Laboratory of Genetic Skin Diseases, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
Hum Mutat. 2013 Jan;34(1):176-83. doi: 10.1002/humu.22203. Epub 2012 Oct 11.
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.
泛发性脓疱型银屑病(GPP)是一种罕见的、潜在危及生命的、侵袭性强的银屑病,其特征为突然发作,反复发作的皮肤炎症导致脓疱形成。家族性 GPP 已知是由 IL36RN 基因隐性遗传突变引起的,该基因编码白细胞介素 36 受体拮抗剂(IL-36Ra)。在本文中,我们对 14 例日本 GPP 患者的 IL36RN 基因进行了突变分析,并对其中 2 例患者进行了分析。一位患者为 c.115+6T>C 和 c.368C>G(p.Thr123Arg)复合杂合突变,而另一位患者携带 IL36RN 基因 c.28C>T(p.Arg10*)和 c.115+6T>C 复合杂合突变。使用患者皮肤的总 RNA 进行的表达研究表明,突变 c.115+6T>C 导致外显子 3 跳跃,导致移码和提前终止密码子(p.Arg10Argfs*1)。蛋白质结构分析表明,错义突变 p.Thr123Arg 导致 IL-36Ra 蛋白错误折叠和不稳定。体外细胞培养研究表明,p.Thr123Arg 突变体 IL-36Ra 蛋白表达受损,无法拮抗 IL-36 信号通路。我们的数据进一步强调了 IL36RN 在 GPP 发病机制中的关键作用。