TY - JOUR
T1 - Hormone selectivity in thyroid hormone receptors
AU - Wagner, Richard L.
AU - Huber, B. Russell
AU - Shiau, Andrew K.
AU - Kelly, Alex
AU - Cunha Lima, Suzana T.
AU - Scanlan, Thomas S.
AU - Apriletti, James W.
AU - Baxter, John D.
AU - West, Brian L.
AU - Fletterick, Robert J.
PY - 2001
Y1 - 2001
N2 - Separate genes encode thyroid hormone receptor subtypes TRα (NR1A1) and TRβ (NR1A2). Products from each of these contribute to hormone action, but the subtypes differ in tissue distribution and physiological response. Compounds that discriminate between these subtypes in vivo may be useful in treating important medical problems such as obesity and hypercholesterolemia. We previously determined the crystal structure of the rat (r) TRα ligand-binding domain (LBD). In the present study, we determined the crystal structure of the rTRα LBD in a complex with an additional ligand, Triac (3,5, 3′-triiodothyroacetic acid), and two crystal structures of the human (h) TRβ receptor LBD in a complex with either Triac or a TRβ-selective compound, GC-1 [3,5-dimethyl-4-(4′-hydroy-3′-isopropylbenzyl)-phenoxy acetic acid]. The rTRα and hTRβ LBDs show close structural similarity. However, the hTRβ structures extend into the DNA-binding domain and allow definition of a structural "hinge" region of only three amino acids. The two TR subtypes differ in the loop between helices 1 and 3, which could affect both ligand recognition and the effects of ligand in binding coactivators and corepressors. The two subtypes also differ in a single amino acid residue in the hormone-binding pocket, Asn (TRβ) for Ser (TRα). Studies here with TRs in which the subtype-specific residue is exchanged suggest that most of the selectivity in binding derives from this amino acid difference. The flexibility of the polar region in the TRβ receptor, combined with differential recognition of the chemical group at the 1-carbon position, seems to stabilize the complex with GC-1 and contribute to itsβ-selectivity. These results suggest a strategy for development of subtype-specific compounds involving modifications of the ligand at the 1-position.
AB - Separate genes encode thyroid hormone receptor subtypes TRα (NR1A1) and TRβ (NR1A2). Products from each of these contribute to hormone action, but the subtypes differ in tissue distribution and physiological response. Compounds that discriminate between these subtypes in vivo may be useful in treating important medical problems such as obesity and hypercholesterolemia. We previously determined the crystal structure of the rat (r) TRα ligand-binding domain (LBD). In the present study, we determined the crystal structure of the rTRα LBD in a complex with an additional ligand, Triac (3,5, 3′-triiodothyroacetic acid), and two crystal structures of the human (h) TRβ receptor LBD in a complex with either Triac or a TRβ-selective compound, GC-1 [3,5-dimethyl-4-(4′-hydroy-3′-isopropylbenzyl)-phenoxy acetic acid]. The rTRα and hTRβ LBDs show close structural similarity. However, the hTRβ structures extend into the DNA-binding domain and allow definition of a structural "hinge" region of only three amino acids. The two TR subtypes differ in the loop between helices 1 and 3, which could affect both ligand recognition and the effects of ligand in binding coactivators and corepressors. The two subtypes also differ in a single amino acid residue in the hormone-binding pocket, Asn (TRβ) for Ser (TRα). Studies here with TRs in which the subtype-specific residue is exchanged suggest that most of the selectivity in binding derives from this amino acid difference. The flexibility of the polar region in the TRβ receptor, combined with differential recognition of the chemical group at the 1-carbon position, seems to stabilize the complex with GC-1 and contribute to itsβ-selectivity. These results suggest a strategy for development of subtype-specific compounds involving modifications of the ligand at the 1-position.
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U2 - 10.1210/mend.15.3.0608
DO - 10.1210/mend.15.3.0608
M3 - Article
C2 - 11222741
AN - SCOPUS:17744379363
SN - 0888-8809
VL - 15
SP - 398
EP - 410
JO - Molecular Endocrinology
JF - Molecular Endocrinology
IS - 3
ER -