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A novel form of angiokeratoma corporis diffusum: Elucidatim of abnormal metabolites in urine and enzyme defect.

Research Project

Project/Area Number 02454279
Research Category

Grant-in-Aid for General Scientific Research (B)

Allocation TypeSingle-year Grants
Research Field Dermatology
Research InstitutionKagoshima University (1992)
Nagoya City University (1990-1991)

Principal Investigator

KANZAKI Tamotsu  Kagoshima University faculty of Medicine, Professor, 医学部, 教授 (80118801)

Co-Investigator(Kenkyū-buntansha) HIRABAYASHI Yoshio  The Institute of Physical and Chemical Research(RIKEN), Sugar-Information, Chief, 国際フロンティア糖情報部門, 主任研究員 (90106435)
Project Period (FY) 1990 – 1992
Project Status Completed (Fiscal Year 1992)
Budget Amount *help
¥5,900,000 (Direct Cost: ¥5,900,000)
Fiscal Year 1992: ¥700,000 (Direct Cost: ¥700,000)
Fiscal Year 1991: ¥1,500,000 (Direct Cost: ¥1,500,000)
Fiscal Year 1990: ¥3,700,000 (Direct Cost: ¥3,700,000)
KeywordsAngiokeratoma / Lysosomal storage disease / alpha-N-acetylgalactosaminidase / Kanzaki disease / Schindler disease / Molecular analysis / Point mutation / ライソゾーム蓄積症 / びまん性体幹被角血管腫 / αーNーアセチルガラクトサミニデ-ス / ライソゾ-ム蓄積症 / シンドラ-病 / ポイントミュ-テ-ション
Research Abstract

A novel form of angiokeratoma corporis diffusum was discovered in a Japanese female. Abnormal metabolites were detected in the patient's urine and those were reveald to be O-limked glycoaminoacids. From these chemical formula, this novel lysosomal storage disease, now termed Kanzaki disease, was revealed to be caused by an enzyme deficit, ie, alpha-N-acetylgalactosaminidase. ALL these were elucidated in the past a few years in this project. We tried to elucidate a possible defect in the gene encoding this enzyme protein in the last one year.
As a result, it was found that a base at the 985th was switched C to T resulting in a change of amino acid of arginine to tryptophane at 329th. This gene was transfected to COS-1 cell and a new protein was observed to be produced by COS-1 cell. This protein reacted with an antibody to the enzyme but did not show an enzymatic activity. Secondly, a computer-assisted two-dimensional molecular structure was studied and it showed that an change of amino acid induced a secondary change from beta-pleated sheet to random coil. this was quit different from the change observed in Schindler disease, i,e., alpha-helix formation. This change was thought to be the cause of susceptibility of these resultant abnormal enzyme proteines to proteases in lysosomes. This will explain the great differences in the phenotypical expression in the patients with Kanzaki disease and Schindler disease (Wang, A,M. Kanzaki, T. and Desnick,R.J.). These results obtained in this year will be published in Archives of Dermatology (in press,1993) and were submitted to other journals.
Thus, all research works, from the discovery to the molecular analysis of a noval lysosomal storase disease with angiokeratoma corporis diffusum (Kanzaki), planned in this project were successfully accomplished in these years.

Report

(4 results)
  • 1992 Annual Research Report   Final Research Report Summary
  • 1991 Annual Research Report
  • 1990 Annual Research Report
  • Research Products

    (14 results)

All Other

All Publications (14 results)

  • [Publications] Kanzaki,T.,Yokota,M.,Irie,F.,Hirabayashi,Y.,Wang,A.M.and Desnick,R.J.: "Angiokeratoma corporis diffusum with glycopeptiduria due to deficient lysosomal α-N-acetylgalactosaminidase activity:Clinical,morphologic and biochemical studies" Arch.Dermatol. (1993)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1992 Final Research Report Summary
  • [Publications] Wang,A.M.,Kanzaki,T.and Desnick,R.J.: "The molecular lesion in the α-N-acetylgalactosaminidase gene that causes angiokeratoma corporis diffusum with glycopeytiduria" J.Clim.Invest.(1993)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1992 Final Research Report Summary
  • [Publications] 神崎 保: "被角血管腫と代謝異常" 皮膚病診療. (1993)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1992 Final Research Report Summary
  • [Publications] Kanzaki, T. Yokota, M. Irie,F. Hirabayashi, Y. Wang,A.M. and Desnick,R.J.: "Angiokeratoma corporis diffusum with glycopeptiduria due to deficient lysosomal alpha-N-acetylgalactosaminidase activity: Clinical,morphologic and biochemical studies" Arch. Dermatol. (1993)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1992 Final Research Report Summary
  • [Publications] Wang,A.M. Kanzaki, T. and Desnick, R.J.: "The molecular lesion in the alpha-N-acetylgalactosaminidase gene that causes angiokeratoma corporis diffusum with glycopeytiduria" J. Clin. Invest.

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1992 Final Research Report Summary
  • [Publications] Kanzaki, T.: "Angiokeratoma and abnormal metabolism (Japanese)" Hifubyo-Shinryo. (1993)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1992 Final Research Report Summary
  • [Publications] Kanzaki,T. Yokota,M. Irie,F. Hirabayashi,Y. Wang.A.M. and Desnick,R.J.: "Angiokeratoma corporis diffusum with glycopeptiduria due to deficient lysosomal α-N-acetylgalactosaminidase activity:Clinical,morphologic and biochemical studies" Arch.Dermatol. (1993)

    • Related Report
      1992 Annual Research Report
  • [Publications] Wang,A.M. Kanzaki,T. and Desnick,R.J.: "The molccular lcsion in the α-N-acctylgalactosaminidase gene that causcs angiokcratoma corporis diffusum with glycopcytiduria" J.Clin.Invest.(1993)

    • Related Report
      1992 Annual Research Report
  • [Publications] 神崎 保: "被角血管腫と代謝異常" 皮膚病診療. (1993)

    • Related Report
      1992 Annual Research Report
  • [Publications] 神崎 保: "Angiokeratoma類と腎変化" 皮膚病診療. 12. 1009-1012 (1990)

    • Related Report
      1991 Annual Research Report
  • [Publications] 平林 義雄: "び漫性被角血管腫を伴った新しいリソゾ-ム蓄積症の臨床的、生化学的研究" 日本先天代謝異常学会雑誌. 7. 53-57 (1991)

    • Related Report
      1991 Annual Research Report
  • [Publications] Hirabayashi,Y.: "Isolation and characterization of major urinary amino acid Oーglycosides and a dipeptide Oーglycoside from a novel lysosomal storage diserder (Kanzaki disease)." J.Biol.Chem.265. 1693-1701 (1990)

    • Related Report
      1990 Annual Research Report
  • [Publications] Schindler,D.: "A method for the rapid detection of urinary glycopeptides in αーNーacetylgalactosaminidase deficiency and other lysosomal storage disease." Clin.Chim.Acta. 190. 81-92 (1990)

    • Related Report
      1990 Annual Research Report
  • [Publications] Hirabayashi,Y.: "Defects in the metabolism of the Oーlinked oligosaccharides of glycoproteins." T.I.G.G.93-99 (1990)

    • Related Report
      1990 Annual Research Report

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Published: 1990-04-01   Modified: 2016-04-21  

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