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Ablation of Mina53 in mice reduces allergic response in the airways

Research Project

Project/Area Number 21570204
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Cell biology
Research InstitutionTakasaki University of Health and Welfare

Principal Investigator

TSUNEOKA Makoto  高崎健康福祉大学, 薬学部, 教授 (50197745)

Co-Investigator(Kenkyū-buntansha) UMATA Toshiyuki  産業医科大学, 産業医学研究支援施設, 准教授 (30213482)
Project Period (FY) 2009 – 2011
Project Status Completed (Fiscal Year 2011)
Budget Amount *help
¥4,810,000 (Direct Cost: ¥3,700,000、Indirect Cost: ¥1,110,000)
Fiscal Year 2011: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2010: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2009: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
KeywordsMina53 / アレルギー / リボソーム / 喘息 / IL4 / 気道過敏性 / 炎症性細胞浸潤 / 遺伝子 / 核酸 / 細胞・組織 / KDM2A / リボソームRNA / コハク酸 / ピストン脱メチル化酵素 / 転写 / JmjC / MINA
Research Abstract

Asthma is a highly prevalent chronic respiratory disease affecting 300 million people world-wide. Allergic asthma is the most common form of asthma, a Th2-biased disease, and triggered by inhaling allergens such as house dust mites(HDM). In addition to the environmental factors, genetic factors are also involved in asthma. However, the interaction of these factors is complex and not fully understood. It was recently reported that Mina53 was a necessary and sufficient dose-dependent IL-4-specific 'repressor' in naive helper T cells, using an ex vivo system of Th2-differentiation from naive helper T cells(Nat Immunol. 2009 ; 10 : 872-9). However, there have been no experiments investigating the role of Mina53 in the Th2-bias in vivo in animals. While it had been reported that Mina53(myc-induced nuclear antigen with a 53 kDa molecular mass ; also known as mina) is associated with tumorigenesis, it was not clear what role Mina53 plays in non-neoplastic tissues. To directly address the functions of Mina53 in a normal body, we created mina53-deficient mice. While both male and female mina53-deficient mice grew to adulthood and were fertile, we found that Mina53 functions as an 'activator' in the allergic response, in asthma, possibly through controlling IL-4 production. We also analyzed the effect of succinate on ribosome biogenesis, and found that succinate inhibited another JmjC protein KDM2A to increase the rDNA transcription.

Report

(4 results)
  • 2011 Annual Research Report   Final Research Report ( PDF )
  • 2010 Annual Research Report
  • 2009 Annual Research Report
  • Research Products

    (16 results)

All 2012 2011 2010 2009 Other

All Journal Article (6 results) (of which Peer Reviewed: 5 results) Presentation (8 results) Remarks (2 results)

  • [Journal Article] JmjC enzyme KDM2A is a regulator of rRNA transcription in response to starvation2010

    • Author(s)
      Tanaka Y., Tanaka Y, Okamoto K, Teye K, Umata T, Yamagiwa N, Suto Y, Zhang Y, Tsuneoka M
    • Journal Title

      EMBO J

      Volume: 29(9) Pages: 1510-22

    • Related Report
      2011 Final Research Report
  • [Journal Article] JmjC enzyme KDM2A is a regulator of rRNA transcription in response to starvation.2010

    • Author(s)
      Yuji Tanaka
    • Journal Title

      EMBO J.

      Volume: 29 Pages: 1510-1522

    • Related Report
      2010 Annual Research Report
    • Peer Reviewed
  • [Journal Article] mina53, a novel c-Myc target gene, is frequently expressed in lung cancers and exerts oncogenic property in NIH/3T3 cells2010

    • Author(s)
      Kazutoshi Komiya
    • Journal Title

      J Cancer Res Clin Oncol 136

      Pages: 465-73

    • Related Report
      2009 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Expression of Mina53, a novelc-Myc target gene, is a favorable prognostic marker in early stage lung cancer2010

    • Author(s)
      Kazutoshi Komiya
    • Journal Title

      Lung Cancer (掲載決定印刷中)

    • Related Report
      2009 Annual Research Report
    • Peer Reviewed
  • [Journal Article] Accelerated expression of a Myc target gene Mina53 in aggr essive hepatocellular carcinoma2010

    • Author(s)
      Sachiko Ogasawara
    • Journal Title

      Hepatol Res. 40

      Pages: 330-336

    • Related Report
      2009 Annual Research Report
    • Peer Reviewed
  • [Journal Article] JmjC enzyme KDM2A is a regulator of rRNA transcription in response to starvation2010

    • Author(s)
      Yuji Tanaka
    • Journal Title

      EMBO J. 29

      Pages: 1510-1522

    • Related Report
      2009 Annual Research Report
    • Peer Reviewed
  • [Presentation] ヒストン修飾酵素KDM2AによるリボソームRNA転写調節2012

    • Author(s)
      常岡誠、田中祐司、岡本健吾
    • Organizer
      第1回リボソームミーティングで
    • Place of Presentation
      広島
    • Year and Date
      2012-03-15
    • Related Report
      2011 Final Research Report
  • [Presentation] Histone demethylase KDM2A reduces rRNA transcription in response to starvation2011

    • Author(s)
      常岡誠、田中祐司、岡本健吾
    • Organizer
      第32回分子生物学学会ワークショップ
    • Place of Presentation
      横浜
    • Year and Date
      2011-12-16
    • Related Report
      2011 Annual Research Report 2011 Final Research Report
  • [Presentation] ヒストン脱メチル化酵素KDM2Aによるクロマチン構造調節とリボソームRNA転写2011

    • Author(s)
      常岡誠
    • Organizer
      遺伝研研究会
    • Place of Presentation
      三島
    • Year and Date
      2011-10-20
    • Related Report
      2011 Annual Research Report 2011 Final Research Report
  • [Presentation] ヒストン脱メチル化酵素によるリボソームRNA転写制御2011

    • Author(s)
      常岡誠
    • Organizer
      日本生化学会関東支部例会
    • Place of Presentation
      東京新宿
    • Year and Date
      2011-06-25
    • Related Report
      2011 Final Research Report
  • [Presentation] ヒストン脱メチル化酵素によるリボソームRNA転写制御2011

    • Author(s)
      常岡誠
    • Organizer
      日本生化学会関東支部会例会
    • Place of Presentation
      東京新宿
    • Year and Date
      2011-06-25
    • Related Report
      2011 Annual Research Report
  • [Presentation] ヒストン脱メチル化酵素KDM2AによるリボソームRNA発現調節2011

    • Author(s)
      常岡誠
    • Organizer
      転写研究会・若手シンポジウム
    • Place of Presentation
      東京
    • Year and Date
      2011-02-18
    • Related Report
      2010 Annual Research Report
  • [Presentation] 脱メチル化酵素KDM2A(jumonji-C containing histone demethylase 1A)によるリボソームRNA転写の調節2010

    • Author(s)
      田中祐司
    • Organizer
      第33回日本分子生物学会年会
    • Place of Presentation
      神戸(一般口頭発表)
    • Year and Date
      2010-12-09
    • Related Report
      2010 Annual Research Report
  • [Presentation] 脱メチル化酵素KDM2Aは飢餓状態でリボソームRNA転写を抑制する2009

    • Author(s)
      田中祐司
    • Organizer
      分子生物学会
    • Place of Presentation
      横浜
    • Year and Date
      2009-12-12
    • Related Report
      2009 Annual Research Report
  • [Remarks]

    • URL

      http://www.takasaki-u.ac.jp/yaku2/idenshikinouseigyo/toppage.htm

    • Related Report
      2011 Final Research Report
  • [Remarks]

    • URL

      http://www.takasaki-u.ac.jp/yaku2/idenshikinouseigyo/toppage.htm

    • Related Report
      2011 Annual Research Report

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Published: 2009-04-01   Modified: 2016-04-21  

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