Identification and cloning of rat galectin-2: Expression is predominantly in epithelial cells of the stomach

Citation
T. Oka et al., Identification and cloning of rat galectin-2: Expression is predominantly in epithelial cells of the stomach, ARCH BIOCH, 361(2), 1999, pp. 195-201
Citations number
25
Categorie Soggetti
Biochemistry & Biophysics
Journal title
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS
ISSN journal
00039861 → ACNP
Volume
361
Issue
2
Year of publication
1999
Pages
195 - 201
Database
ISI
SICI code
0003-9861(19990115)361:2<195:IACORG>2.0.ZU;2-Y
Abstract
A complementary DNA clone preferentially expressed in the gastrointestinal tract was obtained from a rat stomach library. The protein coded by the clo ne had a single carbohydrate recognition domain having conserved motifs for beta-galactoside binding and showed 67% amino acid identity with human gal ectin-2. The recombinant protein synthesized in Escherich ia coli could bin d to an asialofetuin column and was eluted with beta-galactopyranoside. Fro m these observations, we named the protein rat galectin-2 coded by the cDNA . The rat galectin-2 was predominantly expressed in the epithelial cells of stomach. Thus this protein may form a mucin layer cross-linking with the b eta-galactoside moiety of glycoproteins. (C) 1999 Academic Press.