The stimulatory G protein α-subunit Gsα is imprinted in human thyroid glands: Implications for thyroid function in pseudohypoparathyroidism types 1A and 1B

Abstract

The stimulatory G protein α-subunit Gsα couples receptors to adenylyl cyclase and is required for hormone-stimulated cAMP generation. In Albright hereditary osteodystrophy, heterozygous G sα null mutations only lead to PTH, TSH, and gonadotropin resistance when inherited maternally [pseudohypoparathyroidism type 1A; (PHP1A)]. Maternal-specific expression of Gsα in specific hormone targets could explain this observation. Using hot-stop PCR analysis on total RNA from six normal human thyroid specimens, we showed that the majority of the Gsα mRNA (72 ± 3%) was derived from the maternal allele. This is consistent with the presence of TSH resistance in patients with maternal Gsα null mutations (PHP1A) and the absence of TSH resistance in patients with paternal Gsα mutations (pseudopseudohypoparathyroidism). Patients with PTH resistance in the absence of Albright hereditary osteodystrophy (PHPIB) have an imprinting defect of the Gsα gene resulting in both alleles having a paternal epigenotype, which would lead to a more moderate level of thyroid-specific Gsα deficiency. We found evidence of borderline TSH resistance in 10 of 22 PHPIB patients. This study provides further evidence for tissue-specific imprinting of Gsα in humans and provides a potential mechanism for mild to moderate TSH resistance in PHPIA and borderline resistance in some patients with PHPIB.