Molecular cloning and functional analysis of the rat mu opioid receptor gene promoter

Biochem Biophys Res Commun. 1995 Oct 13;215(2):591-7. doi: 10.1006/bbrc.1995.2505.

Abstract

The rat mu opioid receptor gene promoter was cloned and characterized. It has a few features in common with the mouse gene, e.g. the lack of a classical TATA box and the fact that several transcriptional start sites are used. The overall homology between the two species is greater than 85%. Functional analysis of the promoter was performed using transient expression of rat mu opioid receptor-reporter gene constructs in the mu opioid receptor expressing cell line SH SY5Y and in non mu opioid receptor expressing cell lines. A promoter region was defined which confers both high basal and TPA and forskolin stimulated reporter gene expression in SH SY5Y cells.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Base Sequence
  • Brain / metabolism*
  • Cell Line
  • Chloramphenicol O-Acetyltransferase / biosynthesis
  • Cloning, Molecular
  • Genomic Library
  • Mice
  • Molecular Sequence Data
  • Plasmids
  • Promoter Regions, Genetic*
  • Rats
  • Receptors, Opioid, mu / biosynthesis*
  • Receptors, Opioid, mu / genetics*
  • Recombinant Proteins / biosynthesis
  • Restriction Mapping
  • Sequence Homology, Nucleic Acid
  • TATA Box
  • Transcription, Genetic
  • Transfection

Substances

  • Receptors, Opioid, mu
  • Recombinant Proteins
  • Chloramphenicol O-Acetyltransferase

Associated data

  • GENBANK/S79903