Cloning, expression, and characterization of a novel UDP-galactose:beta-N-acetylglucosamine beta1,3-galactosyltransferase (beta3Gal-T5) responsible for synthesis of type 1 chain in colorectal and pancreatic epithelia and tumor cells derived therefrom

J Biol Chem. 1999 Apr 30;274(18):12499-507. doi: 10.1074/jbc.274.18.12499.

Abstract

The sialyl Lewis a antigen is a well known tumor marker, CA19-9, which is frequently elevated in the serum in gastrointestinal and pancreatic cancers. UDP-galactose:N-acetylglucosamine beta1, 3-galactosyltransferase(s) (beta3Gal-Ts) are required for the synthesis of the sialyl Lewis a epitope. In the present study, a novel beta3Gal-T, named beta3Gal-T5, was isolated from a Colo205 cDNA library using a degenerate primer strategy based on the amino acid sequences of the four human beta3Gal-T genes cloned to date. Transfection experiments demonstrated that HCT-15 cells transfected with the beta3Gal-T5 gene expressed all the type 1 Lewis antigens. In gastrointestinal and pancreatic cancer cell lines, the amounts of beta3Gal-T5 transcripts were quite well correlated with the amounts of the sialyl Lewis a antigens. The beta1,3Gal-T activity toward agalacto-lacto-N-neotetraose was also well correlated with the amounts of beta3Gal-T5 transcripts in a series of cultured cancer cells, and in Namalwa and HCT-15 cells transfected with the beta3Gal-T5 gene. Thus, the beta3Gal-T5 gene is the most probable candidate responsible for the synthesis of the type 1 Lewis antigens in gastrointestinal and pancreatic epithelia and tumor cells derived therefrom. In addition, beta3Gal-T5 is a key enzyme that determines the amounts of the type 1 Lewis antigens including the sialyl Lewis a antigen.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • CA-19-9 Antigen
  • Cloning, Molecular
  • Colorectal Neoplasms / enzymology*
  • Colorectal Neoplasms / immunology
  • Colorectal Neoplasms / pathology
  • DNA, Complementary
  • Gangliosides / immunology
  • Humans
  • Molecular Sequence Data
  • Pancreatic Neoplasms / enzymology*
  • Pancreatic Neoplasms / immunology
  • Pancreatic Neoplasms / pathology
  • RNA, Messenger / genetics
  • Sequence Homology, Amino Acid
  • Transferases (Other Substituted Phosphate Groups) / genetics*
  • Transferases (Other Substituted Phosphate Groups) / metabolism
  • Tumor Cells, Cultured

Substances

  • CA-19-9 Antigen
  • DNA, Complementary
  • Gangliosides
  • RNA, Messenger
  • sialyl Le(a) ganglioside
  • Transferases (Other Substituted Phosphate Groups)
  • UDPgalactose - UDP-N-acetylglucosamine galactosephosphotransferase

Associated data

  • GENBANK/AB020337