Molecular Cloning of Siaα2,3Galβ1,4GlcNAc α2,8-Sialyltransferase from Mouse Brain

A cDNA encoding a new α2,8-sialyltransferase (ST8Sia III), which exhibits activity toward the Siaα2,3Galβ1,4GlcNAc sequences of N-linked oligosaccharides, was cloned from mouse brain by means of the polymerase chain reaction-based approach. The predicted amino acid sequence of ST8Sia III showed 27.6...

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Veröffentlicht in:The Journal of biological chemistry 1995-06, Vol.270 (24), p.14628-14633
Hauptverfasser: Yoshida, Yukiko, Kojima, Naoya, Kurosawa, Nobuyuki, Hamamoto, Toshiro, Tsuji, Shuichi
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Sprache:eng
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Zusammenfassung:A cDNA encoding a new α2,8-sialyltransferase (ST8Sia III), which exhibits activity toward the Siaα2,3Galβ1,4GlcNAc sequences of N-linked oligosaccharides, was cloned from mouse brain by means of the polymerase chain reaction-based approach. The predicted amino acid sequence of ST8Sia III showed 27.6 and 34.4% identity with those of so far cloned mouse α2,8-sialyltransferases, i.e. GD3 synthase (ST8Sia I) and STX (ST8Sia II), respectively. Transfection of the protein A-fused ST8Sia III gene into COS-7 cells led to α2,8-sialyltransferase activity toward sialylated glycoproteins and α2,3-sialylated glycosphingolipids, such as α2,3-sialylparagloboside and GM3. However, the kinetic properties of ST8Sia III revealed that it is much more specific to N-linked oligosaccharides of glycoproteins than glycosphingolipids. The expression pattern of the ST8Sia III gene was clearly different from those of other α2,8-sialyltransferase genes. The expression of the ST8Sia III gene was tissue and stage specific. The ST8Sia III gene was expressed only in brain and testis, and it appeared first in 20 postcoitum embryonal brain and then decreased. Therefore, the new α2,8-sialyltransferase is closely involved in brain development.
ISSN:0021-9258
1083-351X
DOI:10.1074/jbc.270.24.14628