Skip to main content
Biochemical Journal logoLink to Biochemical Journal
. 2000 Nov 15;352(Pt 1):37–48.

Cloning, expression and gene organization of a human Neu5Ac alpha 2-3Gal beta 1-3GalNAc alpha 2,6-sialyltransferase: hST6GalNAcIV.

A Harduin-Lepers 1, D C Stokes 1, W F Steelant 1, B Samyn-Petit 1, M A Krzewinski-Recchi 1, V Vallejo-Ruiz 1, J P Zanetta 1, C Augé 1, P Delannoy 1
PMCID: PMC1221430  PMID: 11062056

Abstract

On the basis of the detection of expressed sequence tag ('EST') similar to the rat N-acetylgalactosamine alpha2,6-sialyltransferase (ST6GalNAc) III cDNA, we have identified a novel member of the human ST6GalNAc family. We have isolated a cDNA clone containing an open reading frame that codes for a type II membrane protein of 302 amino acids with a seven-amino-acid cytoplasmic domain, an 18-amino-acid transmembrane domain and the smallest described catalytic domain of 277 amino acids. This predicted sialyltransferase sequence is similar to the rat ST6GalNAc III (46.6%), but was found to be even more similar to the recently reported mouse ST6GalNAc IV (88.1%) on the basis of amino acid sequence identity. Northern-blot analysis showed that the newly identified gene is expressed constitutively in various adult human tissues as a 2.2kb transcript, but was also found to be expressed at lower levels in brain, heart and skeletal muscle as a 2.5kb transcript. Expression of the hST6GalNAc IV gene was investigated by reverse transcription PCR in various human cancer cells, and was found to be present in the majority of cell types with the exception of the carcinoma cell line T47D and pro-monocyte THP cells. The transient expression in COS-7 cells of the full-length cDNA led to the production of an active enzyme sharing the acceptor specificity of the ST6GalNAc family towards Neu5Ac alpha 2-3Gal beta 1-3GalNAc alpha-O-R (where 'R' denotes H, benzyl, or a peptidic chain). Detailed analysis in vitro of substrate specificity revealed that the enzyme required the trisaccharide Neu5Ac alpha 2-3Gal beta1-3GalNAc found on O-glycans and arylglycosides. In addition, we have clarified the genomic organization of ST6GalNAc IV gene.

Full Text

The Full Text of this article is available as a PDF (286.0 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Almeida R., Amado M., David L., Levery S. B., Holmes E. H., Merkx G., van Kessel A. G., Rygaard E., Hassan H., Bennett E. A family of human beta4-galactosyltransferases. Cloning and expression of two novel UDP-galactose:beta-n-acetylglucosamine beta1, 4-galactosyltransferases, beta4Gal-T2 and beta4Gal-T3. J Biol Chem. 1997 Dec 19;272(51):31979–31991. doi: 10.1074/jbc.272.51.31979. [DOI] [PubMed] [Google Scholar]
  2. Altschul S. F., Madden T. L., Schäffer A. A., Zhang J., Zhang Z., Miller W., Lipman D. J. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res. 1997 Sep 1;25(17):3389–3402. doi: 10.1093/nar/25.17.3389. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Amado M., Almeida R., Carneiro F., Levery S. B., Holmes E. H., Nomoto M., Hollingsworth M. A., Hassan H., Schwientek T., Nielsen P. A. A family of human beta3-galactosyltransferases. Characterization of four members of a UDP-galactose:beta-N-acetyl-glucosamine/beta-nacetyl-galactosamine beta-1,3-galactosyltransferase family. J Biol Chem. 1998 May 22;273(21):12770–12778. doi: 10.1074/jbc.273.21.12770. [DOI] [PubMed] [Google Scholar]
  4. Baubichon-Cortay H., Serres-Guillaumond M., Louisot P., Broquet P. A brain sialyltransferase having a narrow specificity for O-glycosyl-linked oligosaccharide chains. Carbohydr Res. 1986 Jun 1;149(1):209–223. doi: 10.1016/s0008-6215(00)90379-3. [DOI] [PubMed] [Google Scholar]
  5. Chang M. L., Eddy R. L., Shows T. B., Lau J. T. Three genes that encode human beta-galactoside alpha 2,3-sialyltransferases. Structural analysis and chromosomal mapping studies. Glycobiology. 1995 May;5(3):319–325. doi: 10.1093/glycob/5.3.319. [DOI] [PubMed] [Google Scholar]
  6. Datta A. K., Paulson J. C. Sialylmotifs of sialyltransferases. Indian J Biochem Biophys. 1997 Feb-Apr;34(1-2):157–165. [PubMed] [Google Scholar]
  7. Eckhardt M., Gerardy-Schahn R. Genomic organization of the murine polysialyltransferase gene ST8SiaIV (PST-1). Glycobiology. 1998 Dec;8(12):1165–1172. doi: 10.1093/glycob/8.12.1165. [DOI] [PubMed] [Google Scholar]
  8. Fukutomi T., Hirohashi S., Tsuda H., Nanasawa T., Yamamoto H., Itabashi M., Shimosato Y. The prognostic value of tumor-associated carbohydrate structures correlated with gene amplifications in human breast carcinomas. Jpn J Surg. 1991 Sep;21(5):499–507. doi: 10.1007/BF02470985. [DOI] [PubMed] [Google Scholar]
  9. Geremia R. A., Harduin-Lepers A., Delannoy P. Identification of two novel conserved amino acid residues in eukaryotic sialyltransferases: implications for their mechanism of action. Glycobiology. 1997 Mar;7(2):v–vii. doi: 10.1093/glycob/7.2.161. [DOI] [PubMed] [Google Scholar]
  10. Gilley J., Fried M. Extensive gene order differences within regions of conserved synteny between the Fugu and human genomes: implications for chromosomal evolution and the cloning of disease genes. Hum Mol Genet. 1999 Jul;8(7):1313–1320. doi: 10.1093/hmg/8.7.1313. [DOI] [PubMed] [Google Scholar]
  11. Hakomori S. Possible functions of tumor-associated carbohydrate antigens. Curr Opin Immunol. 1991 Oct;3(5):646–653. doi: 10.1016/0952-7915(91)90091-e. [DOI] [PubMed] [Google Scholar]
  12. Harduin-Lepers A., Recchi M. A., Delannoy P. 1994, the year of sialyltransferases. Glycobiology. 1995 Dec;5(8):741–758. doi: 10.1093/glycob/5.8.741. [DOI] [PubMed] [Google Scholar]
  13. Hennet T., Dinter A., Kuhnert P., Mattu T. S., Rudd P. M., Berger E. G. Genomic cloning and expression of three murine UDP-galactose: beta-N-acetylglucosamine beta1,3-galactosyltransferase genes. J Biol Chem. 1998 Jan 2;273(1):58–65. doi: 10.1074/jbc.273.1.58. [DOI] [PubMed] [Google Scholar]
  14. Ikehara Y., Kojima N., Kurosawa N., Kudo T., Kono M., Nishihara S., Issiki S., Morozumi K., Itzkowitz S., Tsuda T. Cloning and expression of a human gene encoding an N-acetylgalactosamine-alpha2,6-sialyltransferase (ST6GalNAc I): a candidate for synthesis of cancer-associated sialyl-Tn antigens. Glycobiology. 1999 Nov;9(11):1213–1224. doi: 10.1093/glycob/9.11.1213. [DOI] [PubMed] [Google Scholar]
  15. Ikehara Y., Shimizu N., Kono M., Nishihara S., Nakanishi H., Kitamura T., Narimatsu H., Tsuji S., Tatematsu M. A novel glycosyltransferase with a polyglutamine repeat; a new candidate for GD1alpha synthase (ST6GalNAc V)(1). FEBS Lett. 1999 Dec 10;463(1-2):92–96. doi: 10.1016/s0014-5793(99)01605-1. [DOI] [PubMed] [Google Scholar]
  16. Kelm S., Schauer R. Sialic acids in molecular and cellular interactions. Int Rev Cytol. 1997;175:137–240. doi: 10.1016/S0074-7696(08)62127-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Kitagawa H., Mattei M. G., Paulson J. C. Genomic organization and chromosomal mapping of the Gal beta 1,3GalNAc/Gal beta 1,4GlcNAc alpha 2,3-sialyltransferase. J Biol Chem. 1996 Jan 12;271(2):931–938. doi: 10.1074/jbc.271.2.931. [DOI] [PubMed] [Google Scholar]
  18. Kjeldsen T., Clausen H., Hirohashi S., Ogawa T., Iijima H., Hakomori S. Preparation and characterization of monoclonal antibodies directed to the tumor-associated O-linked sialosyl-2----6 alpha-N-acetylgalactosaminyl (sialosyl-Tn) epitope. Cancer Res. 1988 Apr 15;48(8):2214–2220. [PubMed] [Google Scholar]
  19. Kozak M. Regulation of translation in eukaryotic systems. Annu Rev Cell Biol. 1992;8:197–225. doi: 10.1146/annurev.cb.08.110192.001213. [DOI] [PubMed] [Google Scholar]
  20. Kurosawa N., Hamamoto T., Lee Y. C., Nakaoka T., Kojima N., Tsuji S. Molecular cloning and expression of GalNAc alpha 2,6-sialyltransferase. J Biol Chem. 1994 Jan 14;269(2):1402–1409. [PubMed] [Google Scholar]
  21. Kurosawa N., Inoue M., Yoshida Y., Tsuji S. Molecular cloning and genomic analysis of mouse Galbeta1, 3GalNAc-specific GalNAc alpha2,6-sialyltransferase. J Biol Chem. 1996 Jun 21;271(25):15109–15116. doi: 10.1074/jbc.271.25.15109. [DOI] [PubMed] [Google Scholar]
  22. Kurosawa N., Kojima N., Inoue M., Hamamoto T., Tsuji S. Cloning and expression of Gal beta 1,3GalNAc-specific GalNAc alpha 2,6-sialyltransferase. J Biol Chem. 1994 Jul 22;269(29):19048–19053. [PubMed] [Google Scholar]
  23. Kurosawa N., Takashima S., Kono M., Ikehara Y., Inoue M., Tachida Y., Narimatsu H., Tsuji S. Molecular cloning and genomic analysis of mouse GalNAc alpha2, 6-sialyltransferase (ST6GalNAc I). J Biochem. 2000 May;127(5):845–854. doi: 10.1093/oxfordjournals.jbchem.a022678. [DOI] [PubMed] [Google Scholar]
  24. Lee Y. C., Kaufmann M., Kitazume-Kawaguchi S., Kono M., Takashima S., Kurosawa N., Liu H., Pircher H., Tsuji S. Molecular cloning and functional expression of two members of mouse NeuAcalpha2,3Galbeta1,3GalNAc GalNAcalpha2,6-sialyltransferase family, ST6GalNAc III and IV. J Biol Chem. 1999 Apr 23;274(17):11958–11967. doi: 10.1074/jbc.274.17.11958. [DOI] [PubMed] [Google Scholar]
  25. Lo N. W., Shaper J. H., Pevsner J., Shaper N. L. The expanding beta 4-galactosyltransferase gene family: messages from the databanks. Glycobiology. 1998 May;8(5):517–526. doi: 10.1093/glycob/8.5.517. [DOI] [PubMed] [Google Scholar]
  26. Lubineau A., Augé C., François P. The use of porcine liver (2----3)-alpha-sialyltransferase in the large-scale synthesis of alpha-Neup5Ac-(2----3)-beta-D-Galp-(1----3)-D-GlcpNAc, the epitope of the tumor-associated carbohydrate antigen CA 50. Carbohydr Res. 1992 Apr 10;228(1):137–144. doi: 10.1016/s0008-6215(00)90555-x. [DOI] [PubMed] [Google Scholar]
  27. Lubineau A., Augé C., Gautheron-Le Narvor C., Ginet J. C. Combined chemical and enzymatic synthesis of the sialylated non reducing terminal sequence of GM1b glycolylated ganglioside, a potential human tumor marker. Bioorg Med Chem. 1994 Jul;2(7):669–674. doi: 10.1016/0968-0896(94)85016-x. [DOI] [PubMed] [Google Scholar]
  28. Lubineau A., Basset-Carpentier K., Augé C. Porcine liver (2-->3)-alpha-sialyltransferase: substrate specificity studies and application of the immobilized enzyme to the synthesis of various sialylated oligosaccharide sequences. Carbohydr Res. 1997 May 12;300(2):161–167. doi: 10.1016/s0008-6215(97)00043-8. [DOI] [PubMed] [Google Scholar]
  29. Nilsson B., Nordén N. E., Svensson S. Structural studies on the carbohydrate portion of fetuin. J Biol Chem. 1979 Jun 10;254(11):4545–4553. [PubMed] [Google Scholar]
  30. Okajima T., Fukumoto S., Ito H., Kiso M., Hirabayashi Y., Urano T., Furukawa K. Molecular cloning of brain-specific GD1alpha synthase (ST6GalNAc V) containing CAG/Glutamine repeats. J Biol Chem. 1999 Oct 22;274(43):30557–30562. doi: 10.1074/jbc.274.43.30557. [DOI] [PubMed] [Google Scholar]
  31. Samyn-Petit B., Krzewinski-Recchi M. A., Steelant W. F., Delannoy P., Harduin-Lepers A. Molecular cloning and functional expression of human ST6GalNAc II. Molecular expression in various human cultured cells. Biochim Biophys Acta. 2000 Apr 6;1474(2):201–211. doi: 10.1016/s0304-4165(00)00020-9. [DOI] [PubMed] [Google Scholar]
  32. Sanger F., Nicklen S., Coulson A. R. DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463–5467. doi: 10.1073/pnas.74.12.5463. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Schwientek T., Nomoto M., Levery S. B., Merkx G., van Kessel A. G., Bennett E. P., Hollingsworth M. A., Clausen H. Control of O-glycan branch formation. Molecular cloning of human cDNA encoding a novel beta1,6-N-acetylglucosaminyltransferase forming core 2 and core 4. J Biol Chem. 1999 Feb 19;274(8):4504–4512. doi: 10.1074/jbc.274.8.4504. [DOI] [PubMed] [Google Scholar]
  34. Sjoberg E. R., Kitagawa H., Glushka J., van Halbeek H., Paulson J. C. Molecular cloning of a developmentally regulated N-acetylgalactosamine alpha2,6-sialyltransferase specific for sialylated glycoconjugates. J Biol Chem. 1996 Mar 29;271(13):7450–7459. doi: 10.1074/jbc.271.13.7450. [DOI] [PubMed] [Google Scholar]
  35. Spiro R. G., Bhoyroo V. D. Structure of the O-glycosidically linked carbohydrate units of fetuin. J Biol Chem. 1974 Sep 25;249(18):5704–5717. [PubMed] [Google Scholar]
  36. Svensson E. C., Soreghan B., Paulson J. C. Organization of the beta-galactoside alpha 2,6-sialyltransferase gene. Evidence for the transcriptional regulation of terminal glycosylation. J Biol Chem. 1990 Dec 5;265(34):20863–20868. [PubMed] [Google Scholar]
  37. Takashima S., Yoshida Y., Kanematsu T., Kojima N., Tsuji S. Genomic structure and promoter activity of the mouse polysialic acid synthase (mST8Sia IV/PST) gene. J Biol Chem. 1998 Mar 27;273(13):7675–7683. doi: 10.1074/jbc.273.13.7675. [DOI] [PubMed] [Google Scholar]
  38. Tsuji S., Datta A. K., Paulson J. C. Systematic nomenclature for sialyltransferases. Glycobiology. 1996 Oct;6(7):v–vii. doi: 10.1093/glycob/6.7.647. [DOI] [PubMed] [Google Scholar]
  39. Tsuji T., Osawa T. Carbohydrate structures of bovine submaxillary mucin. Carbohydr Res. 1986 Aug 15;151:391–402. doi: 10.1016/s0008-6215(00)90358-6. [DOI] [PubMed] [Google Scholar]
  40. Varki A. Biological roles of oligosaccharides: all of the theories are correct. Glycobiology. 1993 Apr;3(2):97–130. doi: 10.1093/glycob/3.2.97. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Varki A. Selectin ligands. Proc Natl Acad Sci U S A. 1994 Aug 2;91(16):7390–7397. doi: 10.1073/pnas.91.16.7390. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Yoshida Y., Kurosawa N., Kanematsu T., Kojima N., Tsuji S. Genomic structure and promoter activity of the mouse polysialic acid synthase gene (mST8Sia II). Brain-specific expression from a TATA-less GC-rich sequence. J Biol Chem. 1996 Nov 22;271(47):30167–30173. doi: 10.1074/jbc.271.47.30167. [DOI] [PubMed] [Google Scholar]
  43. Yoshida Y., Kurosawa N., Kanematsu T., Taguchi A., Arita M., Kojima N., Tsuji S. Unique genomic structure and expression of the mouse alpha 2,8-sialyltransferase (ST8Sia III) gene. Glycobiology. 1996 Sep;6(6):573–580. doi: 10.1093/glycob/6.6.573. [DOI] [PubMed] [Google Scholar]
  44. Zanetta J. P., Gouyer V., Maes E., Pons A., Hemon B., Zweibaum A., Delannoy P., Huet G. Massive in vitro synthesis of tagged oligosaccharides in 1-benzyl-2-acetamido-2-deoxy-alpha-D-galactopyranoside treated HT-29 cells. Glycobiology. 2000 Jun;10(6):565–575. doi: 10.1093/glycob/10.6.565. [DOI] [PubMed] [Google Scholar]

Articles from Biochemical Journal are provided here courtesy of The Biochemical Society

RESOURCES