Sasaki K, Kurata K, Kojima N, Kurosawa N, Ohta S, Hanai N, Tsuji S, Nishi T
Tokyo Research Laboratories, Kyowa Hakko Kogyo, Co., Ltd., Japan.
J Biol Chem. 1994 Jun 3;269(22):15950-6.
A cDNA encoding a GM3-specific alpha-2,8-sialyltransferase (GD3 synthase) was obtained from an expression cDNA library of human melanoma cell line WM266-4 by enrichment of Namalwa KJM-1 cells highly expressing GD3 using an anti-GD3 antibody and a fluorescence-activated cell sorter. Selection of B-cell line Namalwa cells expressing transfected cDNAs in the presence of anti-GD3 monoclonal antibody KM641 gave a cDNA (pAMo-GD3) encoding a protein with a type II transmembrane topology as found for mammalian glycosyltransferases. The following evidence confirms that the cDNA encodes an alpha-2,8-sialyltransferase, which specifically converts GM3 to GD3. (i) Transfection of pAMo-GD3 into Namalwa KJM-1 cells leads to the appearance of GD3 and a GD3 synthase activity. (ii) Northern blot analysis revealed a correlation between the expression of this gene and GD3 in several cell lines. (iii) The putative COOH-terminal active domain of this cloned enzyme fused with protein A has been purified with IgG-Sepharose beads and has been shown to possess GD3-synthesizing activity, excluding the possibility that the cloned cDNA encodes a transacting factor inducing a GD3 synthase. The deduced primary sequence also contains the "sialyl motif" conserved among all the sialyltransferases cloned to date. The polymerase chain reaction analysis reveals that this gene is located on chromosome 12.
通过使用抗GD3抗体和荧光激活细胞分选仪富集高表达GD3的Namalwa KJM-1细胞,从人黑色素瘤细胞系WM266-4的表达cDNA文库中获得了编码GM3特异性α-2,8-唾液酸转移酶(GD3合酶)的cDNA。在抗GD3单克隆抗体KM641存在的情况下,选择表达转染cDNA的B细胞系Namalwa细胞,得到了一个编码具有II型跨膜拓扑结构蛋白质的cDNA(pAMo-GD3),这与哺乳动物糖基转移酶的情况相同。以下证据证实该cDNA编码一种α-2,8-唾液酸转移酶,它能将GM3特异性转化为GD3。(i)将pAMo-GD3转染到Namalwa KJM-1细胞中导致GD3出现和GD3合酶活性。(ii)Northern印迹分析揭示了该基因在几种细胞系中的表达与GD3之间的相关性。(iii)该克隆酶的推定COOH末端活性结构域与蛋白A融合后已用IgG-琼脂糖珠纯化,并已显示具有GD3合成活性,排除了克隆的cDNA编码诱导GD3合酶的反式作用因子的可能性。推导的一级序列还包含了迄今为止克隆的所有唾液酸转移酶中保守的“唾液酸基序”。聚合酶链反应分析表明该基因位于12号染色体上。