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  • 标题:A unique molecular chaperone Cosmc required for activity of the mammalian core 1 β3-galactosyltransferase
  • 本地全文:下载
  • 作者:Tongzhong Ju ; Richard D. Cummings
  • 期刊名称:Proceedings of the National Academy of Sciences
  • 印刷版ISSN:0027-8424
  • 电子版ISSN:1091-6490
  • 出版年度:2002
  • 卷号:99
  • 期号:26
  • 页码:16613-16618
  • DOI:10.1073/pnas.262438199
  • 语种:English
  • 出版社:The National Academy of Sciences of the United States of America
  • 摘要:Human core 1 {beta}3-galactosyltransferase (C1{beta}3Gal-T) generates the core 1 O-glycan Gal{beta}1-3GalNAc1-Ser/Thr (T antigen), which is a precursor for many extended O-glycans in animal glycoproteins. We report here that C1{beta}3Gal-T activity requires expression of a molecular chaperone designated Cosmc (core 1 {beta}3-Gal-T-specific molecular chaperone). The human Cosmc gene is X-linked (Xq23), and its cDNA predicts a 318-aa transmembrane protein ({approx}36.4 kDa) with type II membrane topology. The human lymphoblastoid T cell line Jurkat, which lacks C1{beta}3Gal-T activity and expresses the Tn antigen GalNAc1-Ser/Thr, contains a normal gene and mRNA encoding C1{beta}3Gal-T, but contains a mutated Cosmc with a deletion introducing a premature stop codon. Expression of Cosmc cDNA in Jurkat cells restored C1{beta}3Gal-T activity and T antigen expression. Without Cosmc, the C1{beta}3Gal-T is targeted to proteasomes. Expression of active C1{beta}3Gal-T in Hi-5 insect cells requires coexpression of Cosmc. Overexpression of active C1{beta}3Gal-T in mammalian cell lines also requires coexpression of Cosmc, indicating that endogenous Cosmc may be limiting. A small portion of C1{beta}3Gal-T copurifies with Cosmc from cell extracts, demonstrating physical association of the proteins. These results indicate that Cosmc acts as a specific molecular chaperone in assisting the folding/stability of C1{beta}3Gal-T. The identification of Cosmc, a uniquely specific molecular chaperone required for a glycosyltransferase expression in mammalian cells, may shed light on the molecular basis of acquired human diseases involving altered O-glycosylation, such as IgA nephropathy, Tn syndrome, Henoch-Schonlein purpura, and malignant transformation, all of which are associated with a deficiency of C1{beta}3Gal-T activity.
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