Type 1 (insulin-dependent) diabetes and a highly variable locus close to the insulin gene on chromosome 11

Diabetologia. 1985 Apr;28(4):218-22. doi: 10.1007/BF00282236.

Abstract

A polymorphic DNA sequence in the 5'-flanking region of the human insulin gene was studied in relation to Type 1 (insulin-dependent) diabetes. In 141 Caucasoid subjects analysed by Southern blot hybridisation techniques, two major DNA insertions were observed: a Class 1 allele or a Class 3 allele. The Class 2 allele was not observed in this group of subjects. Genotype frequencies in a control population (n = 88) were: homozygous 1/1, 42%; heterozygous 1/3, 50%; and homozygous 3/3, 8%. Corresponding genotype frequencies in 53 Type 1 diabetic patients were 79%, 21% and 0%, respectively (p less than 0.0005 from chi 2 test). This confirms prevalence data reported by Bell et al. [16]. There appeared to be no coinheritance with HLA-DR3/DR4 related antigens, nor with autoimmune features. Analysis of 17 Type 1 diabetic pedigrees including 34 diabetic and 69 non-diabetic subjects did not demonstrate genetic linkage of these DNA inserts with diabetes, using an autosomal recessive, single locus model of inheritance.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles*
  • Chromosomes, Human, 6-12 and X
  • DNA Transposable Elements*
  • Diabetes Mellitus, Type 1 / genetics*
  • Female
  • Genetic Linkage*
  • Genotype
  • HLA-DR Antigens
  • Histocompatibility Antigens Class II / genetics
  • Humans
  • Insulin / genetics*
  • Male
  • Pedigree

Substances

  • DNA Transposable Elements
  • HLA-DR Antigens
  • Histocompatibility Antigens Class II
  • Insulin