Glycobiology, 2000, Vol. 10, No. 8 789-802
© 2000 Oxford University Press
FUT4 and FUT9 genes are expressed early in human embryogenesis
U 504 INSERM, Université de Paris Sud XI, 94807 Villejuif, France, 2UMR 1599 CNRS, Cytogénétique, IGR, 94805 Villejuif, France, and 3Hôpital de Pontoise, 95300 Pontoise, France
The Lex oligosaccharide is expressed in organ buds progressing in mesenchyma, during human embryogenesis. Myeloid-like
3-fucosyltransferases are good candidates to synthesize this oligosaccharide. We investigated by Northern analysis all the
3-fucosyltransferase gene transcripts and only FUT4 and FUT9 were detected. The enzymes encoded by the FUT4 and FUT9 genes are the first
3-fucosyltransferases strongly expressed during the first two months of embryogenesis. The Northern profile of expression of the embryo FUT4 transcripts is similar in size and sequence to the known FUT4 transcripts of 6 kb, 3 kb, and 2.3 kb, but a new FUT9 transcript of 2501 bp, different from the known mouse (2170 bp) and human (3019 bp) transcripts was cloned. FUT3, FUT5, FUT6, and FUT7 were not detected by Northern blot. The FUT3 and FUT6 transcripts start to appear at this stage, but are only detected by reverse transcriptase-PCR analysis. The expression of FUT5 is weaker than FUT3 and FUT6 and the RT-PCR signal is faint and irregular. FUT7 is not detected at all. Using mRNA from 40- to 65-day-old embryos, we have prepared different hexamer and oligo-dT cDNA libraries and cloned, by rapid amplification cDNA ends-PCR, FUT4 and FUT9
3-fucosyltransferase transcripts. The tissue expression of the embryonic FUT9 transcript is closer to that observed for the mouse (brain), than to the known human (stomach) transcripts. The acceptor specificity and the kinetics of the
3-fucosyltransferase encoded by this FUT9 transcript are similar to the FUT4 enzyme, except for the utilization of the lac-di-NAc acceptor which is not efficiently transformed by the FUT9 enzyme. Like FUT4, this embryonic FUT9 is N-ethylmaleimide and heat resistant and the corresponding gene was confirmed to be localized in the chromosome band 6q16. Finally, this FUT9 transcript has a single expressed exon as has been observed for most of the other vertebrate
2- and
3-fucosyltransferases.
1 To whom correspondence should be addressed at: U 504 INSERM, 16 Av. Paul Vaillant-Couturier, 94807 Villejuif CEDEX, France
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
M. Sikora, A. Ferrer-Admetlla, H. Laayouni, C. Menendez, A. Mayor, A. Bardaji, B. Sigauque, I. Mandomando, P. L. Alonso, J. Bertranpetit, et al. A variant in the gene FUT9 is associated with susceptibility to placental malaria infection Hum. Mol. Genet., August 15, 2009; 18(16): 3136 - 3144. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Mollicone, S. E. H. Moore, N. Bovin, M. Garcia-Rosasco, J.-J. Candelier, I. Martinez-Duncker, and R. Oriol Activity, Splice Variants, Conserved Peptide Motifs, and Phylogeny of Two New {alpha}1,3-Fucosyltransferase Families (FUT10 and FUT11) J. Biol. Chem., February 13, 2009; 284(7): 4723 - 4738. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Allahverdian, K. R. Wojcik, and D. R. Dorscheid Airway epithelial wound repair: role of carbohydrate sialyl Lewisx Am J Physiol Lung Cell Mol Physiol, October 1, 2006; 291(4): L828 - L836. [Abstract] [Full Text] [PDF] |
||||
![]() |
Z. S. Kawar, S. M. Haslam, H. R. Morris, A. Dell, and R. D. Cummings Novel Poly-GalNAc{beta}1-4GlcNAc (LacdiNAc) and Fucosylated Poly-LacdiNAc N-Glycans from Mammalian Cells Expressing {beta}1,4-N-Acetylgalactosaminyltransferase and {alpha}1,3-Fucosyltransferase J. Biol. Chem., April 1, 2005; 280(13): 12810 - 12819. [Abstract] [Full Text] [PDF] |
||||
![]() |
I. Martinez-Duncker, T. Dupre, V. Piller, F. Piller, J.-J. Candelier, C. Trichet, G. Tchernia, R. Oriol, and R. Mollicone Genetic complementation reveals a novel human congenital disorder of glycosylation of type II, due to inactivation of the Golgi CMP-sialic acid transporter Blood, April 1, 2005; 105(7): 2671 - 2676. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. Kudo, M. Kaneko, H. Iwasaki, A. Togayachi, S. Nishihara, K. Abe, and H. Narimatsu Normal Embryonic and Germ Cell Development in Mice Lacking {alpha}1,3-Fucosyltransferase IX (Fut9) Which Show Disappearance of Stage-Specific Embryonic Antigen 1 Mol. Cell. Biol., May 15, 2004; 24(10): 4221 - 4228. [Abstract] [Full Text] [PDF] |
||||
![]() |
I. Martinez-Duncker, J.-C. Michalski, C. Bauvy, J.-J. Candelier, B. Mennesson, P. Codogno, R. Oriol, and R. Mollicone Activity and tissue distribution of splice variants of {alpha}6-fucosyltransferase in human embryogenesis Glycobiology, January 1, 2004; 14(1): 13 - 25. [Abstract] [Full Text] [PDF] |
||||
![]() |
I. Martinez-Duncker, R. Mollicone, J.-J. Candelier, C. Breton, and R. Oriol A new superfamily of protein-O-fucosyltransferases, {alpha}2-fucosyltransferases, and {alpha}6-fucosyltransferases: phylogeny and identification of conserved peptide motifs Glycobiology, December 1, 2003; 13(12): 1C - 5C. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Oriol, I. Martinez-Duncker, I. Chantret, R. Mollicone, and P. Codogno Common Origin and Evolution of Glycosyltransferases Using Dol-P-monosaccharides as Donor Substrate Mol. Biol. Evol., September 1, 2002; 19(9): 1451 - 1463. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Toivonen, S. Nishihara, H. Narimatsu, O. Renkonen, and R. Renkonen Fuc-TIX: a versatile {alpha}1,3-fucosyltransferase with a distinct acceptor- and site-specificity profile Glycobiology, June 1, 2002; 12(6): 361 - 368. [Abstract] [Full Text] [PDF] |
||||
![]() |
T. de Vries, R. M.A. Knegtel, E. H. Holmes, and B. A. Macher Fucosyltransferases: structure/function studies Glycobiology, October 1, 2001; 11(10): 119R - 128R. [Abstract] [Full Text] [PDF] |
||||






