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Investigation of the susceptibility gene for COPD by homozygosity fingerprinting method

Research Project

Project/Area Number 18390242
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypeSingle-year Grants
Section一般
Research Field Respiratory organ internal medicine
Research InstitutionSaitama Medical University

Principal Investigator

HAGIWARA Koichi  Saitama Medical University, Faculty of Mecicine, Professor (00240705)

Project Period (FY) 2006 – 2007
Project Status Completed (Fiscal Year 2007)
Budget Amount *help
¥16,770,000 (Direct Cost: ¥15,300,000、Indirect Cost: ¥1,470,000)
Fiscal Year 2007: ¥6,370,000 (Direct Cost: ¥4,900,000、Indirect Cost: ¥1,470,000)
Fiscal Year 2006: ¥10,400,000 (Direct Cost: ¥10,400,000)
KeywordsHomozygosity Fingerprinting / Disease susceptibility gene / GeneChip / Analysis for Identical-by-descent / Autozygous segment / HapMap / Sienificance threshold / COPD / 疾患感受性遺伝子 / ホモ接合ハプロタイプ / SNP / Marfan症候群 / 単因子疾患 / 多因子疾患 / 共通先祖由来断片
Research Abstract

The elucidation of the responsible gene for the multigene diseases is a difficult but an important subject. In this area, the whole genome association approach is frequently employed. However, the method is applicable only to diseases of which frequency is high, and the result often lacks reproducibility. We have invented the Homozygosity Fingerprinting method that targets multigene diseases. It is a non-parametric method applicable to recessive genes. We have determined several parameters for the method using Haldane's Poisson process model for the recombination of the chromosome, and established theoretical background for the identification of recessive genes that are derived from a small number of ancestors and now spread into the population. Using the parameter, we analyzed 6 patients with alpha-1 antitrypsin deficiency, with 45 HapMap Japanese data as a control. Although the 6 patients were from different areas of Japan, we could identify the location of alpha1-antitrypsin gene from their genotyping data. With the use of 1000k GeneChip recently available, we are able to identify genes derived from common ancestors who lived 600 years ago. The method is applicable even to the diseases that are caused by several genes, and thus is considered to be useful for the identification of such genes.
The method has already approved Japanese patent (No. 4059517) and now being transferred to international phase.

Report

(3 results)
  • 2007 Annual Research Report   Final Research Report Summary
  • 2006 Annual Research Report
  • Research Products

    (9 results)

All 2007 2006 Other

All Journal Article (5 results) (of which Peer Reviewed: 4 results) Presentation (2 results) Patent(Industrial Property Rights) (2 results)

  • [Journal Article] Mutanons in the SLC34A2 gene are associated with the pulmonary alveolar microlithiasis.2007

    • Author(s)
      Huqun, et. al.
    • Journal Title

      Am J Respir Crit Care Med 175

      Pages: 263-268

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2007 Final Research Report Summary
    • Peer Reviewed
  • [Journal Article] Homozygosity haplotype allows a genomewide search for the autosomal segment shared among patients2007

    • Author(s)
      Miyazawa, et. al.
    • Journal Title

      American Journal of Human Genetics 80

      Pages: 1090-1102

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2007 Final Research Report Summary
    • Peer Reviewed
  • [Journal Article] Mutations in the SLC34A2 gene are associated with the pulmonary alveolar microlithiasis.2007

    • Author(s)
      Huqun
    • Journal Title

      Am J Respir Crit Care Med 175

      Pages: 263-268

    • Related Report
      2007 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Homozygosity haplotype allows a genomewide search for the autosomalsegment shared among patients2007

    • Author(s)
      Miyazawa
    • Journal Title

      American Journal of Human Genetics 80

      Pages: 1090-1102

    • Related Report
      2007 Annual Research Report
    • Peer Reviewed
  • [Journal Article] The Homozygosity Haplotype allows a genome-wide search for the autosomal segments shared among disease patients

    • Author(s)
      Miyazawa H
    • Journal Title

      American Journal of Human Genetics (In press)

    • Related Report
      2006 Annual Research Report
  • [Presentation] Homozygosity haplotype allows a genomewide search for the autosomal segment shared among patients2007

    • Author(s)
      Miyazawa, et. al.
    • Organizer
      アメリカ人類遺伝学会
    • Place of Presentation
      アメリカSan Diego
    • Year and Date
      2007-10-25
    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      2007 Final Research Report Summary
  • [Presentation] Homozygosity haplotype allows a genomewide search for the autosomalsegment shared among patients.2007

    • Author(s)
      Miyazawa
    • Organizer
      アメリカ人類遺伝学会
    • Place of Presentation
      アメリカSan Diego
    • Year and Date
      2007-10-25
    • Related Report
      2007 Annual Research Report
  • [Patent(Industrial Property Rights)] 特許2007

    • Inventor(s)
      萩原 弘一
    • Industrial Property Rights Holder
      萩原 弘一
    • Acquisition Date
      2007-12-28
    • Related Report
      2007 Annual Research Report
  • [Patent(Industrial Property Rights)] ホモ接合ハプロタイプ法2006

    • Inventor(s)
      萩原弘一
    • Industrial Property Rights Holder
      埼玉医科大学など
    • Industrial Property Number
      2006-214300
    • Filing Date
      2006-08-07
    • Related Report
      2006 Annual Research Report

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Published: 2006-04-01   Modified: 2016-04-21  

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