Oulmouden A, Wierinckx A, Petit J M, Costache M, Palcic M M, Mollicone R, Oriol R, Julien R
Institut de Biotechnologie, Faculté des Sciences, Université de Limoges, 87060 Limoges, France.
J Biol Chem. 1997 Mar 28;272(13):8764-73. doi: 10.1074/jbc.272.13.8764.
Only one bovine gene, corresponding to the human cluster of genes FUT3-FUT5-FUT6, was found by Southern blot analysis. The cognate bovine alpha(1,3)-fucosyltransferase shares 67.3, 69.0, and 69.3% amino acid sequence identities with human FUC-T3, FUC-T5, and FUC-T6 enzymes, respectively. As revealed by protein sequence alignment, potential sites for asparagine-linked glycosylation and conserved cysteines, the bovine enzyme is an intermediate between FUC-T3, FUC-T5, and FUC-T6 human enzymes. Transfected into COS-7 cells, the bovine gene induced the synthesis of an alpha(1, 3)-fucosyltransferase enzyme with type 2 substrate acceptor pattern specificity and induced expression of fucosylated type 2 epitopes (Lex and sialyl-Lex), but not of type 1 structures (Lea or sialyl-Lea), suggesting that it has an acceptor specificity similar to the human plasma FUC-T6. However, no enzyme activity was detected in bovine plasma. Gene transcripts are detected on tissues such as bovine liver, kidney, lung, and brain. The type 2 sialyl-Lex epitope was found in renal macula densa and biliary ducts, and Lex and Ley epitopes were detected on the brush border of epithelial cells of small and large intestine, suggesting a tissue distribution closer to human FUC-T3, but fucosylated type 1 structures (Lea, Leb, or sialyl-Lea) were not detected at all in any bovine tissue. Analysis of genetic distances on a combined phylogenetic tree of fucosyltransferase genes suggests that the bovine gene is the orthologous homologue of the ancestor of human genes constituting the present FUT3-FUT5-FUT6 cluster.
通过Southern印迹分析仅发现了一个与人类FUT3 - FUT5 - FUT6基因簇相对应的牛基因。同源的牛α(1,3)-岩藻糖基转移酶与人类FUC - T3、FUC - T5和FUC - T6酶的氨基酸序列同一性分别为67.3%、69.0%和69.3%。蛋白质序列比对显示,该牛酶具有天冬酰胺连接糖基化的潜在位点和保守的半胱氨酸,它是人类FUC - T3、FUC - T5和FUC - T6酶之间的中间类型。将该牛基因转染到COS - 7细胞中,可诱导合成具有2型底物受体模式特异性的α(1,3)-岩藻糖基转移酶,并诱导岩藻糖基化2型表位(Lex和唾液酸化Lex)的表达,但不诱导1型结构(Lea或唾液酸化Lea)的表达,这表明它具有与人类血浆FUC - T6相似的受体特异性。然而,在牛血浆中未检测到酶活性。在牛的肝脏、肾脏、肺和脑等组织中检测到了基因转录本。在肾致密斑和胆管中发现了2型唾液酸化Lex表位,在小肠和大肠上皮细胞的刷状缘检测到了Lex和Ley表位,这表明其组织分布更接近人类FUC - T3,但在任何牛组织中均未检测到岩藻糖基化的1型结构(Lea、Leb或唾液酸化Lea)。对岩藻糖基转移酶基因联合系统发育树的遗传距离分析表明,该牛基因是构成当前FUT3 - FUT5 - FUT6基因簇的人类基因祖先的直系同源物。