Characterization of the promoter region of the human melanocortin-1 receptor (MC1R) gene

Biochem Biophys Res Commun. 1999 Aug 27;262(2):452-60. doi: 10.1006/bbrc.1999.1228.

Abstract

We sequenced 3201 bp upstream from the ATG translation start codon of the human melanocortin-1 receptor (MC1R). A number of transcriptional initiation sites were detected over a region of approximately 600 base pairs upstream of the receptor coding region. These consist of GC-rich regions, each including SP-1 consensus binding motifs. Neither a TATA nor a CAAT box was found in this region. The 5'-flanking region also contains the consensus regulatory elements for AP-1, AP-2, and several E-boxes. Gel shift assays targeting the three GC boxes confirmed binding of SP-1. A promoter assay revealed that the minimal region exhibiting promoter activity was located between nucleotides -517 and -282 in human melanoma SK-Mel-2 cells. Further deletion from -517 to -447, which removed an SP-1 site, completely abolished luciferase activity. In conclusion, the MC1R promoter shares the characteristics of many other GPCR promoters. These characteristics include GC-rich sequence, lack of a TATA box, and binding of SP-1.

MeSH terms

  • Base Sequence
  • Cloning, Molecular
  • DNA Mutational Analysis
  • DNA-Binding Proteins / metabolism
  • Gene Expression Regulation
  • Genes, Reporter
  • Humans
  • Molecular Sequence Data
  • Promoter Regions, Genetic*
  • Protein Binding
  • Receptors, Corticotropin / genetics*
  • Receptors, Melanocortin
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sequence Deletion
  • Transcription, Genetic
  • Tumor Cells, Cultured

Substances

  • DNA-Binding Proteins
  • Receptors, Corticotropin
  • Receptors, Melanocortin

Associated data

  • GENBANK/AB026663