Opposite clinical phenotypes of glucokinase disease: Description of a novel activating mutation and contiguous inactivating mutations in human glucokinase (GCK) gene

Fabrizio Barbetti, Nadia Cobo-Vuilleumier, Carlo Dionisi-Vici, Sonia Toni, Paolo Ciampalini, Ornella Massa, Pablo Rodriguez-Bada, Carlo Colombo, Lorenzo Lenzi, María A. Garcia-Gimeno, Francisco J. Bermudez-Silva, Fernando Rodriguez De Fonseca, Patrizia Banin, Juan C. Aledo, Elena Baixeras, Pascual Sanz, Antonio L. Cuesta-Muñoz

Research output: Contribution to journalArticle

Abstract

Glucokinase is essential for glucose-stimulated insulin release from the pancreatic β-cell, serving as glucose sensor in humans. Inactivating or activating mutations of glucokinase lead to different forms of glucokinase disease, i.e. GCK-monogenic diabetes of youth, permanent neonatal diabetes (inactivating mutations), and congenital hyperinsulinism, respectively. Here we present a novel glucokinase gene (GCK)-activating mutation (p.E442K) found in an infant with neonatal hypoglycemia (1.5 mmol/liter) and in two other family members suffering from recurrent hypoglycemic episodes in their childhood and adult life. In contrast to the severe clinical presentation in the index case, functional studies showed only a slight activation of the protein (relative activity index of 3.3).We also report on functional studies of two inactivating mutations of the GCK (p.E440G and p.S441W), contiguous to the activating one, that lead to monogenic diabetes of youth. Interestingly, adult family members carrying the GCK pE440G mutation show an unusually heterogeneous and progressive diabetic phenotype, a feature not typical of GCK-monogenic diabetes of youth. In summary, we identified a novel activating GCK mutation that although being associated with severe neonatal hypoglycemia is characterized by the mildest activation of the glucokinase enzyme of all previously reported.

Original languageEnglish
Pages (from-to)1983-1989
Number of pages7
JournalMolecular Endocrinology
Volume23
Issue number12
DOIs
Publication statusPublished - Dec 2009

ASJC Scopus subject areas

  • Molecular Biology
  • Endocrinology

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    Barbetti, F., Cobo-Vuilleumier, N., Dionisi-Vici, C., Toni, S., Ciampalini, P., Massa, O., Rodriguez-Bada, P., Colombo, C., Lenzi, L., Garcia-Gimeno, M. A., Bermudez-Silva, F. J., De Fonseca, F. R., Banin, P., Aledo, J. C., Baixeras, E., Sanz, P., & Cuesta-Muñoz, A. L. (2009). Opposite clinical phenotypes of glucokinase disease: Description of a novel activating mutation and contiguous inactivating mutations in human glucokinase (GCK) gene. Molecular Endocrinology, 23(12), 1983-1989. https://doi.org/10.1210/me.2009-0094