Heinonen Taisto Y K, Pelto-Huikko Markku, Pasternack Leena, Mäki Markku, Kainulainen Heikki
Paediatric Research Centre, University of Tampere Medical School and Tampere University Hospital, Tampere, Finland.
DNA Cell Biol. 2006 Aug;25(8):465-74. doi: 10.1089/dna.2006.25.465.
Glycosylation of proteins and lipids is important in cellular communication and maintenance of tissues. B3GTL (beta3-glycosyltransferase-like) is a novel glycosyltransferase that is found in multicellular animals ranging from mammals to insects and nematodes. The aim of this work was to identify and characterize the B3GTL gene in the mouse and to study its expression in various tissues. The murine gene codes for a protein which shares 84% amino acid sequence identity with its human ortholog, and contains all the primary structural features that characterize B3GTL proteins. The murine and human B3GTL genes share an identical exon/intron organization, and both genes utilize multiple polyadenylation signals. Their promoter regions show extensive conservation, implying that the two genes also share regulatory similarities. This notion was reinforced by Northern hybridization analysis of mouse tissues, which showed the tissue distribution of B3GTL mRNA to be similar to that previously found in human tissues, with the heart, kidney, and brain being major sites of expression in both species. The localization of B3GTL mRNA was studied by in situ hybridization in an extensive collection of mouse tissues, of which the granular cells of the olfactory bulb and the epithelium of the seminal vesicle displayed particularly strong signals. Together, these analyses indicate that the B3GTL mRNA is subject to strong tissue-specific and developmental regulation. The findings reported here make possible the design of a B3GTL "knock-out" mouse, provide a framework for analyzing the regulation of the gene, and provide an extensive catalog of tissues in which this novel protein acts.
蛋白质和脂质的糖基化在细胞通讯和组织维持中起着重要作用。B3GTL(β3-糖基转移酶样蛋白)是一种新型糖基转移酶,存在于从哺乳动物到昆虫和线虫的多细胞动物中。这项工作的目的是鉴定和表征小鼠中的B3GTL基因,并研究其在各种组织中的表达。小鼠基因编码的蛋白质与其人类直系同源物的氨基酸序列同一性为84%,并包含所有表征B3GTL蛋白质的主要结构特征。小鼠和人类的B3GTL基因具有相同的外显子/内含子组织,并且两个基因都利用多个聚腺苷酸化信号。它们的启动子区域显示出广泛的保守性,这意味着这两个基因也具有调控相似性。小鼠组织的Northern杂交分析强化了这一观点,该分析表明B3GTL mRNA的组织分布与先前在人类组织中发现的相似,心脏、肾脏和大脑是这两个物种中主要的表达部位。通过对大量小鼠组织进行原位杂交研究了B3GTL mRNA的定位,其中嗅球的颗粒细胞和精囊上皮显示出特别强的信号。总之,这些分析表明B3GTL mRNA受到强烈的组织特异性和发育调控。本文报道的研究结果使得设计B3GTL“敲除”小鼠成为可能,为分析该基因的调控提供了框架,并提供了该新型蛋白质发挥作用的广泛组织目录。