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Stepwise assembly of the lipid-linked oligosaccharide in the endoplasmic reticulum of Saccharomyces cerevisiae: identification of the ALG9 gene encoding a putative mannosyl transferase.

机译:在酿酒酵母的内质网中脂质连接的寡糖的逐步组装:编码假定的甘露糖基转移酶的ALG9基因的鉴定。

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摘要

The core oligosaccharide Glc3Man9GlcNAc2 is assembled at the membrane of the endoplasmic reticulum on the lipid carrier dolichyl pyrophosphate and transferred to selected asparagine residues of nascent polypeptide chains. This transfer is catalyzed by the oligosaccharyl transferase complex. Based on the synthetic phenotype of the oligosaccharyl transferase mutation wbp1 in combination with a deficiency in the assembly pathway of the oligosaccharide in Saccharomyces cerevisiae, we have identified the novel ALG9 gene. We conclude that this locus encodes a putative mannosyl transferase because deletion of the gene led to accumulation of lipid-linked Man6GlcNAc2 in vivo and to hypoglycosylation of secreted proteins. Using an approach combining genetic and biochemical techniques, we show that the assembly of the lipid-linked core oligosaccharide in the lumen of the endoplasmic reticulum occurs in a stepwise fashion.
机译:核心寡糖Glc3Man9GlcNAc2组装在内质网膜上的脂质载体焦磷酸焦磷酸中,并转移到新生多肽链的选定天冬酰胺残基上。该转移是由寡糖基转移酶复合物催化的。基于寡糖基转移酶突变wbp1的综合表型与酿酒酵母中寡糖装配途径的缺陷相结合,我们已经确定了新的ALG9基因。我们得出的结论是,该基因座编码一个假定的甘露糖基转移酶,因为该基因的缺失导致体内脂质连接的Man6GlcNAc2积累和分泌蛋白的低糖基化。使用结合遗传和生化技术的方法,我们显示在内质网腔中脂质连接的核心寡糖的组装以逐步的方式发生。

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