Mutations in GLDN, Encoding Gliomedin, a Critical Component of the Nodes of Ranvier, Are Responsible for Lethal Arthrogryposis

Am J Hum Genet. 2016 Oct 6;99(4):928-933. doi: 10.1016/j.ajhg.2016.07.021. Epub 2016 Sep 8.

Abstract

Arthrogryposis multiplex congenita (AMC) is a developmental condition characterized by multiple joint contractures resulting from reduced or absent fetal movements. Through linkage analysis, homozygosity mapping, and exome sequencing in four unrelated families affected by lethal AMC, we identified biallelic mutations in GLDN in the affected individuals. GLDN encodes gliomedin, a secreted cell adhesion molecule involved in the formation of the nodes of Ranvier. Transmission electron microscopy of the sciatic nerve from one of the affected individuals showed a marked lengthening defect of the nodes. The GLDN mutations found in the affected individuals abolish the cell surface localization of gliomedin and its interaction with its axonal partner, neurofascin-186 (NF186), in a cell-based assay. The axoglial contact between gliomedin and NF186 is essential for the initial clustering of Na+ channels at developing nodes. These results indicate a major role of gliomedin in node formation and the development of the peripheral nervous system in humans. These data indicate that mutations of GLDN or CNTNAP1 (MIM: 616286), encoding essential components of the nodes of Ranvier and paranodes, respectively, lead to inherited nodopathies, a distinct disease entity among peripheral neuropathies.

MeSH terms

  • Alleles
  • Arthrogryposis / genetics*
  • Axons / metabolism
  • Cell Adhesion Molecules / genetics
  • Cell Adhesion Molecules / metabolism
  • Cell Adhesion Molecules, Neuronal / genetics
  • Exome / genetics
  • Female
  • Fetal Death
  • Humans
  • Infant, Newborn
  • Male
  • Membrane Proteins / genetics*
  • Membrane Proteins / metabolism
  • Mutation*
  • Nerve Growth Factors / metabolism
  • Nerve Tissue Proteins / genetics*
  • Nerve Tissue Proteins / metabolism
  • Pedigree
  • Protein Binding / genetics
  • Ranvier's Nodes / metabolism*
  • Ranvier's Nodes / ultrastructure

Substances

  • CNTNAP1 protein, human
  • Cell Adhesion Molecules
  • Cell Adhesion Molecules, Neuronal
  • GLDN protein, human
  • Membrane Proteins
  • NFASC protein, human
  • Nerve Growth Factors
  • Nerve Tissue Proteins