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Cloning and expression of a porcine UDP-GalNAc: polypeptideN-acetylgalactosaminyl transferase
Authors:Aruto Yoshida   Tomoka Hara   Hiroshi Ikenaga  Makoto Takeuchi
Affiliation:(1) Central Laboratories for Key Technology, Kirin Brewery Co., Ltd, Fukuura, Kanazawa-ku, 236 Yokohama, Japan
Abstract:By employing a bovine UDP-N-acetylgalactosamine: polypeptideN-acetylgalactosaminyl transferase (O-GalNAc transferase) cDNA as a probe, we isolated four overlapping cDNAs from a porcine lung cDNA library. Both the nucleotide sequence of the porcine cDNA and the predicted primary structure of the protein (559 amino acids) proved to be very similar to those of the bovine enzyme (95% and 99% identity, respectively). Transient expression of the clone in COS-7 cells, followed by enzymatic activity assays, demonstrated that this cDNA sequence encodes a porcine O-GalNAc transferase. The intracellular O-GalNAc transferase activity was increased approximately 100-fold by transfecting cells with the porcine cDNA.Abbreviations O-GalNAc transferase UDP-N-acetylgalactosamine: polypeptideN-acetylgalactosaminyltransferase - PCR polymerase chain reaction - SDS sodium dodecyl sulfate - PAGE polyacrylamide gel electrophoresis - GnT-III UDP-N-acetylglucosamine: beta-mannoside beta-1,4N-acetylglucosaminyltransferase III
Keywords:UDP-N-acetylgalactosamine  polypeptideN-acetyl galactosaminyl transferase  glycosyltransferase  O-linked sugars  mucin  porcine
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