Cloning and characterization of the ALG3 gene of Saccharomyces cerevisiae

被引:105
作者
Aebi, M
Gassenhuber, J
Domdey, H
Heesen, ST
机构
[1] ETH ZURICH, INST MIKROBIOL, CH-8092 ZURICH, SWITZERLAND
[2] UNIV MUNICH, GENZENTRUM, INST BIOCHEM, D-81375 MUNICH, GERMANY
关键词
lipid-linked oligosaccharide; N-glycosylation; synthetic lethality;
D O I
10.1093/glycob/6.4.439
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The Saccharomyces cerevisiae alg3-1 mutant is described as defective in the biosynthesis of dolichol-linked oligosaccharides (Huffaker and Robbins, Proc, Nad Acad, Sci, USA, 80, 7466-7470, 1983), Man(5)GlcNAc(2)-PP-Dol accumulates in alg3 cells and Endo H resistant carbohydrates are transferred to protein by the oligosaccharyltransferase complex. In this study, we describe the cloning of the ALG3 locus by complementation of the temperature sensitive growth defect of the alg3 stt3 double mutant. The isolated ALG3 gene complements both the defect in the biosynthesis of lipid-linked oligosaccharides of the alg3-mutant and the under-glycosylation of secretory proteins, The inactivation of the nonessential ALG3 gene results in the accumulation of lipid-linked Man(5)GlcNAc(2) and protein-bound carbohydrates which are completely Endo H resistant, The ALG3 locus encodes a potential ER-transmembrane protein of 458 amino acids (53 kDa) with a C-terminal KKXX-retrieval sequence.
引用
收藏
页码:439 / 444
页数:6
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