A missense mutation in the glucagon receptor gene is associated with non-insulin-dependent diabetes mellitus

Nat Genet. 1995 Mar;9(3):299-304. doi: 10.1038/ng0395-299.

Abstract

Non-insulin-dependent diabetes mellitus (NIDDM) affects about 5% of the world population. The disease presents a polygenic mode of inheritance, but mechanisms and genes involved in late-onset NIDDM are largely unknown. We report the association of a single heterozygous Gly to Ser missense mutation in the glucagon receptor gene with late-onset NIDDM. This mutation was highly associated with NIDDM in a pooled set of French and Sardinian patients (chi 2 = 14.4, P = 0.0001) and showed some evidence for linkage to diabetes in 18 sibships from 9 French pedigrees (chi 2 = 6.63, P < 0.01). Receptor binding studies using cultured cells expressing the Gly40Ser mutation demonstrate that this mutation results in a receptor which binds glucagon with a three-fold lower affinity compared to the wild type receptor.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • DNA Primers / genetics
  • Diabetes Mellitus, Type 2 / genetics*
  • Diabetes Mellitus, Type 2 / metabolism
  • Female
  • Genetic Linkage
  • Glucagon / metabolism
  • Heterozygote
  • Humans
  • Male
  • Pedigree
  • Point Mutation*
  • Polymerase Chain Reaction
  • Polymorphism, Genetic
  • Polymorphism, Restriction Fragment Length
  • Receptors, Glucagon / genetics*
  • Receptors, Glucagon / metabolism

Substances

  • DNA Primers
  • Receptors, Glucagon
  • Glucagon