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Mol Cell Biol ; 42(2): e0036321, 2022 02 17.
Artículo en Inglés | MEDLINE | ID: mdl-34871063

RESUMEN

Mutations in thyroid hormone receptor α (TRα), a ligand-inducible transcription factor, cause resistance to thyroid hormone α (RTHα). This disorder is characterized by tissue-specific hormone refractoriness and hypothyroidism due to the inhibition of target gene expression by mutant TRα-corepressor complexes. Using biophysical approaches, we show that RTHα-associated TRα mutants devoid of ligand-dependent transcription activation function unexpectedly retain the ability to bind thyroid hormone. Visualization of the ligand T3 within the crystal structure of a prototypic TRα mutant validates this notion. This finding prompted the synthesis of different thyroid hormone analogues, identifying a lead compound, ES08, which dissociates corepressor from mutant human TRα more efficaciously than T3. ES08 rescues developmental anomalies in a zebrafish model of RTHα and induces target gene expression in TRα mutation-containing cells from an RTHα patient more effectively than T3. Our observations provide proof of principle for developing synthetic ligands that can relieve transcriptional repression by the mutant TRα-corepressor complex for treatment of RTHα.


Asunto(s)
Proteínas Co-Represoras/genética , Expresión Génica/fisiología , Predisposición Genética a la Enfermedad/genética , Hormonas Tiroideas/metabolismo , Animales , Humanos , Mutación/genética , Fenotipo , Receptores de Hormona Tiroidea/genética , Receptores alfa de Hormona Tiroidea/metabolismo , Triyodotironina/genética
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