Apolipoprotein B amino acid 3611 substitution from arginine to glutamine creates the Ag (h/i) epitope: the polymorphism is not associated with differences in serum cholesterol and apolipoprotein B levels

Hum Genet. 1989 Jul;82(4):322-6. doi: 10.1007/BF00273990.

Abstract

A G- to A-DNA sequence change in exon 26 of the human apolipoprotein B (apo B) gene leads to a glutamine substitution for arginine at codon 3611 of the mature apolipo-protein B100 and causes a loss of an MspI site. In 106 Finnish individuals, a complete correspondence exists between this MspI polymorphic site and the Ag (h/i) immunochemical polymorphism. Linkage disequilibrium was found between this MspI polymorphic site and the apo B XbaI and EcoRI variable sites and the Ag (al/d) and (c/g) epitope pairs; there is apparent linkage equilibrium with the apo B PvuII variable site. Based on three population studies (samples from London. Finland and Italy), no significant association was found between this RFLP and serum cholesterol and apo B levels. These data suggest that the arginine 3611----glutamine 3611 substitution has no significant effect on apo B function.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Apolipoproteins B / blood
  • Apolipoproteins B / genetics*
  • Arginine / genetics
  • Blotting, Southern
  • Child
  • Cholesterol / blood*
  • Deoxyribonuclease HpaII
  • Deoxyribonucleases, Type II Site-Specific
  • Epitopes / genetics
  • Exons
  • Female
  • Glutamine / genetics
  • Humans
  • Male
  • Middle Aged
  • Mutation*
  • Polymorphism, Genetic*
  • Polymorphism, Restriction Fragment Length*

Substances

  • Apolipoproteins B
  • Epitopes
  • Glutamine
  • Arginine
  • Cholesterol
  • Deoxyribonuclease HpaII
  • Deoxyribonucleases, Type II Site-Specific