Linkage of a new mutation in the proteolipid protein (PLP) gene to Pelizaeus-Merzbacher disease (PMD) in a large Finnish kindred

Am J Hum Genet. 1993 Jun;52(6):1053-6.

Abstract

The purpose of this study was to confirm linkage of the proteolipid protein gene (PLP) and Pelizaeus-Merzbacher disease (PMD). A T-->A transversion in nucleotide pair 35 of exon 4 of PLP was found in a large Finnish kindred with PMD. This mutation results in the substitution Val165-->Glu165. We used a combination of single-strand conformational polymorphism and PCR primer extension to determine the presence or absence of the point mutation in family members. A lod score of 2.6 (theta = 0) was found for linkage of the gene and the disease. We examined 101 unrelated X chromosomes and found none with the transversion. This is the second report of linkage of PMD to a missense mutation in PLP. These findings support the hypothesis that PMD in this family is a result of the missense mutation present in exon 4 of PLP.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • DNA Mutational Analysis
  • DNA, Single-Stranded
  • Diffuse Cerebral Sclerosis of Schilder / genetics*
  • Female
  • Finland
  • Genetic Linkage*
  • Humans
  • Male
  • Molecular Sequence Data
  • Myelin Proteins / genetics*
  • Myelin Proteolipid Protein
  • Pedigree
  • Point Mutation*
  • Polymorphism, Genetic
  • X Chromosome

Substances

  • DNA, Single-Stranded
  • Myelin Proteins
  • Myelin Proteolipid Protein