1999
DOI: 10.1016/s0014-5793(99)00640-7
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α1,3‐Fucoslytransferase IX (Fuc‐TIX) is very highly conserved between human and mouse; molecular cloning, characterization and tissue distribution of human Fuc‐TIX

Abstract: The amino acid sequence of Fuc-TIX is very highly conserved between mouse and human. The number of nonsynonymous nucleotide substitutions of the Fuc-TIX gene between human and mouse was strikingly low, and almost equivalent to that of the K K-actin gene. This indicates that Fuc-TIX is under a strong selective pressure of preservation during evolution. The human Fuc-TIX (hFuc-TIX) showed a unique characteristics, i.e. hFuc-TIX was not activated by Mn 2+ and Co 2+ , whereas hFuc-TIV and hFuc-TVI were activated b… Show more

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Cited by 116 publications
(84 citation statements)
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References 36 publications
(52 reference statements)
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“…Based on the sequences of mouse and human FucT-IX genes (44,49), oligonucleotides used to amplify the cDNA were as follows: 5Ј-ATGACATCAACATCCAAAGGCATT-3Ј and 5Ј-ACCAA-CAGACTTATATTCTTGATGCC-3Ј. The PCR product was subcloned into the pBluescript SKϪ, and the subcloned fragments were sequenced.…”
Section: Methodsmentioning
confidence: 99%
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“…Based on the sequences of mouse and human FucT-IX genes (44,49), oligonucleotides used to amplify the cDNA were as follows: 5Ј-ATGACATCAACATCCAAAGGCATT-3Ј and 5Ј-ACCAA-CAGACTTATATTCTTGATGCC-3Ј. The PCR product was subcloned into the pBluescript SKϪ, and the subcloned fragments were sequenced.…”
Section: Methodsmentioning
confidence: 99%
“…A series of mammalian ␣3FucT has been cloned to date. In human, six members of the ␣3FucT gene family, FucT-III (35), -IV (36 -38), -V (39), -VI (40,41), -VII (42,43), and -IX (44), have been identified and a subfamily, consisting of FucT-III, -V, and -VI, forms a gene cluster (45). In mouse, a homologue of FucT-III/V/VI has been reported to be a pseudogene (46), while FucT-IV, FucT-VII, and FucT-IX homologues are functional genes (46 -49).…”
mentioning
confidence: 99%
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“…FUT7 can only synthesize sLe x (9). FUT9 synthesizes Le x (10). FUT10 and FUT11 have been identified from the human genome since they have a conserved ·3 FT domain (11), however their activity has not been validated (12).…”
Section: Introductionmentioning
confidence: 99%
“…The expression of these genes is responsible for many functions in the organism, such as synthesis of the H blood group antigen [18,19]; synthesis of Lewisx and sialyl-Lewisx antigens [20,21]; addition of fucose to GlcNAc asparagine [22]; and the addition of fucose directly in to polypeptide chains [23]. Thus, this functional property, within the composition of the oligosaccharides, confer to fucose an important role in the health of the immune system.…”
Section: Discussionmentioning
confidence: 99%