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The research for the susceptibility genes of multifactorial genetic disease applied bottom-up proteomics

Research Project

Project/Area Number 25460703
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeMulti-year Fund
Section一般
Research Field Laboratory medicine
Research InstitutionNihon University

Principal Investigator

NAKAYAMA Tomohiro  日本大学, 医学部, 教授 (00339334)

Co-Investigator(Kenkyū-buntansha) KUBOTA Takeo  山梨大学, 総合研究部医学, 教授 (70293511)
NOMURA Fumio  千葉大学, 医学(系)研究科(研究院), 教授 (80164739)
Project Period (FY) 2013-04-01 – 2016-03-31
Project Status Completed (Fiscal Year 2015)
Budget Amount *help
¥5,070,000 (Direct Cost: ¥3,900,000、Indirect Cost: ¥1,170,000)
Fiscal Year 2015: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2014: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2013: ¥2,210,000 (Direct Cost: ¥1,700,000、Indirect Cost: ¥510,000)
Keywords遺伝性疾患 / プロテオミクス / 感受性遺伝子 / 疾患マーカー / 遺伝子 / 塩基配列決定法
Outline of Final Research Achievements

We have collected the seventy-eight samples with essential hypertension, cerebral infarction, myocardial infarction, diabetes. After getting a written consent, we extracted genomic DNA from white blood cells. We inspected participants whether they have family history of the disorders by hearing exact information about family careers. The clinical data such as sex, age, family history, height, weight, body mass index, total cholesterol, triglyceride, HDL cholesterol, uric acid, blood sugar, urine acids, electrocardiogram, a smoking history, drinking career. The DNA samples were stocked in deep freezers until analysis, and the isolated plasma were analyzed for proteomics analysis by the MALDI-TOF MS.
A next-generation sequencer was used for the genomics analysis especially for exome analysis. In addition, Sanger method was applied for the individual genetic analysis. SNPAlyze software was used for haplotype-based case-control study.

Report

(4 results)
  • 2015 Annual Research Report   Final Research Report ( PDF )
  • 2014 Research-status Report
  • 2013 Research-status Report
  • Research Products

    (3 results)

All 2015 Other

All Journal Article (1 results) Presentation (2 results)

  • [Journal Article] 日本総合健診医学会 第43回大会 大会講演 シンポジウム1 遺伝子診断の現状と未来「分析の質の担保」。2015

    • Author(s)
      中山智祥
    • Journal Title

      総合健診42(3):396-402. 2015.6

      Volume: 42 Pages: 396-402

    • Related Report
      2015 Annual Research Report
  • [Presentation] Gitelman症候群の塩基配列決定法およびMultiplex Ligation-dependent Probe Amplification: MLPA法2015

    • Author(s)
      中山智祥、鳴瀬 弘
    • Organizer
      第60回日本人類遺伝学会大会
    • Place of Presentation
      京王プラザホテル(東京都、新宿区)
    • Year and Date
      2015-10-14
    • Related Report
      2015 Annual Research Report
  • [Presentation] SMTN遺伝子と本態性高血圧症とのハプロタイプを用いた関連解析

    • Author(s)
      中山智祥
    • Organizer
      第36回 日本分子生物学会年会
    • Place of Presentation
      神戸
    • Related Report
      2013 Research-status Report

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Published: 2014-07-25   Modified: 2019-07-29  

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