Metabolism, Cell Surface Organization, and Disease

被引:375
作者
Dennis, James W. [1 ,2 ,3 ,4 ]
Nabi, Ivan R. [5 ]
Demetriou, Michael [6 ,7 ]
机构
[1] Mt Sinai Hosp, Samuel Lunenfeld Res Inst, Toronto, ON M5G 1X5, Canada
[2] Univ Toronto, Dept Mol Genet, Toronto, ON M5S 1A8, Canada
[3] Univ Toronto, Dept Lab Med, Toronto, ON M5S 1A8, Canada
[4] Univ Toronto, Dept Pathol, Toronto, ON M5S 1A8, Canada
[5] Univ British Columbia, Inst Life Sci, Dept Cellular & Physiol Sci, Vancouver, BC V6T 1Z3, Canada
[6] Univ Calif Irvine, Inst Immunol, Dept Neurol, Irvine, CA 92697 USA
[7] Univ Calif Irvine, Inst Immunol, Dept Microbiol & Mol Genet, Irvine, CA 92697 USA
关键词
N-ACETYLGLUCOSAMINYLTRANSFERASE-V; LINKED OLIGOSACCHARIDES; CAENORHABDITIS-ELEGANS; PROTEIN GLYCOSYLATION; GLCNAC-TRANSFERASE; ACID BIOSYNTHESIS; GENE-EXPRESSION; GLYCAN; GROWTH; RECEPTOR;
D O I
10.1016/j.cell.2009.12.008
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
Genetic information flows from DNA to macromolecular structures-the dominant force in the molecular organization of life. However, recent work suggests that metabolite availability to the hexosamine and Golgi N-glycosylation pathways exerts control over the assembly of macromolecular complexes on the cell surface and, in this capacity, acts upstream of signaling and gene expression. The structure and number of N-glycans per protein molecule cooperate to regulate lectin binding and thereby the distribution of glycoproteins at the cell surface. Congenital disorders of glycosylation provide insight as extreme hypomorphisms, whereas milder deficiencies may encompass many common chronic conditions, including autoimmunity, metabolic syndrome, and aging. © 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:1229 / 1241
页数:13
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