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Study on Ganglioside GM3 Synthase and Its Gene.

Research Project

Project/Area Number 10670109
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field General medical chemistry
Research InstitutionNational Cancer Center Research Institute

Principal Investigator

ISHII Atushi  National Cancer Center Research Institute, Virology and Glycobiology Division, Section Chief, ウイルス部, 室長 (20232225)

Co-Investigator(Kenkyū-buntansha) SAITO Masaki  National Cancer Center Research Institute, Virology and Glycobiology Division, Chief, ウイルス部, 部長 (60012762)
Project Period (FY) 1998 – 2000
Project Status Completed (Fiscal Year 2000)
Budget Amount *help
¥3,300,000 (Direct Cost: ¥3,300,000)
Fiscal Year 2000: ¥700,000 (Direct Cost: ¥700,000)
Fiscal Year 1999: ¥900,000 (Direct Cost: ¥900,000)
Fiscal Year 1998: ¥1,700,000 (Direct Cost: ¥1,700,000)
KeywordsGM3 synthase / transcriptional promoter / Sp1 / Genomic organization / NFY / Targetting mice / GH3合成酵素 / ゲノムDNA / 抗体 / ガングリオシドGM3 / シアル酸転移酵素 / HL-60細胞 / 分化誘導療法
Research Abstract

We recently cloned a human cDNA for ganglioside GM3 synthase. Elucidation of the mechanisms controlling expression of the GM3 synthase gene is very important and interesting, since the enzyme is only α2, 3-sialyltransferase capable of the biosynthesis of ganglioside GM3. Firstly, we isolated a BAC clone containing an entire human GM3 synthase gene and analyzed its organization. Human GM3 synthase gene spans approximately 54 kbps of genomic DNA with seven exons, ranging from 112 to 1,242 bp, and six intron. FISH analysis revealed gene is located near the centromere of the about arm on chromosome 2, an area which corresponds to band 2p11.2. To identify the promoter region of the gene, about 10 kbp fragment containing 5'-flanking region and a part of exon 1 of the gene was subcloned into promoter-less luciferase plasmid. Deletion analyses indicated that the region from nt -285 to nt +103 is essential for full promoter activity. Furthermore, mutation analyses showed that two Sp1 sites and one NFY site are important for positive transcriptional regulation of the gene. Next, we cloned cDNA homologs from mice, rat and monkey to explore the structure-function relationship of GM3 synthases. Mouse, rat and monkey GM3 synthases to human homolog were 85.0%, 84.8% and 97.6% identical, respectively, at the nucleic acid level. Mouse GM3 synthase gene which was mapped to chromosome 6, region C on mouse genome, spans approximately 58 kbps of genomic DNA with nine exons, ranging from 112 to 1,172 bp, and eight intron. Different from that of the human GM3 synthase gene, the mechanisms of an alternative splicing and alternative promoter utilization were involved in the expression of mouse GM3 synthase gene, resulting the production of 3 transcript variants with different 5'-end sequences. We tried to the generation of GM3 synthase targetting mice to analyze the function of ganglioside GM3 and more complex gangliosides in individual. Now we obtained chimeric mice.

Report

(4 results)
  • 2000 Annual Research Report   Final Research Report Summary
  • 1999 Annual Research Report
  • 1998 Annual Research Report
  • Research Products

    (7 results)

All Other

All Publications (7 results)

  • [Publications] Ishii A. et al.: "Expression Cloning and Functional Characterization of Human cDNA for Ganglioside GM3 Synthase"Journal of Biological Chemistry. 273. 31652-31655 (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] 石井睦,齋藤政樹: "糖鎖生物学"共立出版. 2349-2357 (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Saito M.and Ishii A.: "Handbook of Glycosyl transferases"Springer-Verlag,NY.(印刷中).

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Ishii A., et al.: "Expression cloning and Functional Characterization of Human cDNA for Ganglioside GM3 Synthase."J.Biol. Chem.. 273. 31652-31655 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Ishii A.and Saito M.: "Structure and Function of GM3 synthetic sialyltransferase. Glycobiology"Kyouritsu Press Inc., Tokyo Japan. 9 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Saito, M.and Ishii, A.: "ST3GalV (Ganglioside GM3 Synthase), Handbook of Glycosyltrans-Ferases"Springer-Verlag (in press).

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2000 Final Research Report Summary
  • [Publications] Atsushi Ishii et al.: "Expression cloning and Functional Characterization of Human cDNA for Ganglioside GM3 Synthesis" Journal of Biological Chemistry. 273. 31652-31655 (1998)

    • Related Report
      1998 Annual Research Report

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Published: 1998-04-01   Modified: 2016-04-21  

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