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Identification and functional analysis of the transcriptonal complex regulating haematopoiesis

Research Project

Project/Area Number 24790090
Research Category

Grant-in-Aid for Young Scientists (B)

Allocation TypeMulti-year Fund
Research Field Biological pharmacy
Research InstitutionTeikyo University

Principal Investigator

MURATA Takuya  帝京大学, 薬学部, 助教 (00610106)

Project Period (FY) 2012-04-01 – 2014-03-31
Project Status Completed (Fiscal Year 2013)
Budget Amount *help
¥4,550,000 (Direct Cost: ¥3,500,000、Indirect Cost: ¥1,050,000)
Fiscal Year 2013: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2012: ¥2,730,000 (Direct Cost: ¥2,100,000、Indirect Cost: ¥630,000)
Keywords血球分化 / 転写制御 / 遺伝子発現 / 転写共役因子 / 遺伝子発現制御 / 転写 / クロマチン
Research Abstract

To clarify molecular mechanism of C/EBPa transcriptional regulation in granulopoiesis, we tried to identify transcriptional cofactors of C/EBPa. As a result, we identified poly(ADP-ribose) polymerase-1 (PARP-1) as an interactant of C/EBPa. PARP-1 co-represses C/EBPa transcriptional activity and reduces gene expression of C/EBPa target gene, myeloperoxidase (MPO). Additionally, PARP-1 binds C/EBPa response elements region and colocalizes with C/EBPa there. It is supposed that PARP-1 inhibits C/EBPa binding to response element.

Report

(3 results)
  • 2013 Annual Research Report   Final Research Report ( PDF )
  • 2012 Research-status Report
  • Research Products

    (2 results)

All 2013

All Presentation (2 results)

  • [Presentation] Functional analysis in transcriptional regulation of C/EBPa2013

    • Author(s)
      村田拓哉、瀧川遼、高倉勇気、野尻久雄
    • Organizer
      日本分子生物学会
    • Place of Presentation
      神戸ポートアイランド
    • Year and Date
      2013-12-03
    • Related Report
      2013 Final Research Report
  • [Presentation] 血球分化誘導転写因子C/EBPaの転写制御におけるPARP1の機能解析2013

    • Author(s)
      村田拓哉
    • Organizer
      分子生物学会
    • Place of Presentation
      神戸ポートアイランド
    • Related Report
      2013 Annual Research Report

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Published: 2013-05-31   Modified: 2019-07-29  

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