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Study on the tissue specific expression of phosphatidylinositol synthase and its function.

Research Project

Project/Area Number 09680612
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Functional biochemistry
Research InstitutionGunma University

Principal Investigator

HOSAKA Kohei  Gunma University, Faculty of Medicine, Professor, 医学部, 教授 (70108992)

Project Period (FY) 1997 – 1998
Project Status Completed (Fiscal Year 1998)
Budget Amount *help
¥3,400,000 (Direct Cost: ¥3,400,000)
Fiscal Year 1998: ¥800,000 (Direct Cost: ¥800,000)
Fiscal Year 1997: ¥2,600,000 (Direct Cost: ¥2,600,000)
Keywordsin situ hybridization / mRNA / phosphatidylinositol synthase / distribution in brain / cell cycle / inhibitor / cyclinD / cyclinE / ラット / ホスファチジルイノシトール / ホスファチジルイノシトール合成酵素 / G1期 / サイクリンD / サイクリンE / リン脂質 / インサイトハイブリダゼイーション / mRNA / 海馬
Research Abstract

Phosphatidylinositol synthase (PIS) catalyzes the formation of phosphatidylinositol (Pl) from myo-inositol and CDP-diacylglyceol and mediates the final step in the biosynthetic sequence leading to phosphoinositide. We have recently isolated and characterized a PIS cDNA from rat brain. The results obtained by this project are follows :
i) In situ hybridization histochemistry revealed that PIS mRNA is selectively expressed in neuron-rich regions of the adult rat brain, such as cerebral cortex, hippocampus, thalamus, hypothalamus, and spinal cord. By contrast, little to no hybridization signal was observed in white matter-rich areas such as the corpus callosum. The expression of PIS mRNA was determinated during pre- and postnatal development of the rat central nervous system. On embryonic day 18, PIS was expressed mainly neuron-enriched areas such as cortical plate and ventricular zone whereas little to no mRNA is detected in glia-enriched areas.
ii) Quantitative reverse transcription-polymerase chain reaction analysis as well as in situ hybridization showed that the PIS transcript level dramatically increased during the first postnatal week, and peaked at 7-14 days after birth.
iii) Since the preliminary results suggested the presence of a new isoform of PIS, I tried to clone the isoform with several methods. But the new clone could not be isolated.
iv) Dr. Umezawa(Keio Univ.) reported that inostamycin, known as a specific inhibitor of Pl synthesis, blocked both the Pl synthesis and G1 progression in the serum stimulated rat fibroblast cells. The collaboration study with him revealed that another inhibitor, delta- hexachlorocyclohexane, also blocked the both activity as inostamycin. Furthermore the blockade was due to the inhibition of the expression cyclin D and cyclin E.These results suggest that P13 plays an important role in cell cycle.

Report

(3 results)
  • 1998 Annual Research Report   Final Research Report Summary
  • 1997 Annual Research Report
  • Research Products

    (10 results)

All Other

All Publications (10 results)

  • [Publications] A.Na Kashima, K.Hosaka and J.Nikawa: "Clonirg 4 a human coil for CTP-phosphoethanolamine Cytidylyltransferage by complementation in vivo of a yeast mutant." J.Biol.Chem.272. 9567-9572 (1997)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] H.Imai etal: "Dfferentel distribution of mRAIAs encoding phusphatidylinostop transta paterns α and βin the central nervous system of the rat." Mol.BrainRes.46. 256-254 (1997)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] S.kagiwada, K.Hosaka 他 3名: "The Saaharo myus cerevisiae SCS2 gene product, a homolog of a synatobrurn-associated protein, 25an integral mombnene prokm of fliendu bsmieritzwlum and is neguiie for inosufel 〓" J.Baeferiol.180. 1700-1708 (1998)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] A.Nakashima, K.Hosaka and J.Nikawa: "Cloning of a human cDNA for CTP-phosphoethanolamine cytidyltransferase by complementation in vivo of a yeast mutant" J.Biol.Chem.272. 9567-9572 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] H.Imai, S.Tanaka, T.Fukusato, S.Yamashita and K.Hosaka: "Differential distribution of mRNAs encoding phosphatidylinositol transfer proteins alpha and beta in the centralnervous system of the rat." Mol.Brain Res.46. 256-254 (1997)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] S.Kagiwada, K.Hosaka, M.Murata, J.Nikawa and A.Takatsuki: "The Saccharomyces cerevisiae SCS2 gene product, a homolog of a synaptobrevin-associated protein, is an integral membrane protein of the endoplasmic reticulum and is required for inositol metabolism." J.Bacteriol.180. 1700-1708 (1998)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1998 Final Research Report Summary
  • [Publications] S. Kagiwada,K. Hosaka他3名: "The Saccharomyes conev : Sial SCS2gen ploduct,ahomolg of a synaptobrevn-associated proter,zs an integral membrau patein of the endo plgore retiulum and Sgequred forsutl mefab" J. Baeteriol.180. 1700-1708 (1998)

    • Related Report
      1998 Annual Research Report
  • [Publications] Satoshi Yamashita & Kohei Hosaka: "Cholin Rinase from yeast" Biochim,Biophys,Acta. 1384. 63-69 (1997)

    • Related Report
      1997 Annual Research Report
  • [Publications] Hideshi Iwai他4名: "Differentcal distrbution of mRNA emoding phosphatidyl inasrtaltrancfor proteins α and β in the central nernois system of the rat" Mol.Brain Res.46. 256-264 (1997)

    • Related Report
      1997 Annual Research Report
  • [Publications] Asae Nakashima, Kohei Hosaka & Jan-chi Nikawa: "Cloning of a Human cDNA for CTP-phosphcefthanolamine Stidylyltrnng-feraic by complementation in vioo of a yeast mutant" J.Biol.Chem.272. 9567-9572 (1997)

    • Related Report
      1997 Annual Research Report

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Published: 1997-04-01   Modified: 2016-04-21  

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