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Quantitative analysis for transcriptional alteration of glycosyltransferases in colon cancer

Research Project

Project/Area Number 13671340
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Digestive surgery
Research InstitutionKeio University

Principal Investigator

WATANABE Masahiko  Keio University School of Medicine, Lecturer, 医学部, 講師 (80146604)

Co-Investigator(Kenkyū-buntansha) ISSHIKI Soichiro  Keio University School of Medicine, Assistant, 医学部, 助手 (10276264)
Project Period (FY) 2001 – 2002
Project Status Completed (Fiscal Year 2002)
Budget Amount *help
¥1,200,000 (Direct Cost: ¥1,200,000)
Fiscal Year 2002: ¥1,200,000 (Direct Cost: ¥1,200,000)
Keywordsglycosyltransferase / colon cancer / galactosyltransferase
Research Abstract

The type 1 carbohydrate chain,Gal β 1-3GlcNAc,is synthesized by UDP-galactose:β-N-acetylglucoamine β 1,3-galactosyltransferase (β 3Gal-T). Among six β 3Gal-Ts cloned to date, β 3Gal-T5 is an essential enzyme for the synthesis of type 1 chain in epithelium of digestive tracts or pancreatic tissue. It forms the type 1 structure on glycoproteins produced from such tissues. In the present study,we found that the transcriptional regulation for β 3Gal-T5 gene is controlled by homeoproteins, i.e. members of Cdx and hepatocyte nuclear factor (HNF) families. We found an important region (-151~-121 from the transcription initiation site),named the β 3Gal-T5 control element(GCE), for the promoter activity. GCE contained the consensus sequences for members of Cdx and HNF families. Mutations introduced into this sequence abolished the transcriptional activity. Four factors,Cdx1,Cdx2,HNF1 α and HNF1 β,could bind to GCE and transcriptionally activated the β 3Gal-T5 gene
Transcriptional regulation of the β3Gal-T5 gene was consistent with that of the members of Cdx and HNF1 families in two in vivo systems,i.e.1) During in vitro differentiation of Caco-2 cells, transcriptional up-regulation of β 3Gal-T5 was observed in correlation with the increase in transcripts for Cdx2 and HNF1 α. 2) Both transcript and protein of β 3Gal-T5 were determined to be significantly down-regulated in cancerous tissue of colon cancer patients. This down-regulation was correlated with the decrease of Cdx1 and HNF1 β expression in cancer tissue
This is the first finding that a glycosyltransferase gene is transcriptionally regulated under control of homeoproteins in a tissue-specific manner. β 3Gal-T5,controlled by the intestinal homeoproteins, may play an important role for the specific function of intestinal cells by modifying the carbohydrate structure of glycoproteins

Report

(3 results)
  • 2002 Annual Research Report   Final Research Report Summary
  • 2001 Annual Research Report
  • Research Products

    (2 results)

All Other

All Publications (2 results)

  • [Publications] 一色聡一郎, 渡邊昌彦ほか: "大腸におけるルイス1型糖鎖合成酵素(β3Gal-T5)の発現制御"日本分子腫瘍マーカー研究会誌. 16. 62-63 (2001)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2002 Final Research Report Summary
  • [Publications] S, Isshiki, M, Watanabe et al.: "Expression of Lewis type 1 synthase(β3Gal-T5)in colon was regulated by homebox proteins"Journal of Japan Society for Molecular Tumor Marker Research. Vol.16. 62-63 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      2002 Final Research Report Summary

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Published: 2002-04-01   Modified: 2016-04-21  

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