GNAS Defects Identified by Stimulatory G Protein α-Subunit Signalling Studies in Platelets

Abstract

Context: GNAS is an imprinted region that gives rise to several transcripts, antisense transcripts, and noncoding RNAs, including transcription of RNA encoding the α-subunit of the stimulatory G protein (Gsα). The complexity of the GNAS cluster results in ubiquitous genomic imprints, tissue-specific Gsα expression, and multiple genotype-phenotype relationships. Phenotypes resulting from genetic and epigenetic abnormalities of the GNAS region include Albright’s hereditary osteodystrophy, pseudohypoparathyroidism types Ia (PHPIa) and Ib (PHPIb), and pseudopseudohypoparathyroidism (PPHP).Objective: The aim was to study the complex GNAS pathology by a functional test as an alternative to the generally used but labor-intensive erythrocyte complementation assay.Design and Patients: We report the first platelet-based diagnostic test for Gsα hypofunction, supported by clinical, biochemical, and molecular data for six patients with PHPIa or PPHP and nine patients with PHPIb. The platelet test is based on the inhibition of platelet aggregation by cAMP, produced after Gsα stimulation.Results: Platelets are easily accessible, and platelet aggregation responses were found to reflect Gsα signaling defects in patients, in concordance with the patient’s phenotype and genotype. Gsα hypofunction in PHPIa and PPHP patients with GNAS mutations was clearly detected by this method. Mildly decreased or normal Gsα function was detected in patients with PHPIb with either an overall or exon 1A-only epigenetic defect, respectively. Platelet Gsα expression was reduced in both PHPIb patient groups, whereas XLαs was up-regulated only in PHPIb patients with the broad epigenetic defect.Conclusion: The platelet-based test is a novel tool for establishing the diagnosis of Gsα defects, which may otherwise be quite challenging.