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Analyses of transcriptional regulation and function of NPAT gene which shares a promoter witn ATM gene.

Research Project

Project/Area Number 10680532
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field 環境影響評価(含放射線生物学)
Research InstitutionNational Institute of Radiological Sciences

Principal Investigator

SAGARA Masashi  NIRS, Genome Res., Researcher, 第2研究グループ, 研究員 (30291107)

Co-Investigator(Kenkyū-buntansha) IMAI Takashi  NIRS, Genome Res., Sub-Group Leader, 第2研究グループ, サブグループリーダー (50183009)
NINOMIYA Yasuharu  NIRS, Genome Res., Researcher, 第2研究グループ, 研究員 (70300910)
Project Period (FY) 1998 – 1999
Project Status Completed (Fiscal Year 1999)
Budget Amount *help
¥3,400,000 (Direct Cost: ¥3,400,000)
Fiscal Year 1999: ¥1,200,000 (Direct Cost: ¥1,200,000)
Fiscal Year 1998: ¥2,200,000 (Direct Cost: ¥2,200,000)
KeywordsNPAT / ATM / bi-directional promoter / CRE / NLS / GFP / bi-directional / ルシフェラーゼ / ゲルシフト
Research Abstract

NPAT is identified as a gene closely linked to the ATM gene. Because these two genes are transcribed in opposite directions and share a 0.5kb 5' upstream sequence, we have investigated the mechanism regulating the expression of ATM and NPAT genes. A reporter assay revealed that the 0.5kb nucleotide sequence flanked by two genes had bi-directional promoter activity, and that the region that was important for transcriptional activation of each gene were different. Moreover, site-directed promoter mutagenesis and electrophoretic mobility shift assays (EMSA) indicate that the CRE-like site and E2F-like sites are important for expression of both genes. We also have shown that the unknown factor different from transcription factors, such as CREB, bind to the CRE-like site.
Next, the NPAT gene product is presumed nuclear protein, because three elements in which four serial basic amino acids presumed to be nuclear localization signals at the carboxyl end domain exists. When analysis of the elements were performed using GFP, it became clear that NPAT gene product is nuclear protein and that all elements are required for localization at nuclear. Moreover, it was shown clearly that it is functioning as a new nuclear localization signal also about the 20 amino acid element of the internal domain of the NPAT gene product.

Report

(3 results)
  • 1999 Annual Research Report   Final Research Report Summary
  • 1998 Annual Research Report
  • Research Products

    (4 results)

All 2002 1999 Other

All Journal Article (2 results) Book (1 results) Publications (1 results)

  • [Journal Article] Characterization of functional regions for nuclear localization of NPAT.2002

    • Author(s)
      Masashi Sagara, et al.
    • Journal Title

      Journal of Biochemistry 132

      Pages: 875-879

    • NAID

      10010653960

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Journal Article] Characterization of functional regions for nuclear localization of NPAT.2002

    • Author(s)
      Sagara M., et al.
    • Journal Title

      Journal of Biochemistry 132-6

      Pages: 875-879

    • NAID

      10010653960

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Book] 細胞周期と癌 p53、RB、チェックポイント制御の新展開1999

    • Author(s)
      今井高志
    • Total Pages
      179
    • Publisher
      羊土社
    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1999 Final Research Report Summary
  • [Publications] 今井高志: "細胞周期と癌p53、RBチェックポイント制御の新展開"羊土社. 179 (1999)

    • Related Report
      1999 Annual Research Report

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Published: 1998-04-01   Modified: 2016-04-21  

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