Bathing suit ichthyosis is caused by transglutaminase-1 deficiency: evidence for a temperature-sensitive phenotype

Hum Mol Genet. 2006 Nov 1;15(21):3083-97. doi: 10.1093/hmg/ddl249. Epub 2006 Sep 12.

Abstract

Bathing suit ichthyosis (BSI) is a striking and unique clinical form of autosomal recessive congenital ichthyosis characterized by pronounced scaling on the bathing suit areas but sparing of the extremities and the central face. Here we report on a series of 10 BSI patients. Our genetic, ultrastructural and biochemical investigations show that BSI is caused by transglutaminase-1 (TGase-1) deficiency. Altogether, we identified 13 mutations in TGM1-among them seven novel missense mutations and one novel nonsense mutation. Structural modeling for the Tyr276Asn mutation reveals that the residue is buried in the hydrophobic interior of the enzyme and that the hydroxyl side chain of Tyr276 is exposed to solvent in a cavity of the enzyme. Cryosections of healthy skin areas demonstrated an almost normal TGase activity, in contrast to the affected BSI skin, which only showed a cytoplasmic and clearly reduced TGase-1 activity. The distribution of TGase-1 substrates in the epidermis of affected skin corresponded to the situation in TGase-1 deficiency. Interestingly, the expression of TGase-3 and cathepsin D was reduced. Digital thermography validated a striking correlation between warmer body areas and presence of scaling in patients suggesting a decisive influence of the skin temperature. In situ TGase testing in skin of BSI patients demonstrated a marked decrease of enzyme activity when the temperature was increased from 25 to 37 degrees C. We conclude that BSI is caused by TGase-1 deficiency and suggest that it is a temperature-sensitive phenotype.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • Chromosome Mapping
  • Codon, Nonsense
  • Female
  • Humans
  • Ichthyosis / enzymology
  • Ichthyosis / genetics*
  • Ichthyosis / pathology
  • Infant
  • Male
  • Models, Molecular
  • Mutation, Missense
  • Phenotype
  • Sequence Analysis, DNA
  • Skin / enzymology
  • Skin / pathology
  • Temperature
  • Transglutaminases / chemistry
  • Transglutaminases / deficiency*
  • Transglutaminases / genetics*
  • Transglutaminases / metabolism

Substances

  • Codon, Nonsense
  • Transglutaminases
  • transglutaminase 1