A base mutation of the C-erbAβ thyroid hormone receptor in a kindred with generalized thyroid hormone resistance. Molecular heterogeneity in two other kindreds

Generalized thyroid hormone resistance (GTHR) is a disorder of thyroid hormone action that we have previously shown to be tightly linked to one of the two thyroid hormone receptor genes, c-erbAβ, in a single kindred, A. We now show that in two other kindreds, B and D, with differing phenotypes, there is also linkage between c-erbAβ and GTHR. The combined maximum logarithm of the odds score for all three kindreds at a recombination fraction of 0 was 5.77. In vivo studies had shown a triiodothyronine (T₃)-binding affinity abnormality in nuclear receptors of kindred A, and we therefore investigated the defect in c-erbAβ in this kindred by sequencing a major portion of the T₃-binding domain in the 3'-region of fibroblast c-erbAβ cDNA and leukocyte c-erbAβ genomic DNA. A base substitution, cytosine to adenine, was found at cDNA position 1643 which altered the proline codon at position 448 to a histidine. By allelic-specific hybridization, this base substitution was found in only one allele of seven affected members, and not found in 10 unaffected members of kindred A, as expected for a dominant disease. Also, this altered base was not found in kindreds B or D, or in 92 random c-erbAβ alleles. These results and the fact that the mutation is predicted to alter the secondary structure of the crucial T₃-binding domain of the c-erbAβ receptor suggest this mutation is an excellent candidate for the genetic cause of GTHR in kindred A. Different mutations in the c-erbAβ gene are likely responsible for the variant phenotypes of thyroid hormone resistance in kindreds B and D.