Thyroid Hormone Receptors (TRs) are a class of intracellular nuclear proteins that function as ligand-dependent transcription factors, binding to the active thyroid hormone, triiodothyronine (T3), to regulate the expression of a vast array of target genes. These receptors are the molecular mediators of nearly all actions of thyroid hormones, profoundly influencing metabolism, development, and cellular differentiation across all tissues.
Origin
These receptors were discovered as part of the broader study of steroid and thyroid hormone action, which established a mechanism by which lipophilic hormones directly penetrate the cell and influence gene expression. The receptors are structurally classified as members of the nuclear receptor superfamily, alongside receptors for steroids and vitamin D.
Mechanism
Upon binding to T3, the thyroid hormone receptor typically forms a heterodimer complex with the Retinoid X Receptor (RXR) and then translocates to specific DNA sequences known as Thyroid Response Elements (TREs) in the promoter regions of target genes. This complex then recruits coactivator or corepressor proteins to either activate or repress the transcription of genes, thereby precisely controlling the basal metabolic rate and functional output of the cell.
Lifestyle changes epigenetically reshape cellular hormone receptor sensitivity, recalibrating the body's intricate communication systems for enhanced vitality.
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