A novel insertional mutation in loricrin in Vohwinkel's Keratoderma

J Invest Dermatol. 1998 Oct;111(4):702-4. doi: 10.1046/j.1523-1747.1998.00343.x.

Abstract

A mutation in the gene encoding loricrin has recently been reported in a subset of patients with Vohwinkel's Keratoderma manifesting an associated ichthyosiform dermatosis. We have studied a further kindred with this clinical phenotype. Microsatellite marker analysis was consistent with linkage to chromosome 1q21 and direct sequencing of loricrin identified a heterozygous mutation with an insertion of a T residue at codon 209. This mutation is predicted to produce a mutant protein with a frameshift of its terminal 107 amino acids and to be 22 amino acids longer than the wild-type protein due to a delayed termination codon. The only previously reported mutation is a G insertion producing a frameshift after codon 231. The novel mutation we report is likely to have a similar functional effect on cornified envelope formation, with disturbance of transglutaminase-mediated cross-linking of envelope components, and serves to confirm the predicted role of insertional mutations in Vohwinkel's Keratoderma associated with ichthyosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Chromosomes, Human, Pair 1 / genetics
  • Family Health
  • Female
  • Genetic Linkage
  • Humans
  • Ichthyosis / genetics*
  • Keratoderma, Palmoplantar / pathology
  • Male
  • Membrane Proteins / genetics*
  • Molecular Sequence Data
  • Mutagenesis, Insertional
  • Pedigree
  • Phenotype

Substances

  • Membrane Proteins
  • loricrin