Kumar R, Potvin B, Muller W A, Stanley P
Department of Cell Biology, Albert Einstein College of Medicine, New York 10461.
J Biol Chem. 1991 Nov 15;266(32):21777-83.
In previous studies, Chinese hamster ovary (CHO) cell genomic DNA transfectants that expressed a human alpha(1,3)-fucosyltransferase (alpha(1,3)Fuc-T) gene were isolated and shown to possess a common approximately 7.5-kilobase (kb) EcoRI fragment that hybridized to an Alu probe (Potvin, B., Kumar, R., Howard, D. R., and Stanley, P. (1990) J. Biol. Chem. 265, 1615-1622). One of these transfectants was used to make a genomic DNA library in lambda ZAP-II from EcoRI-digested, size-selected (6-8 kb) DNA, and plaques that hybridized to an Alu probe were purified. After in vivo excision, two plasmids with DNA inserts greater than or equal to 6 kb were obtained and one of these (D2.1) conferred human alpha(1,3)-Fuc-T activity on CHO transfectants. A partial restriction map of this clone revealed an approximately 3.6-kb PstI fragment that contained an Alu sequence. This fragment was subcloned into pGEM-3Zf(+) and compared by restriction analyses with a previously described approximately 3.6-kb PstI DNA fragment isolated from a human peripheral blood lymphocyte library and shown to encode an alpha(1,3)-Fuc-T gene (Lowe, J. B., Stoolman, L. M., Nair, R. P., Larsen, R. D., Berhend, T. L., and Marks, R. M. (1990) Cell 63, 475-484). Both approximately 3.6-kb fragments gave identical restriction patterns. In addition, they both caused CHO transfectants to synthesize the Lex determinant Gal beta(1,4)[Fuc alpha(1,3)]GlcNAc beta 1 but not the alpha(2,3)-sialyl-Lex determinant. As expected, these transfectants did not bind to ELAM-1 on activated endothelial cells, since sialyl-Lex is a carbohydrate ligand recognized by ELAM-1. Surprisingly, however, an open reading frame encoded within the approximately 3.6-kb PstI fragment had a sequence identical to that of ELFT, an alpha(1,3)-Fuc-T previously reported to confer ELAM-1 binding on a previously reported to confer ELAM-1 binding on a CHO transfectant (Goelz, S. E., Hession, C., Goff, D., Griffiths, B., Tizard, R., Newman, B., Chi-Rosso, G., and Lobb, R., (1990) Cell 63, 1349-1356). Possible explanations for these apparently disparate results are discussed.
在先前的研究中,分离出了表达人α(1,3)-岩藻糖基转移酶(α(1,3)Fuc-T)基因的中国仓鼠卵巢(CHO)细胞基因组DNA转染子,并显示其具有一个与Alu探针杂交的约7.5千碱基(kb)的常见EcoRI片段(Potvin,B.,Kumar,R.,Howard,D. R.,和Stanley,P.(1990)《生物化学杂志》265,1615 - 1622)。其中一个转染子用于从经EcoRI消化、大小选择(6 - 8 kb)的DNA构建λZAP-II基因组DNA文库,纯化与Alu探针杂交的噬菌斑。体内切除后,获得了两个DNA插入片段大于或等于6 kb的质粒,其中一个(D2.1)赋予CHO转染子人α(1,3)-Fuc-T活性。该克隆的部分限制性图谱显示一个约3.6 kb的PstI片段,其中包含一个Alu序列。将该片段亚克隆到pGEM-3Zf(+)中,并通过限制性分析与先前从人外周血淋巴细胞文库中分离出的、显示编码α(1,3)-Fuc-T基因的约3.6 kb PstI DNA片段进行比较(Lowe,J. B.,Stoolman,L. M.,Nair,R. P.,Larsen,R. D.,Berhend,T. L.,和Marks,R. M.(1990)《细胞》63,475 - 484)。两个约3.6 kb的片段给出了相同的限制性图谱。此外,它们都使CHO转染子合成Lex决定簇Galβ(1,4)[Fucα(1,3)]GlcNAcβ1,但不合成α(2,3)-唾液酸化-Lex决定簇。正如预期的那样,这些转染子不与活化内皮细胞上的ELAM-1结合,因为唾液酸化-Lex是ELAM-1识别的碳水化合物配体。然而,令人惊讶的是,在约3.6 kb的PstI片段内编码的一个开放阅读框的序列与ELFT相同,ELFT是先前报道的一种α(1,3)-Fuc-T,据报道它能使一个CHO转染子具有ELAM-1结合能力(Goelz,S. E.;Hession,C.;Goff,D.;Griffiths,B.;Tizard,R.;Newman,B.;Chi-Rosso,G.;和Lobb,R.(1990)《细胞》63,1349 - 1356)。讨论了这些明显不同结果的可能解释。