Receptors
Cytoplasmic and Nuclear

Gene Expression
Biology
Retinoid X receptor
Mice
Cytochrome P-450 Enzyme System
Constitutive androstane receptor
Tumor Cells
Cultured

Animals
Humans
Amino Acid Sequence
Cytochrome P450 Family 2
Molecular Biology
Transcription factor
Cells
Cultured

Constitutive Androstane Receptor
Nuclear receptor co-repressor 1
Orphan receptor
Pregnane X receptor
Binding Sites
Cell Biology
Molecular biology
Neuron-derived orphan receptor 1
body regions
Mice
Inbred C57BL

Enhancer Elements
Genetic

Retinoid X Receptors
nervous system
Gene Expression Regulation
Nuclear receptor
Phenobarbital
Steroid Hydroxylases
embryonic structures
Trans-Activators
lipids (amino acids
peptides
and proteins)

Aryl Hydrocarbon Hydroxylases
Dimerization
hormones
hormone substitutes
and hormone antagonists

Transcription Factors
Zdroj: Molecular and Cellular Biology. 18:5652-5658
ISSN: 1098-5549
DOI: 10.1128/mcb.18.10.5652
Popis: 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.
Databáze: OpenAIRE