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Cosmc和T-合酶在黏蛋白型O-聚糖合成中的重要作用及其与人类疾病的相关性 被引量:4

The key role of Cosmc and T-synthase in mucin-type O-glycan biosynthesisimplications in human diseases
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摘要 从核心1结构(Galβ1,3GalNAcα1-O-Ser/Thr,core 1 structure,T antigen)中衍生出来的黏蛋白型O-聚糖在很多生理过程中发挥重要的生物学功能。T-合酶(core 1β3-galactosyltransferase,T-synthase)是合成核心1结构的唯一糖基转移酶,它主要的功能是将半乳糖(Galactose)添加到GalNAcα1-Ser/Thr(Tn抗原)糖链上。但是在人体和其他脊椎动物中有活性的T-合酶的形成需要一个重要的伴侣分子Cosmc;Cosmc功能丧失将直接导致T-合酶失活,其结果是机体细胞只能合成Tn抗原以及唾液酰化Tn(sialylTn,STn,Neu5Acα2,6GalNAcα1-O-Ser/Thr)。综述目前对T-合酶和Cosmc的研究以及在人类疾病(如异常O-聚糖表达相关的Tn综合征、IgA肾病和肿瘤)发生发展中的作用。 Mucin type O-glycans, primarily derived from the core 1 structure, play pivotal functions in many biological processes. The T-synthase (core 1 [33-galactosyltransferase) is the key enzyme responsible for synthesizing the core l O-glycan GalD 1,3GalNAcctl-Ser/Thr (T antigen) through addition of Gal to GalNAcct 1-Ser/ Thr (Tn antigen). Interestingly, formation of active T-synthase in human and other vertebrates requires a specific molecular chaperone, Cosmc. Dysfunction of Cosmc results in an inactive T-synthase leading to expression of the Tn antigen and its sialylated version, sialylTn (STn, Neu5Acct2,6GalNAcul-Ser/Thr). This review summarizes the current understanding of the T-synthase and Cosmc regarding their biochemistry and biology, as well as their roles in human diseases, such as Tn syndrome, IgA nephropathy, and human tumors, which are associated with expression of abnormal O-glycans.
出处 《生命科学》 CSCD 北大核心 2011年第7期630-642,共13页 Chinese Bulletin of Life Sciences
基金 National Institutes of Health Grants(RO1 DK80876 RO1 GM068559)
关键词 O-聚糖 T-合酶 分子伴侣 Cosmc Tn抗原 O-glycan T-synthase molecular chaperone Cosmc Tn antigen
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  • 1Varki, A. Biological roles of oligosaccharides: all of the theories are correct. Glycobiology, 1993, 3(2): 97-130.
  • 2Yago T, Leppanen A, Carlyon JA, et al. Structurally distinct requirements for binding of P-selectin glycoprotein ligand-1 and sialyl Lewis x to Anaplasma phagocytophilum and P-selectin. J Biol Chem, 2003, 278(39): 37987-97.
  • 3Blanchard B, Nurisso A, Hollville E, et al. Structural basis of the preferential binding for globo-series glycosphingo- lipids displayed by Pseudomonas aeruginosa lectin I. JMol Biol,2008,383(4):837-53.
  • 4Chung MC, Wines BD, Baker H, et al. The crystal structure of staphylococcal superantigen-like protein 11 in complex with sialyl Lewis X reveals the mechanism for cell binding and immune inhibition. Mol Microbiol, 2007, 66(6): 1342-55.
  • 5Menon S, Rosenberg K, Graham SA, et al. Binding-site geometry and flexibility in DC-SIGN demonstrated with surface force measurements. Proc Natl Acad Sci USA, 2009, 106(28): 11524-9.
  • 6Ellies LG, Tsuboi S, Petryniak B, et al. Core 2 oligosacc- haride biosynthesis distinguishes between selectin ligands essential for leukocyte homing and inflammation. Immunity, 1998, 9(6): 881-90.
  • 7Homeister JW, Thall AD, Petryniak B, et al. The ct(1,3) fucosyltransferases FucT-IV and FucT-VII exert coll- aborative control over selectin-dependent leukocyte recruitment and lymphocyte homing. Immunity, 200 I, 15(i): 115-26.
  • 8Yeh JC, Hiraoka N, Petryniak B, et al. Novel sulfated lymphocyte homing receptors and their control by a Core 1 extension 131,3-Nacetylglucosaminyltransferase. Cell, 2001, 105(7): 957-69.
  • 9McEver RP, Moore KL, Cummings RD. Leukocyte trafficking mediated by selectin-carbohydrate interactions. J Biol Chem, 1995, 270(19): 11025-8.
  • 10Wilkins PP, McEver RP, Cummings RD. Structures of the O-glycans on Pselectin glycoprotein ligand-1 from HL-60 cells. J Biol Chem, 1996, 271(31): 18732-42.

同被引文献21

  • 1高冬玲,陈奎生,赵志华,张红新,张岚,张云汉.食管鳞状细胞癌组织中MTA1和E-cadherin蛋白的表达[J].郑州大学学报(医学版),2007,42(6):1028-1030. 被引量:5
  • 2inoue M, Ton SM, Ogawa H, et al. Expression of Tn and sialyl-Tn antigens in tumor tissues of the ovary. Am J Clin Pathol,1991,96(6) : 711-716.
  • 3Ju T, Cummings RD. Protein glycosylation: chaperone mutation in Tnsyndrome [ J ]. Nature, 2005,437 ( 7063 ) : 1252 -1263.
  • 4Crew VK,Singleton BK,Green C ,et al. New mutations in C1GALT1 C1 in individuals with Tn Positive Phenotype [ J ]. Br J Haematol, 2008, 142(4) :657-667.
  • 5Ju T,Aryal RP,Stowell CJ,et al. Regulation of protein O-glycosylation by the endoplasmie reticulum-localized molceular chaperone Cosmc [ J]. J Cell Bioi,2008,182 (3):531-542.
  • 6Li C,Z Chen,Z Liu,et aL Correlation of expression and methylati0n of imprinted genes with pluripotency of parthenogenetic embryonic stem cells[J]. Hum Mol Genet,2009, 18(5) :2177-2187.
  • 7Gong SP,H Kim, F-3 Lee, et al. Change in gene expression of mouse embryonic stem cells derived from parthenogenetic activation[ J ]. Hum Reprod,2009,24 ( 7 ) : 805-814.
  • 8Koji T,Hiroyuki F, Masaharu K,et al. Expression of Tn and Sialyl-Tn Antigens in the Neoplastia Transformation otUterine Cervical Epithelial Cells[J]. Cancer Res,1996,56:2229-2232.
  • 9Parimal RDr Immunoreaetive T and Tn Antigens in Malignancy:Role in Carcinoma Diagnosis, Prognosis, and immunotherapy[ J ]. TransfusionMedicine Reviews,2000,14(4) : 312-325.
  • 10Semczuk A, Paszkowska A, Miturski R, et al. Sialosyl-Tn expression in normal and pathological conditions of human endometrium. At/ immunohistoehemical study [ J ]. Pathol Res Pratt, 2002, 19g ( 9 ) : 589-595.

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