Cloning of a human alpha(1,3)-fucosyltransferase gene that encodes ELFT but does not confer ELAM-1 recognition on Chinese hamster ovary cell transfectants

J Biol Chem. 1991 Nov 15;266(32):21777-83.

Abstract

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.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Antibodies, Monoclonal
  • Antigen-Antibody Complex
  • Base Sequence
  • CHO Cells
  • Cell Adhesion
  • Cell Adhesion Molecules / metabolism*
  • Cloning, Molecular / methods
  • Cricetinae
  • E-Selectin
  • Endothelium, Vascular / metabolism*
  • Escherichia coli / genetics
  • Fucosyltransferases / genetics*
  • Fucosyltransferases / metabolism
  • Genetic Vectors
  • Genomic Library
  • Humans
  • Lewis X Antigen / analysis
  • Molecular Sequence Data
  • Plasmids
  • Restriction Mapping
  • Transfection*

Substances

  • Antibodies, Monoclonal
  • Antigen-Antibody Complex
  • Cell Adhesion Molecules
  • E-Selectin
  • Lewis X Antigen
  • Fucosyltransferases
  • galactoside 3-fucosyltransferase

Associated data

  • GENBANK/M57984
  • GENBANK/M57985
  • GENBANK/M57986
  • GENBANK/M57987
  • GENBANK/S65147
  • GENBANK/S65149
  • GENBANK/S65151
  • GENBANK/S65153
  • GENBANK/S65155
  • GENBANK/S65161