PLoS ONE (Jan 2012)

Genetic variation in the epidermal transglutaminase genes is not associated with atopic dermatitis.

  • Agne Liedén,
  • Mårten C G Winge,
  • Annika Sääf,
  • Ingrid Kockum,
  • Elisabeth Ekelund,
  • Elke Rodriguez,
  • Regina Fölster-Holst,
  • Andre Franke,
  • Thomas Illig,
  • Maria Tengvall-Linder,
  • Hansjörg Baurecht,
  • Stephan Weidinger,
  • Carl-Fredrik Wahlgren,
  • Magnus Nordenskjöld,
  • Maria Bradley

DOI
https://doi.org/10.1371/journal.pone.0049694
Journal volume & issue
Vol. 7, no. 11
p. e49694

Abstract

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BackgroundAtopic dermatitis (AD) is a common chronic inflammatory skin disorder where epidermal barrier dysfunction is a major factor in the pathogenesis. The identification of AD susceptibility genes related to barrier dysfunction is therefore of importance. The epidermal transglutaminases (TGM1, TGM3 and TGM5) encodes essential cross-linking enzymes in the epidermis.ObjectiveTo determine whether genetic variability in the epidermal transglutaminases contributes to AD susceptibility.MethodsForty-seven single nucleotide polymorphisms (SNPs) in the TGM1, TGM3 and TGM5 gene region were tested for genetic association with AD, independently and in relation to FLG genotype, using a pedigree disequilibrium test (PDT) in a Swedish material consisting of 1753 individuals from 539 families. In addition, a German case-control material, consisting of 533 AD cases and 1996 controls, was used for in silico analysis of the epidermal TGM regions. Gene expression of the TGM1, TGM3 and TGM5 gene was investigated by relative quantification with Real Time PCR (qRT-PCR). Immunohistochemical (IHC) analysis was performed to detect TG1, TG3 and TG5 protein expression in the skin of patients and healthy controls.ResultsPDT analysis identified a significant association between the TGM1 SNP rs941505 and AD with allergen-specific IgE in the Swedish AD family material. However, the association was not replicated in the German case-control material. No significant association was detected for analyzed SNPs in relation to FLG genotype. TG1, TG3 and TG5 protein expression was detected in AD skin and a significantly increased TGM3 mRNA expression was observed in lesional skin by qRT-PCR.ConclusionAlthough TGM1 and TGM3 may be differentially expressed in AD skin, the results from the genetic analysis suggest that genetic variation in the epidermal transglutaminases is not an important factor in AD susceptibility.