Evidence of a founder effect for the RETGC1 (GUCY2D) 2943DelG mutation in Leber congenital amaurosis pedigrees of Finnish origin

Hum Mutat. 2002 Oct;20(4):322-3. doi: 10.1002/humu.9067.

Abstract

Leber congenital amaurosis (LCA) is the earliest and most severe form of all inherited retinal dystrophies. It is a genetically heterogeneous condition as six disease-causing genes have been hitherto identified. Among them, RETGC1 (GUCY2D), is more frequently implicated in our series of LCA patients. Interestingly, 70 % of the families with RETGC1 mutations are originating from Mediterranean countries, the remaining families (30%) being originating from various countries across the world. Here, we report, the identification of the same homozygous RETGC1 nonsense mutation in three unrelated and non-consanguineous LCA families of Finnish origin, suggesting a founder effect. Interestingly, no linkage desequilibrium was found using polymorphic markers flanking the RETGC1 gene, supporting the view that the mutation is very ancient. Haplotype studies and Bayesian calculation point the founder mutation to 150 generations (95% credible interval 80-240 generations), i.e., 3000 years ago.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blindness / congenital
  • Blindness / enzymology
  • Blindness / genetics*
  • Cyclic GMP / metabolism
  • Female
  • Finland
  • Founder Effect*
  • Guanine*
  • Guanylate Cyclase / genetics
  • Humans
  • Linkage Disequilibrium / genetics
  • Male
  • Mutation / genetics*
  • Nuclear Family
  • Optic Atrophies, Hereditary / enzymology
  • Optic Atrophies, Hereditary / genetics*
  • Pedigree*
  • Polymorphism, Single Nucleotide / genetics
  • Sequence Deletion / genetics*

Substances

  • Guanine
  • Guanylate Cyclase
  • Cyclic GMP