• Search Research Projects
  • Search Researchers
  • How to Use
  1. Back to project page

2005 Fiscal Year Final Research Report Summary

Gene Regulation of GATA-4 transcription factor and pathology

Research Project

Project/Area Number 14370744
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypeSingle-year Grants
Section一般
Research Field Biological pharmacy
Research InstitutionOsaka University

Principal Investigator

MAEDA Masatomo  Osaka University, Graduate School of Pharmaceutical Sciences, Professor, 薬学研究科, 教授 (80190297)

Co-Investigator(Kenkyū-buntansha) KOBAYASHI-OHASHI Ayako  Osaka University, Graduate School of Pharmaceutical Sciences, Assistant Professor (Lecturer), 薬学研究科, 講師 (90272484)
Project Period (FY) 2002 – 2005
KeywordsGATA factor / GATA-4 / GATA-6 / cAMP / transcription factor / translational regulation / cardiac myocyte differentiation / proteolysis
Research Abstract

1.Transcription start sites of GATA-4 gene were not significantly different between rat heart, stomach and testis. In the cardiac myocyte differentiation model (mouse P19.CL6 cells), GATA-4 gene was activated, immediately after induction by DMSO. An E-box and two GC-boxes were important for transcription of GATA-4 gene. However, the -124 bp region with these three boxes was not enough for the induced-expression of reporter gene that was constructed by ligating this 124 bp sequence to the 5'-side of GFP gene. Further upstream -125 〜 -1312 bp region together was required for the induced expression.
2.The cAMP-dependent proteolysis occurred in CHO-K1 cells. The potential phosphorylation site by A-kinase and the PEST sequence on the GATA-6 were not required for the proteolysis, and rather other cellular protein(s) could be a target for A-kinase. Thus it would be of interest to identify novel cellular factor(s) functioning in A-kinase pathway.
3.Two translational isoforms (L- and S-types) were formed from a single mRNA, since additional translational initiation codon was present in frame in the further 5'-upstream region of GATA-6 mRNA being not recognized previously. L-type GATA-6 had extended 146 amino acid residues. The 16-residue region in the L-type specific sequence was required for the extended structure of L-type GATA-6. Furthermore, transcriptional activation potency of L-type GATA-6 was higher. Roles of protein factor(s) interacting with the L-type specific region would be interesting from view points of complex formation and transcriptional regulation.
4.Both L- and S-type GATA-6 were expressed in human cancer cell lines. The growth regulation of such cancer cells through GATA-6 would be next study, since we have now known many molecular properties of GATA-6 in the present research project.

  • Research Products

    (10 results)

All 2006 2005 2004

All Journal Article (10 results)

  • [Journal Article] GATA-4 gene organization and analysis of its promoter.2006

    • Author(s)
      Yasunori Ohara
    • Journal Title

      Biol.Pharm.Bull. 29

      Pages: 410-419

    • Description
      「研究成果報告書概要(和文)」より
  • [Journal Article] GATA-4 gene organization and analysis of its promoter.2006

    • Author(s)
      Yasunori Ohara, Takeshi Atarashi, Takuya Ishibashi, Ayako Ohashi-Kobayashi, Masatomo Maeda
    • Journal Title

      Biol.Pharm.Bull. 29

      Pages: 410-419

    • Description
      「研究成果報告書概要(欧文)」より
  • [Journal Article] Characterization of cAMP-dependent proteolysis of GATA-6.2005

    • Author(s)
      Akiko Ishida
    • Journal Title

      Biochem.Biophys.Res.Commun. 332

      Pages: 976-981

    • Description
      「研究成果報告書概要(和文)」より
  • [Journal Article] Further extension of mammalian GATA-6.2005

    • Author(s)
      Masatomo Maeda
    • Journal Title

      Dev.Growth Differ. 47

      Pages: 591-600

    • Description
      「研究成果報告書概要(和文)」より
  • [Journal Article] Isolation of CHO-K1 clones defective in CAMP-dependent proteolysis, as determined by the stability of exogenously expressed GATA-6.2005

    • Author(s)
      Masatomo Maeda
    • Journal Title

      Biochem.Biophys.Res.Commun. 329

      Pages: 140-146

    • Description
      「研究成果報告書概要(和文)」より
  • [Journal Article] Characterization of cAMP-dependent proteolysis of GATA-6.2005

    • Author(s)
      Akiko Ishida, Ryoko Iijima, Ayako Kobayashi, Masatomo Maeda
    • Journal Title

      Biochem.Biophys.Res.Commun. 332

      Pages: 976-981

    • Description
      「研究成果報告書概要(欧文)」より
  • [Journal Article] Isolation of CHO-K1 clones defective in cAMP-dependent proteolysis, as determined by the stability of exogenously expressed GATA-6.2005

    • Author(s)
      Masatomo Maeda, Akiko Ishida, Lin Ni, Masatomo Maeda
    • Journal Title

      Biochem.Biophys.Res.Commun. 329

      Pages: 140-146

    • Description
      「研究成果報告書概要(欧文)」より
  • [Journal Article] Further extension of mammalian GATA-6.2005

    • Author(s)
      Masatomo, Maeda, Kazuaki Ohashi, Ayako Ohashi-Kobayashi
    • Journal Title

      Dev.Growth Differ. 47

      Pages: 591-600

    • Description
      「研究成果報告書概要(欧文)」より
  • [Journal Article] A unique role of an amino terminal 16-residue region of long-type GATA-6.2004

    • Author(s)
      Mika Takeda
    • Journal Title

      J.Biochem. 135

      Pages: 639-650

    • Description
      「研究成果報告書概要(和文)」より
  • [Journal Article] A unique role of an amino terminal 16-residue region of long-type GATA-6.2004

    • Author(s)
      Mika Takeda, Kanako Obayashi, Ayako Kobayashi, Masatomo Maeda
    • Journal Title

      J.Biochem. 135

      Pages: 639-650

    • Description
      「研究成果報告書概要(欧文)」より

URL: 

Published: 2007-12-13  

Information User Guide FAQ News Terms of Use Attribution of KAKENHI

Powered by NII kakenhi