Dopaminergic and ligand-independent activation of steroid hormone receptors

Science. 1991 Dec 13;254(5038):1636-9. doi: 10.1126/science.1749936.

Abstract

The current view of how steroid hormone receptors affect gene transcription is that these receptors, on binding ligand, change to a state in which they can interact with chromatin and regulate transcription of target genes. Receptor activation is believed to be dependent only on this ligand-binding event. Selected steroid hormone receptors can be activated in a ligand-independent manner by a membrane receptor agonist, the neurotransmitter dopamine. In vitro, dopamine faithfully mimicked the effect of progesterone by causing a translocation of chicken progesterone receptor (cPR) from cytoplasm to nucleus. Dual activation by progesterone and dopamine was dissociable, and a serine residue in the cPR was identified that is not necessary for progesterone-dependent activation of cPR, but is essential for dopamine activation of this receptor.

MeSH terms

  • 2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine / pharmacology
  • Adenylyl Cyclases / physiology
  • Animals
  • Cell Line
  • Chlorocebus aethiops
  • Dopamine / pharmacology*
  • Epinephrine / pharmacology
  • Ergolines / pharmacology
  • Ethers, Cyclic / pharmacology
  • Gene Expression Regulation / drug effects
  • In Vitro Techniques
  • Isoproterenol / pharmacology
  • Ligands
  • Norepinephrine / pharmacology
  • Okadaic Acid
  • Promoter Regions, Genetic
  • Quinpirole
  • Receptors, Dopamine / physiology*
  • Receptors, Steroid / physiology*
  • Regulatory Sequences, Nucleic Acid
  • Signal Transduction
  • Transcription Factors / physiology
  • Transcription, Genetic / drug effects

Substances

  • Ergolines
  • Ethers, Cyclic
  • Ligands
  • Receptors, Dopamine
  • Receptors, Steroid
  • Transcription Factors
  • Okadaic Acid
  • Quinpirole
  • 2,3,4,5-Tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine
  • Adenylyl Cyclases
  • Isoproterenol
  • Dopamine
  • Norepinephrine
  • Epinephrine