Phenobarbital responsiveness conferred by the 5'-flanking region of the rat CYP2B2 gene in transgenic mice

Richard Ramsden, Nancy B. Beck, Karen M. Sommer, Curtis J. Omiecinski

Research output: Contribution to journalArticlepeer-review

36 Scopus citations


Phenobarbital (PB) is a prototype for a class of agents that produce marked transcriptional activation of a number of genes, including certain cytochrome P-450s. We used transgenic mouse approaches and multiple gene reporters to assess the functional consequences of specific deletions and site-specific mutations within the 2.5 kb 5'-flanking region of the rat CYP2B2 gene. Protein-DNA interactions at the PBRU domain also were characterized. Using the transgenic models, we demonstrate that sequences between -2500 and -1700 bp of the CYP2B2 gene are critical for PB induction; mice with 1700 or 800 bp of 5'-flanking CYP2B2 sequence are not PB responsive. DNA affinity enrichment techniques and immunoblotting and electromobility shift assays were used to determine that nuclear factor 1 (NF-1) interacts strongly with a site centered at -2200 bp in the PB responsive unit (PBRU) of CYP2B2. To test the functional contribution of NF- 1 in PB activation, we introduced specific mutations within the PBRU NF-1 element and demonstrated that these mutations completely ablate the binding interaction. However, transgenic mice incorporating the mutant NF-1 sequence within an otherwise wild-type -2500/CYP2B2 transgene maintained full PB responsiveness. These results indicate that, despite the avidity of the respective DNA-protein interaction within the PBRU in vitro, NF-1 interaction is not an essential factor directing PB transcriptional activation in vivo.

Original languageEnglish (US)
Pages (from-to)169-179
Number of pages11
Issue number1-2
StatePublished - Mar 4 1999

All Science Journal Classification (ASJC) codes

  • Genetics


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