Tian E, Ten Hagen Kelly G
Developmental Glycobiology Unit, NIDCR, National Institutes of Health, Building 30, Room 426, 30 Convent Drive, MSC 4370, Bethesda, MD 20892-4370, USA.
Glycobiology. 2007 Aug;17(8):820-7. doi: 10.1093/glycob/cwm056. Epub 2007 May 23.
Mucin-type O-linked glycosylation is an evolutionarily conserved protein modification that is essential for viability in Drosophila melanogaster. However, the exact role of O-glycans and the identity of the crucial apoproteins modified with O-linked N-acetylgalactosamine (O-GalNAc) remain unknown. In an effort to elucidate the O-linked glycans expressed during Drosophila development, we have employed fluorescent confocal microscopy using a battery of lectins and an antibody specific for the GalNAcalpha-Ser/Thr structure (Tn antigen). Confocal microscopy provides high-resolution images of the diversity of glycans expressed in many developing organ systems. In particular, O-glycans are highly expressed on a number of ectodermally derived tissues such as the salivary glands, developing gut, and the tracheal system, suggesting a role for O-glycans in cell polarity and tube formation common to these organs. Additionally, O-glycans are found in the developing nervous system and within subregions of developing tissues known to be active in cell signaling events. This study provides us with temporal and spatial information regarding O-glycan expression as well as a set of reagents for the isolation of glycoproteins from specific developmental stages and organ systems. This information will aid us in identifying the in vivo substrates of the UDP-GalNAc: polypeptide N-acetylgalactosaminyltranferases, in a continuing effort to define the biological role of O-linked glycoproteins during development.
粘蛋白型O-连接糖基化是一种进化上保守的蛋白质修饰,对于黑腹果蝇的生存至关重要。然而,O-聚糖的确切作用以及被O-连接的N-乙酰半乳糖胺(O-GalNAc)修饰的关键载脂蛋白的身份仍然未知。为了阐明果蝇发育过程中表达的O-连接聚糖,我们使用了一系列凝集素和一种针对GalNAcα-Ser/Thr结构(Tn抗原)的抗体,采用荧光共聚焦显微镜技术。共聚焦显微镜提供了许多发育中的器官系统中表达的聚糖多样性的高分辨率图像。特别是,O-聚糖在许多外胚层衍生组织中高度表达,如唾液腺、发育中的肠道和气管系统,这表明O-聚糖在这些器官共有的细胞极性和管形成中发挥作用。此外,在发育中的神经系统以及已知在细胞信号事件中活跃的发育组织的亚区域中发现了O-聚糖。这项研究为我们提供了关于O-聚糖表达的时空信息,以及一组用于从特定发育阶段和器官系统中分离糖蛋白的试剂。这些信息将帮助我们识别UDP-GalNAc:多肽N-乙酰半乳糖胺基转移酶的体内底物,以持续努力确定O-连接糖蛋白在发育过程中的生物学作用。