Cloning and expression of a human gene encoding an N-acetylgalactosamine-α2,6-sialyltransferase (ST6GalNAc I): a candidate for synthesis of cancer-associated sialyl-Tn antigens

The sialyl-Tn (sTn) antigen is a well known cancer-associated antigen, the expression of which is related to the prognosis of cancer patients. We aimed to isolate a human gene encoding an N-acetylgalactosamine α2,6-sialyltransferase which synthesizes sTn antigen, and to characterize the enzyme. Dege...

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Published inGlycobiology (Oxford) Vol. 9; no. 11; pp. 1213 - 1224
Main Authors Ikehara, Yuzuru, Kojima, Naoya, Kurosawa, Nobuyuki, Kudo, Takashi, Kono, Mari, Nishihara, Shoko, Issiki, Soichiro, Morozumi, Kyoei, Itzkowitz, Steven, Tsuda, Tetsuro, Nishimura, Shin-Ichiro, Tsuji, Shuichi, Narimatsu, Hisashi
Format Journal Article
LanguageEnglish
Published Oxford University Press 01.11.1999
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Summary:The sialyl-Tn (sTn) antigen is a well known cancer-associated antigen, the expression of which is related to the prognosis of cancer patients. We aimed to isolate a human gene encoding an N-acetylgalactosamine α2,6-sialyltransferase which synthesizes sTn antigen, and to characterize the enzyme. Degenerate primers encoding sialyl motifs were used for the polymerase chain reaction to amplify complementary DNAs prepared from RNAs of human pyloric mucosae with intestinal metaplasia, which abundantly expressed sTn antigen, followed by screening of full-length cDNAs using the amplified DNA fragment as a probe. We isolated two human cDNA clones, long-form (2.46 kb) and short-form (2.23 kb) cDNAs. The former encodes an active enzyme with a predicted 600 amino acid sequence. The latter, a splice-variant of the long-form, encodes an inactive enzyme. HCT15 human colorectal cancer cells stably expressing the long-form cDNA expressed sTn epitopes on O-glycans. The long form cDNA was considered to encode a human homologue of chick ST6GalNAc I for the following reasons: (1) the putative amino acid sequence showed greater homology to that of chick ST6GalNAc I (55%) compared to other sialyltransferases, (2) it encodes the extraordinarily long stem region that is a typical feature of chick ST6GalNAc I, and (3) the substrate specificity was very similar to that of chick ST6GalNAc I. In situ hybridization demonstrated that the localization of transcripts correlated well with that of sTn antigen in gastric cancer cells and Goblet cells in intestinal metaplastic glands. Thus, we determined that the long-form cDNA of the human ST6GalNAc I gene encodes the probable candidate for the human sTn synthase(s).
Bibliography:4To whom correspondence should be addressed at: Division of Cell Biology, Institute of Life Science, Soka University, 1-236 Tangi-cho, Hachioji, Tokyo 192-8577
ark:/67375/HXZ-8X3MBV5S-6
Present address: Laboratory of Pathology, Aichi Cancer Center Research Institute, Chikusa-ku, Nagoya 464-0021, Japan
istex:DF11CA3B120FA835126CE70B1307585F97A666A3
ISSN:0959-6658
1460-2423
DOI:10.1093/glycob/9.11.1213