首页> 美国卫生研究院文献>Molecular and Cellular Biology >Control of carbohydrate processing: increased beta-16 branching in N-linked carbohydrates of Lec9 CHO mutants appears to arise from a defect in oligosaccharide-dolichol biosynthesis.
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Control of carbohydrate processing: increased beta-16 branching in N-linked carbohydrates of Lec9 CHO mutants appears to arise from a defect in oligosaccharide-dolichol biosynthesis.

机译:碳水化合物加工的控制:Lec9 CHO突变体的N-连接碳水化合物中β-16分支的增加似乎是由于寡糖-乙醇化学合成的缺陷引起的。

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摘要

A correlation between increased beta-1,6 branching of N-linked carbohydrates and the ability of a cell to metastasize or to form a tumor has been observed in several experimental models. Lec9 Chinese hamster ovary (CHO) mutants exhibit a drastic reduction in tumorigenicity in nude mice, and this phenotype directly correlates with their ability to attach an increased proportion of beta-1,6-branched carbohydrates to the G glycoprotein of vesicular stomatitis virus (J. Ripka, S. Shin, and P. Stanley, Mol. Cell. Biol. 6:1268-1275, 1986). In this paper we provide evidence that cellular carbohydrates from Lec9 cells also contain an increased proportion of beta-1,6-branched carbohydrates, although they do not possess significantly increased activity of the beta-1,6 branching enzyme (GlcNAc-transferase V). Biosynthetic labeling experiments show that a substantial degree of underglycosylation occurs in Lec9 cells and that this affects several classes of glycoproteins. Lec9 cells synthesize ca. 40-fold less Glc3Man9GlcNAc2-P-P-lipid and ca. 2-fold less Man5GlcNAc2-P-P-lipid than parental cells do. In addition, Lec9 cells possess ca. fivefold less protein-bound oligosaccharide intermediates, and one major species is resistant to release by endo-beta-N-acetylglucosaminidase H (endo H). Membranes of Lec9 cells exhibit normal mannosylphosphoryldolichol synthase, glucosylphosphoryldolichol synthase, and N-acetylglucosaminylphosphate transferase activities in the presence of exogenous dolichyl phosphate. However, in the absence of exogenous dolichyl phosphate, mannosylphosphoryldolichol synthase and glucosylphosphoryldolichol synthase activities are reduced in membranes of Lec9 cells, indicating that membranes of Lec9 cells are deficient in lipid phosphate. This was confirmed by analysis of lipids labeled by [3H]mevalonate, which showed that Lec9 cells have less lipid phosphate than parental CHO cells. Mechanisms by which a defect in the synthesis of dolichol-oligosaccharides might alter the degree of beta-1,6 branching in N-linked carbohydrates are discussed.
机译:在几个实验模型中已观察到N-连接碳水化合物的β-1,6分支增加与细胞转移或形成肿瘤的能力之间的相关性。 Lec9中国仓鼠卵巢(CHO)突变体在裸鼠中显着降低了致瘤性,这种表型与它们将增加比例的β-1,6-分支碳水化合物与水泡性口腔炎病毒的G糖蛋白附着的能力直接相关(J (Ripka,S.Shin,和P.Stanley,Mol.Cell.Biol.6:1268-1275,1986)。在本文中,我们提供了证据,表明来自Lec9细胞的细胞碳水化合物也含有增加比例的β-1,6-支链碳水化合物,尽管它们不具有显着增加的β-1,6分支酶(GlcNAc-转移酶V)活性。 。生物合成标记实验表明,Lec9细胞中发生了很大程度的糖基化不足,这影响了几类糖蛋白。 Lec9细胞合成ca。少40倍的Glc3Man9GlcNAc2-P-P-脂质和ca. Man5GlcNAc2-P-P-脂质比亲代细胞少2倍。此外,Lec9细胞拥有约。蛋白质结合的寡糖中间体的含量减少了五倍,并且一个主要种类对内切β-N-乙酰氨基葡萄糖苷酶H(内切H)具有抗释放性。在外源性磷酸二氢磷酸酯存在下,Lec9细胞的膜表现出正常的甘露糖基磷酸亚砜基合酶,葡糖基磷酸亚砜基合酶和N-乙酰基氨基葡萄糖磷酸酯基转移酶活性。但是,在不存在外源性二磷酸二氢磷酸酯的情况下,Lec9细胞的膜中的甘露糖基磷酸二水醇合酶和葡萄糖基磷酸二水醇合酶的活性降低,表明Lec9细胞的膜中缺乏磷酸脂。通过用[3H]甲羟戊酸标记的脂质的分析证实了这一点,这表明Lec9细胞比亲代CHO细胞具有更少的脂质磷酸。讨论了通过机制合成多聚醇-寡糖的缺陷可能会改变N-连接碳水化合物中β-1,6支化度的机制。

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