Nakashima Mitsuko, Kashii Hirofumi, Murakami Yoshiko, Kato Mitsuhiro, Tsurusaki Yoshinori, Miyake Noriko, Kubota Masaya, Kinoshita Taroh, Saitsu Hirotomo, Matsumoto Naomichi
Department of Human Genetics, Yokohama City University Graduate School of Medicine, 3-9 Fukuura, Kanazawa-ku, Yokohama, 236-0004, Japan.
Neurogenetics. 2014 Aug;15(3):193-200. doi: 10.1007/s10048-014-0408-y. Epub 2014 Jun 8.
Recessive mutations in genes of the glycosylphosphatidylinositol (GPI)-anchor synthesis pathway have been demonstrated as causative of GPI deficiency disorders associated with intellectual disability, seizures, and diverse congenital anomalies. We performed whole exome sequencing in a patient with progressive encephalopathies and multiple dysmorphism with hypophosphatasia and identified novel compound heterozygous mutations, c.250G>T (p. Glu84*) and c.1342C>T (p. Arg488Trp), in PIGT encoding a subunit of the GPI transamidase complex. The surface expression of GPI-anchored proteins (GPI-APs) on patient granulocytes was lower than that of healthy controls. Transfection of the Arg488Trp mutant PIGT construct, but not the Glu84* mutant, into PIGT-deficient cells partially restored the expression of GPI-APs DAF and CD59. These results indicate that PIGT mutations caused neurological impairment and multiple congenital anomalies in this patient.
糖基磷脂酰肌醇(GPI)锚定合成途径基因中的隐性突变已被证实是导致与智力残疾、癫痫和多种先天性异常相关的GPI缺乏症的原因。我们对一名患有进行性脑病、多种发育异常并伴有低磷酸酯酶症的患者进行了全外显子组测序,在编码GPI转酰胺酶复合体一个亚基的PIGT基因中鉴定出了新的复合杂合突变,即c.250G>T(p.Glu84*)和c.1342C>T(p.Arg488Trp)。患者粒细胞上GPI锚定蛋白(GPI-APs)的表面表达低于健康对照。将Arg488Trp突变体PIGT构建体而非Glu84*突变体转染到PIGT缺陷细胞中,可部分恢复GPI-APs DAF和CD59的表达。这些结果表明,PIGT突变导致了该患者的神经功能损害和多种先天性异常。