A missense mutation in the proteolipid protein gene responsible for pelizaeus - merzbacher disease in a Japanese family

Akiko Iwaki, Tamaki Muramoto, Toru Iwaki, Hiroyasu Furumi, Maria L. Dario-deleon, Jun Tateishi, Yasuyuki Fukumaki

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Abstract

We investigated the proteolipid protein (PLP) gene of two boys in a Japanese family with Pelizaeus-Merzbacher disease (PMD), an X-linked neurologic disorder characterized by dysmyelination in the central nervous system (CNS). The patients showed similar clinical signs from birth and autopsy on the elder brother confirmed a connatal type of PMD. Direct sequencing of the PLP gene and PLP mRNAs from the brain of the PMD patient revealed a G to T transition in exon V of the PLP gene, which leads to a glycine to cystein substitution at residue 220. Allele-specific oligonucleotide hybridization revealed that this mutation was also present in his brother, but was absent in 100 X chromosomes of normal Japanese individuals. Northern blot analysis showed that the mRNA levels of PLP and myelin basic protein, two major myelin proteins produced by oligodendrocytes, were much reduced in the PMD brain, hence, there was a specific loss of oligodendrocytes. It seems likely that the substitution is responsible for PMD (connatal type) in this particular family and causes oligodendrocytes death in the CNS.

Original languageEnglish
Pages (from-to)19-22
Number of pages4
JournalHuman Molecular Genetics
Volume2
Issue number1
DOIs
Publication statusPublished - Jan 1 1993

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Pelizaeus-Merzbacher Disease
Proteolipids
Missense Mutation
Oligodendroglia
Proteins
Siblings
Central Nervous System
Myelin Proteins
Messenger RNA
Myelin Basic Protein
Protein Sequence Analysis
Brain
X Chromosome
Nervous System Diseases
Oligonucleotides
Northern Blotting
Glycine
Cause of Death
Autopsy
Exons

All Science Journal Classification (ASJC) codes

  • Molecular Biology
  • Genetics
  • Genetics(clinical)

Cite this

A missense mutation in the proteolipid protein gene responsible for pelizaeus - merzbacher disease in a Japanese family. / Iwaki, Akiko; Muramoto, Tamaki; Iwaki, Toru; Furumi, Hiroyasu; Dario-deleon, Maria L.; Tateishi, Jun; Fukumaki, Yasuyuki.

In: Human Molecular Genetics, Vol. 2, No. 1, 01.01.1993, p. 19-22.

Research output: Contribution to journalArticle

Iwaki, Akiko ; Muramoto, Tamaki ; Iwaki, Toru ; Furumi, Hiroyasu ; Dario-deleon, Maria L. ; Tateishi, Jun ; Fukumaki, Yasuyuki. / A missense mutation in the proteolipid protein gene responsible for pelizaeus - merzbacher disease in a Japanese family. In: Human Molecular Genetics. 1993 ; Vol. 2, No. 1. pp. 19-22.
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