Kinoshita T, Ohishi K, Takeda J
Department of Immunoregulation, Research Institute for Microbial Diseases, Osaka University, Suita.
J Biochem. 1997 Aug;122(2):251-7. doi: 10.1093/oxfordjournals.jbchem.a021746.
Protein GPI anchors are ubiquitous in eukaryotic cells. More than 50 mammalian proteins are anchored to the membrane via GPI. GPI anchoring is a posttranslational modification occurring in the endoplasmic reticulum where preassembled GPI anchor precursors are transferred to proteins bearing a C-terminal GPI signal sequence. The GPI anchor precursors are synthesized in the endoplasmic reticulum by sequential addition of sugar and other components to phosphatidylinositol. More than ten genes participate in this biosynthetic pathway, eleven of the mammalian genes having been cloned by means of complementation of mutant cells that are defective in this pathway or based on sequence homology to previously cloned yeast counterparts. A somatic mutation in one of those genes, PIG-A, involved in the first reaction step, is responsible for the hemolytic disease, paroxysmal nocturnal hemoglobinuria.
糖基磷脂酰肌醇(GPI)锚定蛋白在真核细胞中普遍存在。超过50种哺乳动物蛋白通过GPI锚定在细胞膜上。GPI锚定是一种发生在内质网的翻译后修饰,在此过程中,预先组装好的GPI锚定前体被转移到带有C端GPI信号序列的蛋白质上。GPI锚定前体在内质网中通过将糖和其他成分依次添加到磷脂酰肌醇上而合成。十多个基因参与了这一生物合成途径,其中11个哺乳动物基因已通过对该途径有缺陷的突变细胞进行互补克隆,或基于与先前克隆的酵母对应基因的序列同源性克隆得到。参与第一步反应的其中一个基因PIG-A发生体细胞突变,是导致溶血性疾病阵发性夜间血红蛋白尿的原因。