1. Academic Validation
  2. Mutation analysis of the IL36RN gene in 14 Japanese patients with generalized pustular psoriasis

Mutation analysis of the IL36RN gene in 14 Japanese patients with generalized pustular psoriasis

  • Hum Mutat. 2013 Jan;34(1):176-83. doi: 10.1002/humu.22203.
Muhammad Farooq 1 Hiroyuki Nakai Atsushi Fujimoto Hiroki Fujikawa Asako Matsuyama Naoyuki Kariya Atsuko Aizawa Hiroshi Fujiwara Masaaki Ito Yutaka Shimomura
Affiliations

Affiliation

  • 1 Laboratory of Genetic Skin Diseases, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Abstract

Generalized pustular psoriasis (GPP) is a rare, potentially life threatening, and aggressive form of psoriasis, which is characterized by sudden onset with repeated episodic skin inflammation leading to pustule formation. Familial GPP is known to be caused by recessively inherited mutations in the IL36RN gene, which encodes interleukin 36 receptor antagonist (IL-36RA). In this article, we performed mutation analysis of the IL36RN gene in 14 Japanese patients with GPP, and identified mutations in two of these patients analyzed. One patient was compound heterozygous for mutations c.115+6T>C and c.368C>G (p.Thr123Arg), whereas the other carried compound heterozygous mutations c.28C>T (p.Arg10*) and c.115+6T>C in the IL36RN gene. Expression studies using total RNA from the patients' skin revealed that the mutation c.115+6T>C resulted in skipping of exon 3, leading to a frameshift and a premature termination codon (p.Arg10Argfs*1). The protein structure analysis suggested that the missense mutation p.Thr123Arg caused misfolding and instability of IL-36RA protein. In vitro studies in cultured cells showed impaired expression of the p.Thr123Arg mutant IL-36RA protein, which failed to antagonize the IL-36 signaling pathway. Our data further underscore the critical role of IL36RN in pathogenesis of GPP.

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