Human Molecular Genetics, 2002, Vol. 11, No. 22 2741-2750
© 2002 Oxford University Press
Pseudohypoparathyroidism type Ib with disturbed imprinting in the GNAS1 cluster and Gs
deficiency in platelets
1Center for Molecular and Vascular Biology and 2Department of Pediatrics, University of Leuven, Belgium
Received June 13, 2002; Accepted August 8, 2002
Pseudohypoparathyroidism Ib (PHPIb), characterized by parathyroid hormone-resistant hypocalcemia and hyperphosphatemia, is caused by a deregulation in the imprinting status of the GNAS1 cluster, comprising exons XL, NESP55 and 1A and the coding exons of Gs
. Differences in methylation of exon 1A and sporadically also of exons XL and NESP55 were found and thought to result in long-range effects on Gs expression, limited to the proximal renal tubules. The exact imprinting defect is not precisely localized, and the expected differences in Gs protein level and function are mainly hypothetical. We describe a PHPIb patient with lack of methylation of the exon XL and 1A promoters, and biallelic methylation of the NESP55 promoter. Platelets of this patient show a functional Gs defect, decreased cAMP formation upon Gs-receptor stimulation, normal Gs sequence but reduced Gs protein levels. Transcriptional deregulation between the now biallelically active promoters of both exon 1A and exon 1 of Gs could explain the decreased Gs expression in platelets and presumably in the proximal renal tubules. We found decreased NESP55 and increased XLs protein levels in platelets, in agreement with the methylation status of their corresponding first exons. In a megakaryocytic cell line MEG-01, exon 1A is methylated on both alleles, in contrast to the normally maternally methylated exon 1A in leukocytes. Experimental demethylation of exon 1A in MEG-01 cells led to reduced Gs expression, in agreement with the observations in the patient. Platelet studies may therefore allow easy evaluation of disturbances of the GNAS1 cluster in PHPIb patients.
* To whom correspondence should be addressed at: Center for Molecular and Vascular Biology, UZ-Gasthuisberg, Herestraat 49, 3000 Leuven, Belgium. Tel: +32 16345775; Fax: +32 16345990; Email: christel.vangeet{at}uz.kuleuven.ac.be
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