Structure, function and pathology of O-mannosyl glycans

被引:44
作者
Endo, T [1 ]
机构
[1] Tokyo Metropolitan Inst Gerontol, Fdn Res Aging & Promot Human Welf, Glycobiol Res Grp, Itabashi Ku, Tokyo 1730015, Japan
关键词
O-mannosylation; congenital muscular dystrophy; dystroglycan; glycosyltransferase;
D O I
10.1023/B:GLYC.0000043740.26062.2c
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
Animal cells contain many glycoproteins, i.e., proteins with covalently liked sugar chains. The major glycans of glycoproteins can be classified into two groups, N-glycans and O-glycans, according to their glycan-peptide linkage regions. Development of sensitive methods for the analyses of glycan structures have revealed a new type of glycosidic linkage to the peptide portion, the O-mannosyl linkage, in mammals, which used to be considered specific to yeast. O-Mannosylation is present in a limited number of glycoproteins of brain, nerve, and skeletal muscle. Recently O-mannosylation has been shown to be important in muscle and brain development. Glycobiology of O-mannosyl glycans is expected to produce remarkable advances in the understanding and treatment of congenital muscular dystrophies. In this article, I describe the structure, biosynthesis, and pathology of O-mannosyl glycans.
引用
收藏
页码:3 / 7
页数:5
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