Tight linkage between myotonic dystrophy and apolipoprotein E genes revealed with allele-specific oligonucleotides

Hum Genet. 1988 Sep;80(1):49-52. doi: 10.1007/BF00451455.

Abstract

In 16 families with myotonic dystrophy (DM) a novel approach based on use of allele-specific oligonucleotides has been employed to study the linkage relationship between the apolipoprotein E (APOE) gene and DM. Synthetic oligonucleotides, designed to discriminate between APOE alleles epsilon 3 and epsilon 4, enabled us to distinguish heterozygous carriers in a hybridization assay. In a subset of families, the relevant segment of the APOE gene was enzymatically amplified to increase the sensitivity of the method. For DM and APOE, a maximum lod score (zmax of 7.47 was obtained at a recombination frequency (theta) of 0.047 (male theta = female theta). No recombination (maximum lod score of 5.61 at theta = 0.0) was found between APOE and the apolipoprotein CII (APOC2) gene. These results suggest that, in addition to APOC2, APOE is a useful marker for presymptomatic DM diagnosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles*
  • Amino Acid Sequence
  • Apolipoproteins E / genetics*
  • Base Sequence
  • DNA / blood
  • DNA / genetics
  • Gene Amplification
  • Genes*
  • Genetic Linkage*
  • Humans
  • Molecular Sequence Data
  • Myotonic Dystrophy / blood
  • Myotonic Dystrophy / genetics*
  • Nucleic Acid Hybridization
  • Oligodeoxyribonucleotides
  • Polymorphism, Genetic

Substances

  • Apolipoproteins E
  • Oligodeoxyribonucleotides
  • DNA