Qian Guofeng, Yan Xiaoyi, Xuan Junli, Zheng Danfeng, He Zhiwen, Shen Jianguo
Department of Endocrinology, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, China.
Department of Cell Biology, College of Medicine, Zhejiang University, Hangzhou, China.
Front Cell Dev Biol. 2022 Aug 22;10:948350. doi: 10.3389/fcell.2022.948350. eCollection 2022.
Autoimmune polyendocrine syndrome type-1 (APS-1) is a rare inherited monogenic autoimmune disease characterized by the presence of at least two of three following major clinical features: chronic mucocutaneous candidiasis, hypoparathyroidism, and adrenal insufficiency. Mutations in autoimmune regulator (AIRE) gene have been found to contribute to APS-1. In the present study, we reported a 36-years-old male APS-1 patient who presented with hypoparathyroidism and Addison's disease. The proband underwent complete clinical examinations and mutation screening was performed by Sanger sequencing on AIRE gene. A novel homozygous mutation in exon 9 of the AIRE gene (c.1024C>T) was identified. Based on sequencing findings, HEK293T cell-based assays were conducted to analyze the subcellular localization and mutant transcript processing. Our results revealed that p.Q342X mutant localized in nuclear speckles and exerted a dominant-negative effect on wildtype AIRE function. We reported the c.1024C>T mutation of AIRE gene for the first time, which enriched the AIRE mutation database and contributed to further understanding of APS-1.
1型自身免疫性多内分泌腺综合征(APS-1)是一种罕见的遗传性单基因自身免疫性疾病,其特征是具有以下三大主要临床特征中的至少两种:慢性黏膜皮肤念珠菌病、甲状旁腺功能减退和肾上腺功能不全。已发现自身免疫调节因子(AIRE)基因突变与APS-1有关。在本研究中,我们报告了一名36岁的男性APS-1患者,他患有甲状旁腺功能减退和艾迪生病。先证者接受了全面的临床检查,并通过桑格测序对AIRE基因进行了突变筛查。在AIRE基因的第9外显子中鉴定出一个新的纯合突变(c.1024C>T)。基于测序结果,进行了基于HEK293T细胞的实验,以分析亚细胞定位和突变转录本加工。我们的结果显示,p.Q342X突变体定位于核斑,并对野生型AIRE功能发挥显性负效应。我们首次报道了AIRE基因的c.1024C>T突变,这丰富了AIRE突变数据库,并有助于进一步了解APS-1。