MOLECULAR-CLONING, EXPRESSION, CHROMOSOMAL ASSIGNMENT, AND TISSUE-SPECIFIC EXPRESSION OF A MURINE ALPHA-(1,3)-FUCOSYL-TRANSFERASE LOCUS CORRESPONDING TO THE HUMAN ELAM-1 LIGAND FUCOSYL-TRANSFERASE
Km. Gersten et al., MOLECULAR-CLONING, EXPRESSION, CHROMOSOMAL ASSIGNMENT, AND TISSUE-SPECIFIC EXPRESSION OF A MURINE ALPHA-(1,3)-FUCOSYL-TRANSFERASE LOCUS CORRESPONDING TO THE HUMAN ELAM-1 LIGAND FUCOSYL-TRANSFERASE, The Journal of biological chemistry, 270(42), 1995, pp. 25047-25056
Terminal Fuc alpha 1-3GlcNAc moieties are displayed by mammalian cell
surface glycoconjugates in a tissue-specific manner. These oligosaccha
rides participate in selectin-dependent leukocyte adhesion and have be
en implicated in adhesive events during murine embryogenesis. Other fu
nctions for these molecules remain to be defined, as do the tissue-spe
cific expression patterns of the corresponding alpha-(1-3)-fucosyltran
sferase (alpha 1-3FT) genes. This report characterizes a murine alpha
1-3FT that shares 77% amino acid sequence identity with human ELAM lig
and fucosyltransferase (ELFT, also termed Fuc-TIV). The corresponding
gene maps to mouse chromosome 9 in a region of homology with the Fuc-T
IV locus on human chromosome 11q. In vitro, the murine (alpha 1-3FT ca
n efficiently fucosylate the trisaccharide Gal alpha 1-3Gal beta 1-4Gl
cNAc (apparent K-m of 0.71 mM) to form an unusual tetrasaccharide (Gal
alpha 1-3Gal beta 1-4[Fuc alpha 1-3]GlcNAc) described in periimplanta
tion mouse tissues. The enzyme can also form the Lewis x determinant f
rom Gal beta 1-4GlcNAc (K-m = 2.05 mM), and the sialyl Lewis x determi
nant from NeuNAc alpha 2-3Gal beta 1-4GlcNAc (K-m = 1.78 mM). However,
it does not yield sialyl Lewis x determinants when expressed in a mam
malian cell line that maintains sialyl Lewis x precursors. Transcripts
from this gene accumulate to low levels in hematopoietic organs, but
are unexpectedly abundant in epithelia that line the stomach, small in
testine, colon, and epididymus. Epithelial cell-specific expression of
this gene suggests function(s) in addition to, and distinct from, its
proposed role in selectin ligand synthesis.