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Polymorphic Analysis of the Human MHC‐Linked Heat Shock Protein 70 (HSP70‐2) and HSP70‐Hom Genes in Insulin‐Dependent Diabetes Mellitus (IDDM)
Author(s) -
POCIOT F.,
RØNNINGEN K. S.,
NERUP J.
Publication year - 1993
Publication title -
scandinavian journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.934
H-Index - 88
eISSN - 1365-3083
pISSN - 0300-9475
DOI - 10.1111/j.1365-3083.1993.tb02593.x
Subject(s) - allele , biology , haplotype , linkage disequilibrium , major histocompatibility complex , genotype , genetics , human leukocyte antigen , hsp70 , heat shock protein , immunology , gene , antigen
In the present study we characterized the frequencies of two polymorphisms within the MHC‐linked heat shock protein (HSP) 70 genes in patients with insulin‐dependent diabetes mellitus (IDDM) ( n= 114) and healthy control individuals (n = 110). Significant differences in genotype and allelic frequencies were observed for both polymorphisms between randomly selected patients and controls. However, for the HSP70‐2 polymorphisms this was solely due to linkage disequilibrium with DR3. The rare HSP70‐Hom 2‐allele was significantly more frequent in controls than in patients. It showed strong association with certain tumour necrosis factor (TNF) (class III) and HLA‐B and ‐A (class I) alleles independent of HLA‐DQ and ‐DR alleles. By typing 257 individuals from 55 IDDM multiple‐case families two extended MHC‐haplotypes, including class II‐, TNF‐ and class I‐markers, carrying the rare HSP70‐Hom allele were defined. One was only transmitted to diabetic offspring, whereas the other was only transmitted to unaffected offspring. The functional implication of the polymorphism in the heat shock‐inducible HSP70‐2 gene was analysed by studying HSP70‐2 mRNA expression after heat shock in peripheral blood mononuclear cells from individuals with different HSP70‐2 genotypes. Preliminary data showed that individuals homozygous for the PstI 8.5‐kb allele consistently had slightly lower expression than heterozygous and 9·0‐kb homozygous individuals.