Study on the tissue specific expression of phosphatidylinositol synthase and its function.
| Project/Area Number |
09680612
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Functional biochemistry
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| Research Institution | Gunma University |
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Principal Investigator |
HOSAKA Kohei Gunma University, Faculty of Medicine, Professor, 医学部, 教授 (70108992)
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| Project Period (FY) |
1997 – 1998
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| Project Status |
Completed (Fiscal Year 1998)
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| 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)
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| Keywords | in 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 |
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| 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.
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Report
(3 results)
Research Products
(10 results)
