Activation and repression by nuclear hormone receptors: hormone modulates an equilibrium between active and repressive states

Mol Cell Biol. 1996 Jul;16(7):3807-13. doi: 10.1128/MCB.16.7.3807.

Abstract

Transactivation-defective retinoid X and thyroid hormone receptors have been used to examine mechanisms of hormonal activation. Activation and repression of transcription by retinoid X and thyroid hormone receptors are shown to be mediated by physically distinct and functionally independent regions of the hormone binding domain. Nevertheless, the ability of receptors to respond to hormone requires communication between both functional domains. Deletion of the hormone-dependent transactivation function of the retinoid X receptor, the common subunit of heterodimeric nuclear receptors, significantly impairs hormone-dependent transcription by retinoic acid, thyroid hormone, and vitamin D receptors. The results indicate that receptors do not exist in static off and on conformations but that hormone alters an equilibrium between inactive and active states.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Cell Line
  • Chlorocebus aethiops
  • Cholecalciferol / pharmacology*
  • DNA-Binding Proteins / biosynthesis
  • DNA-Binding Proteins / drug effects
  • DNA-Binding Proteins / metabolism
  • Humans
  • Kinetics
  • Macromolecular Substances
  • Models, Structural
  • Polymerase Chain Reaction
  • Protein Conformation
  • Receptors, Retinoic Acid / biosynthesis
  • Receptors, Retinoic Acid / drug effects
  • Receptors, Retinoic Acid / metabolism*
  • Receptors, Thyroid Hormone / biosynthesis
  • Receptors, Thyroid Hormone / drug effects
  • Receptors, Thyroid Hormone / metabolism*
  • Recombinant Fusion Proteins / biosynthesis
  • Recombinant Fusion Proteins / drug effects
  • Recombinant Fusion Proteins / metabolism
  • Retinoid X Receptors
  • Transcription Factors / biosynthesis
  • Transcription Factors / drug effects
  • Transcription Factors / metabolism*
  • Transcriptional Activation* / drug effects
  • Transfection
  • Triiodothyronine / pharmacology*
  • beta-Galactosidase / biosynthesis

Substances

  • DNA-Binding Proteins
  • Macromolecular Substances
  • Receptors, Retinoic Acid
  • Receptors, Thyroid Hormone
  • Recombinant Fusion Proteins
  • Retinoid X Receptors
  • Transcription Factors
  • Triiodothyronine
  • Cholecalciferol
  • beta-Galactosidase