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