Cloning, characterization and expression of a functional mouse ACTH receptor

Biochem Biophys Res Commun. 1995 Jul 26;212(3):912-8. doi: 10.1006/bbrc.1995.2056.

Abstract

A polymerase chain reaction-generated mouse ACTH-R probe was used to screen a mouse genomic library, and a clone of 13kb containing the entire coding sequence was isolated. The coding sequence shows 84% homology with the human gene at the DNA level and encodes a peptide with 89% homology to the human ACTH-R. This gene is expressed as a major transcript of 1.8kb in the mouse adrenal gland. The gene was expressed in HeLa cells and cAMP production in response to either ACTH or alpha-MSH was measured. cAMP increased in an ACTH dose dependent manner suggesting an EC50 of 7 x 10(-10)M ACTH. alpha-MSH was without effect on this receptor. In conclusion we have cloned a mouse ACTH receptor gene and demonstrated for the first time its expression and functional effect in HeLa cells.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Cattle
  • Cloning, Molecular
  • Cyclic AMP / biosynthesis
  • DNA / genetics
  • Gene Expression
  • Genomic Library
  • HeLa Cells
  • Humans
  • Mice
  • Molecular Sequence Data
  • Polymerase Chain Reaction
  • Receptors, Corticotropin / genetics*
  • Receptors, Corticotropin / metabolism
  • Sequence Homology, Amino Acid
  • Species Specificity
  • Transfection

Substances

  • Receptors, Corticotropin
  • DNA
  • Cyclic AMP

Associated data

  • GENBANK/S78985