Narimatsu Hisashi
Glycogene Function Team, Research Center for Glycoscience, National Institute of Advanced Industrial Science and Technology (AIST), OSL C-2, 1-1-1 Umezono, Tsukuba, Ibaraki, 305-8568, Japan.
Glycoconj J. 2004;21(1-2):17-24. doi: 10.1023/B:GLYC.0000043742.99482.01.
Eighteen years have passed after the first mammalian glycosyltransferase was cloned. At the beginning of April, 2001, 110 genes for human glycosyltransferases, including modifying enzymes for carbohydrate chains such as sulfotransferases, had been cloned and analyzed. We started the Glycogene Project (GG project) in April 2001, a comprehensive study on human glycogenes with the aid of bioinformatic technology. The term glycogene includes the genes for glycosyltransferases, sulfotransferases adding sulfate to carbohydrates and sugar-nucleotide transporters, etc. Firstly, as many novel genes, which are the candidates for glycogenes, as possible were searched using bioinformatic technology in databases. They were then cloned and expressed in various expression systems to detect the activity for carbohydrate synthesis. Their substrate specificity was determined using various acceptors.
自首个哺乳动物糖基转移酶被克隆以来,已经过去了18年。2001年4月初,包括硫酸转移酶等碳水化合物链修饰酶在内的110个人类糖基转移酶基因已被克隆和分析。我们于2001年4月启动了糖基因项目(GG项目),借助生物信息学技术对人类糖基因进行全面研究。糖基因一词包括糖基转移酶基因、向碳水化合物添加硫酸盐的硫酸转移酶基因以及糖核苷酸转运体基因等。首先,利用生物信息学技术在数据库中搜索尽可能多的作为糖基因候选的新基因。然后将它们克隆并在各种表达系统中表达,以检测碳水化合物合成活性。使用各种受体确定它们的底物特异性。