A shift in the ligand responsiveness of thyroid hormone receptor α induced by heterodimerization with retinoid X receptor α

FX Claret, T Antakly, M Karin… - Molecular and cellular …, 1996 - Am Soc Microbiol
Molecular and cellular biology, 1996Am Soc Microbiol
Abstract Thyroid hormone (T3) receptors (T3Rs) are ligand-modulated transcription factors
that bind to thyroid hormone response elements (T3REs) and mediate either positive or
negative transcriptional regulation of target genes. In addition, in response to ligand binding,
T3Rs can interfere with AP-1 activity and thereby inhibit transcription of AP-1-responsive
genes. T3Rs were recently shown to form heterodimers with retinoid X receptors (RXRs),
leading to increased binding to T3REs in vitro and potentiation of transcriptional responses …
Abstract
Thyroid hormone (T3) receptors (T3Rs) are ligand-modulated transcription factors that bind to thyroid hormone response elements (T3REs) and mediate either positive or negative transcriptional regulation of target genes. In addition, in response to ligand binding, T3Rs can interfere with AP-1 activity and thereby inhibit transcription of AP-1-responsive genes. T3Rs were recently shown to form heterodimers with retinoid X receptors (RXRs), leading to increased binding to T3REs in vitro and potentiation of transcriptional responses in vivo. Here we demonstrate that T3Rα forms stable heterodimers with RXRα in living cells. Most important, we describe a new role for RXRα in modulating ligand-dependent T3Rα activity: heterodimerization with RXRα greatly increases transcriptional interference with AP-1 activity, augments T3-dependent transcriptional activation, and potentiates the reversal of ligand-independent activation by T3Rα. In all three cases, the responses occur at substantially lower T3 concentrations when elicited by T3Rα plus RXRα than by T3Rα alone. In vitro, the binding of T3 decreases the DNA-binding activity of T3Rα homodimers but does not affect DNA binding by T3Rα: RXRα heterodimers. We provide evidence that increased activities of T3Rα at lower T3 concentrations are not due to changes in its T3 binding properties. Instead, the altered response could be mediated by either RXRα-induced conformational changes, increased stability of heterodimers over homodimers, especially following T3 binding, or both.
American Society for Microbiology