A novel glutamic acid to aspartic acid mutation near the end of the 2B rod domain in the keratin 1 chain in epidermolytic hyperkeratosis

J Invest Dermatol. 1999 Mar;112(3):376-9. doi: 10.1038/sj.jid.5600439.

Abstract

We report a mutation in a mild case of epidermolytic hyperkeratosis that results in a glutamic acid to aspartic acid substitution in a novel location, codon 477 or position 106 of the 2B rod domain of the keratin 1 chain. This residue has been conserved in all intermediate filament chains and lies near the beginning of the highly conserved helix termination sequence and just prior to the predicted molecular overlap region. Keratin filaments assembled in vitro from chains bearing this substitution are abnormal, indicating that the glutamic acid residue is critically involved in ionic interactions in intermediate levels of filament structure.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Substitution / genetics*
  • Aspartic Acid / genetics*
  • Base Sequence / genetics
  • Female
  • Glutamic Acid / genetics*
  • Humans
  • Hyperkeratosis, Epidermolytic / genetics*
  • Intermediate Filaments / metabolism
  • Intermediate Filaments / ultrastructure
  • Keratins / genetics*
  • Male
  • Pedigree

Substances

  • Aspartic Acid
  • Glutamic Acid
  • Keratins