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UDP-GlcNAc:糖蛋白 N-乙酰氨基葡萄糖-1-磷酸转移酶介导甲基磷酸甘露糖残基在盘基网柄菌糖蛋白高甘露糖寡糖上形成的初始步骤。

UDP-GlcNAc:Glycoprotein N-acetylglucosamine-1-phosphotransferase mediates the initial step in the formation of the methylphosphomannosyl residues on the high mannose oligosaccharides of Dictyostelium discoideum glycoproteins.

机构信息

Department of Internal Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.

出版信息

Biochem Biophys Res Commun. 2010 Mar 19;393(4):678-81. doi: 10.1016/j.bbrc.2010.02.055. Epub 2010 Feb 17.

Abstract

The Dictyostelium discoideum gene gpt1 encodes a protein XP_638036 with sequence similarity to the alpha/beta subunits of mammalian UDP-GlcNAc:Glycoprotein N-acetylglucosamine-1-phosphotransferase. We now demonstrate that extracts of D. discoideum clones with mutations in this gene transfer GlcNAc-P from UDP-GlcNAc to mannose residues at less than 5% the wild type value. Further, the lysosomal hydrolases of these mutant clones fail to bind to a cation-independent mannose 6-phosphate receptor affinity column, indicating a lack of methylphosphomannosyl residues on the high mannose oligosaccharides of these proteins. We conclude that the gpt1 gene product catalyzes the initial step in the formation of methylphosphomannosyl residues on D. discoideum lysosomal hydrolases.

摘要

盘基网柄菌基因 gpt1 编码一种蛋白 XP_638036,与哺乳动物 UDP-GlcNAc:糖蛋白 N-乙酰氨基葡萄糖-1-磷酸转移酶的α/β亚基具有序列相似性。我们现在证明,该基因发生突变的盘基网柄菌克隆提取物将 GlcNAc-P 从 UDP-GlcNAc 转移到甘露糖残基的速率不到野生型的 5%。此外,这些突变克隆的溶酶体水解酶不能与阳离子非依赖性甘露糖 6-磷酸受体亲和柱结合,表明这些蛋白的高甘露糖寡糖上缺乏甲基磷酸甘露糖残基。我们的结论是,gpt1 基因产物催化盘基网柄菌溶酶体水解酶上甲基磷酸甘露糖残基形成的第一步。

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