Burda P, Borsig L, de Rijk-van Andel J, Wevers R, Jaeken J, Carchon H, Berger E G, Aebi M
Microbiology Institute, ETH Zurich, ETH Zentrum, CH-8092 Zurich, Switzerland.
J Clin Invest. 1998 Aug 15;102(4):647-52. doi: 10.1172/JCI2266.
Carbohydrate-deficient glycoprotein syndromes (CDGS) type I are a group of genetic diseases characterized by a deficiency of N-linked protein glycosylation in the endoplasmic reticulum. The majority of these CDGS patients have phosphomannomutase (PMM) deficiency (type A). This enzyme is required for the synthesis of GDP-mannose, one of the substrates in the biosynthesis of the dolichol-linked oligosaccharide Glc3Man9GlcNAc2. This oligosaccharide serves as the donor substrate in the N-linked glycosylation process. We report on the biochemical characterization of a novel CDGS type I in fibroblasts of four related patients with normal PMM activity but a strongly reduced ability to synthesize glucosylated dolichol-linked oligosaccharide leading to accumulation of dolichol-linked Man9GlcNAc2. This deficiency in the synthesis of dolichol-linked Glc3Man9GlcNAc2 oligosaccharide explains the hypoglycosylation of serum proteins in these patients, because nonglucosylated oligosaccharides are suboptimal substrates in the protein glycosylation process, catalyzed by the oligosaccharyltransferase complex. Accordingly, the efficiency of N-linked protein glycosylation was found to be reduced in fibroblasts from these patients.
I型碳水化合物缺乏糖蛋白综合征(CDGS)是一组遗传性疾病,其特征是内质网中N-连接蛋白糖基化缺乏。这些CDGS患者大多数存在磷酸甘露糖变位酶(PMM)缺乏(A型)。该酶是合成GDP-甘露糖所必需的,而GDP-甘露糖是多萜醇连接的寡糖Glc3Man9GlcNAc2生物合成中的底物之一。这种寡糖在N-连接糖基化过程中作为供体底物。我们报道了在四名相关患者的成纤维细胞中一种新型I型CDGS的生化特征,这些患者PMM活性正常,但合成糖基化多萜醇连接寡糖的能力大幅降低,导致多萜醇连接的Man9GlcNAc2积累。多萜醇连接的Glc3Man9GlcNAc2寡糖合成的这种缺陷解释了这些患者血清蛋白的低糖基化,因为非糖基化寡糖在寡糖基转移酶复合物催化的蛋白质糖基化过程中是次优底物。因此,发现这些患者成纤维细胞中N-连接蛋白糖基化的效率降低。