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2001 Fiscal Year Final Research Report Summary

Impact of mutations and polymorphisms in transporter families on population health

Research Project

Project/Area Number 12470081
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypeSingle-year Grants
Section一般
Research Field Hygiene
Research InstitutionKYOTO UNIVERSITY

Principal Investigator

KOIZUMI Akio  Kyoto. Univ., Medicine, Professor, 医学研究科, 教授 (50124574)

Co-Investigator(Kenkyū-buntansha) YOSHINAGA Takeo  Kyoto.Univ., Medicine, Associate Prof., 医学研究科, 助教授 (30025663)
Project Period (FY) 2000 – 2001
Keywordsmutations / transporters / LPI / SLC7A7 / R410X / Osler-Rendu-Weber / polycystic / proinsulin
Research Abstract

Transporters play crucial roles in transporting biological substances. We have focused our attention to the effects of mutations of transporters on population health.
1. Lysinuric protein intolerance (LPI) was a disease caused by a mutation of basic amino acid transporter SLC7A7. LPI is controllable by early intervention at infancy. It is endemic in Iwate while its prevalence is very small in other areas in Japan. Its early intervention, therefore, is one of the public health issues specific to Iwate. We conduced genetic epidemiological study and had shown a founder mutation of R41OX mutation in SLC7A7. Excess prevalence of LPI was attributed to a high gene frequency of this founder mutation.
2. We embarked a mass screening program using molecular diagnosis for LPI. The mass screening program turned out to be cost effective and reliable as a diagnosis tool.
3. We also conducted genetic epidemiology in a local cluster of Osler-Rendu-Weber disease, polycystic Kidney and a local goiter unknown pathogenesis.
4. We tried to evaluate functionally the mutated proteins in an attempt to develop a general methodology to predict ftinctional alterations. In this project, we evaluated mutations of proinsulin Akita as-an example.
The prevalences of genetic diseases are very widely perturbed by the population history and social systems. It is necessary to promote research activities for genetic epidemiology and functional proteomics.

  • Research Products

    (27 results)

All Other

All Publications (27 results)

  • [Publications] Kubota T.: "Probable involvement of a germ-line mutation of an unknown mismatch repair gene in a Japanese Muir-Torre sundrome phenotype"J. Dermatol. Sci.. 23. 117-125 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Habuchi T.: "Association of Vitamin F recptor gene polymorphisms with prostata cancer and benign prostatic hyperplasia in a Japanese population"Cancer Res.. 60. 305-308 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Noguchi A.: "SLC7A7 gemonic structure and novel variants in three Japanese lysinuric prootein intolerance families"Human Mutation. 15. 367-372 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Kayo T.: "A Identification of two chromosomal Loci determining glucose intolerance in a C57BL/6 mouse strain"Comparative Medicine. 50. 296-302 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Koizumi A.: "Excesive clustring of lysinuric protein intolerance (LP1) patinets in a nothermn part of Japan due to a founder effect"Hum. Mutation. 16. 270-270 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Shioya T.: "Hereditary hemorrhagic telangiectasia (HHT) in Akita Prefecture, Japan"Int. Med.. 39. 675-676 (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Takahashi T.: "A new locus for a dominant form of multinodular goiter on 3q26.1-q26.3"Biochem. Biophys. Res. Commun.. 284. 650-654 (2001)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Nozaki J.: "Homozygosity mapping to chromosome 5p15 of a gene responsible for Hartnup disorder"Biochem. Biophys. Res. Commun.. 284(2). 255-260 (2001)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Abe T.: "Suppression of experimental autoimmune uveoretinitis by dietary calorie restriction"Jpn. J. Ophthalmol.. 45・1. 46-52 (2001)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Fujita H.: "An increased Expression of Glutathione S-Transferases in the Renal Proximal Tubuli in the Early Stage of Diabetes : a Study in a Mouse Model of Type 2 Diabetes, Akita"Exp. Nephrol.. 9. 380-386 (2001)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Dakeishi M.: "Genetic epidemiology of hereditary hemorrhagic telagioectasia in a ocalcommunity in the northern part of Japan"Human Mutation. 19. 149-158 (2002)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Seiichi Oyadomari: "A targeted disruption of The CHOP gene protects mice against ER stress-induced diabetes"J. Clin. Invest.. 109. 525-532 (2002)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Inoue S.: "Mutation Analysis of PKD1 in Japanese Autosomal Dominant Polycystic Kidney Disease (ADPKD) Patients"Human Mutation. (in press). (2002)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] 小泉 昭夫(分担): "公衆衛生学"放送大学出版. (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Kubota T.: "Probable involvement of a germ-line mutation of an unknown mismatch repair gene in a Japanese Muir-Torresundrome Phenotype"J. Dermatol. Sci.. 23. 117-125 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Habuchi T.: "Association of Vitamin F. recptor gene polymorphisms with prostata cancer and benign prostatic hyperplasia in a Japanese population"Cancer Res.. 60. 305-308 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Noguchi A: "SLC7A7 gemonic structure and novel variants in three Japanese lysinuric proolein into lerance families"Human Mutation. 15. 367-3727 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Kayo T.: "Identification of two chromosonal Loci determining glucose intolerance in a C57BL/6 mouse strain"Comparative Medicine. 50. 296-302 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Koizumi A.: "Excesive clustring of lysinuric protein in tolerance (ILP) patinets in a nothermn part of Japan due to a founder effect"Hum Mutat. 16. 270-1 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Shioya T.: "Herditary hemorrhagic telangiectasia (HHT) in Akita Prefecture"Japan Int Med. 39. 675-676 (2000)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Takahashi T.: "A new locus for a dominant form of multinodular goiter on 3q26. 1-q26. 3"Biochem Biophys Res Commun. 284. 650-654 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Nozaki J: "Homozygosity mapping to chromosome 5p15 of a gene responsible for Hartnup disorter."Biochem Biophvs Res Commur. 284(2). 255-60 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Abe T.: "Suppression of experimental autoitaime uveoretiriitis by dietary calorie restriction"Jpn J Ophthalmol Jan-Feb. 45(1). 46-52 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Fujita H: "An Increased Expression of Glutathione S-Transferases in the Renal Proximal Tubuli in the Early Stage of Diabetes : a Study-in a Mouse Model of Type 2 Diabetes, Akita Mouse"Exp Nephrol. 9. 380-386 (2001)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Dakeishi M: "Genetic epidemiology of hereditary hemorrhagic telagioectasia in a localcommunity in the northern part of Japan"Human Mut. 19. 149-148 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Seiichi Oyadomari: "A targeted disruption of The CHOP gene protects mice against ER stress-induced diabetes"J Clin Invest.. 109. 525-532 (2002)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Inoue S: "Mutation Analysis of PKD1 in Japane Autosomal Dominant Polycystic Kidney Disease (ADPKD) Patients"Human Mutation. (in press).

    • Description
      「研究成果報告書概要(欧文)」より

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Published: 2003-09-17  

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