Burda P, te Heesen S, Brachat A, Wach A, Düsterhöft A, Aebi M
Mikrobiologisches Institut, ETH Zürich, Switzerland.
Proc Natl Acad Sci U S A. 1996 Jul 9;93(14):7160-5. doi: 10.1073/pnas.93.14.7160.
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.
核心寡糖Glc3Man9GlcNAc2在内质网膜上由脂质载体焦磷酸多萜醇组装而成,并转移至新生多肽链上特定的天冬酰胺残基。这种转移由寡糖基转移酶复合体催化。基于酿酒酵母中寡糖基转移酶突变体wbp1的合成表型以及寡糖组装途径的缺陷,我们鉴定出了新的ALG9基因。我们得出结论,该基因座编码一种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积累以及分泌蛋白的低糖基化。通过结合遗传和生化技术的方法,我们表明内质网腔中脂质连接的核心寡糖的组装是逐步进行的。