2012 Fiscal Year Final Research Report
Does TOR related factors control the cell division mode and the morphogenesis in developing embryo?
Project/Area Number |
21590195
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
General anatomy (including Histology/Embryology)
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Research Institution | Meiji University of Integrative Medicine (2011-2012) Kyushu University (2009-2010) |
Principal Investigator |
HIROSE Eiji 明治国際医療大学, 医学教育研究センター, 准教授 (40380620)
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Co-Investigator(Kenkyū-buntansha) |
NARUSE Yoshihisa 明治国際医療大学, 医学教育研究センター, 准教授 (00326216)
NAKAJO Nobushige 九州大学, 理学研究院, 助教 (90294876)
KOJIMA Takuya 東京大学, 農学生命科学研究院, 助教 (90346312)
INAI Tetsuichiro 福岡歯科大学, 基礎医歯学部門, 教授 (00264044)
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Project Period (FY) |
2009 – 2012
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Keywords | アフリカツメガエル / 線虫 / マウス / TOR / RagGTPase |
Research Abstract |
We isolated the RagGTPase family genes and mapped their spatial and temporal expression pattern in the developing embryo. We also analyzed the effects of the gene defects such as gene deletion or the translation blockage on the cell division mode in the developing embryo. The expression of two RagGTPase genes showed unique pattern, and the expression ratio of these two genes were drastically changed in the developing stage. This ratio changing of two genes suggested to switch the two cell division modes during the embryonic development. The one is a rapid cell division mode in nutrient-rich condition (early embryonic cell division with sufficient york), and another is slow cell division mode in nutrient-poor condition (late embryonic cell division or starved animal).
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Research Products
(17 results)
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[Journal Article] Dynamic regulation of Emi2 by Emi2-bound Cdk1/Plk1/CK1 and PP2A-B56 in meiotic arrest of Xenopus eggs.2011
Author(s)
Isoda M, Sako K, Suzuki K, Nishino K, Nakajo N, Ohe M, Ezaki T, Kanemori Y, Inoue D, Ueno H, Sagata N.
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Journal Title
Dev Cell.
Volume: 21(3)
Pages: 506-19
Peer Reviewed
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