Clarification of cell polarity formation mechanism in archenteron formation
| Project/Area Number |
17207015
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| Research Category |
Grant-in-Aid for Scientific Research (A)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Developmental biology
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| Research Institution | National Institute for Basic Biology |
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Principal Investigator |
UENO Naoto National Institute for Basic Biology, Division of Morphogenesis, Professor (40221105)
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| Co-Investigator(Kenkyū-buntansha) |
KINOSHITA Noriyuki National Institute for Basic Biology, Division of Morphogenesis, Associate Professor (30300940)
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| Project Period (FY) |
2005 – 2007
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| Project Status |
Completed (Fiscal Year 2007)
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| Budget Amount *help |
¥48,880,000 (Direct Cost: ¥37,600,000、Indirect Cost: ¥11,280,000)
Fiscal Year 2007: ¥15,990,000 (Direct Cost: ¥12,300,000、Indirect Cost: ¥3,690,000)
Fiscal Year 2006: ¥15,990,000 (Direct Cost: ¥12,300,000、Indirect Cost: ¥3,690,000)
Fiscal Year 2005: ¥16,900,000 (Direct Cost: ¥13,000,000、Indirect Cost: ¥3,900,000)
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| Keywords | cell polarity / Archenteron formation / Xenopus laevis / prickle / spina bifida / 初期発生 / 器官形成 / 再生 / 進化 / 細胞間相互作用 / 遺伝子発現 / 遺伝子機能 / ゲノム |
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| Research Abstract |
Remarkable study results were obtained for the control and the cell polarity formation of the cell migration in the archenteron formation in 2007 fiscal year. Research representative's Ueno identified positive restrictor ANR5 of the cellular adhesion as a negative controlling mechanism of the cell migration. ANR5 was one of the genes identified as a target gene of cellular growth factor FGF ANR5, and clarified that the cellular adhesion was exactly controlled by uniting directly with PAPC and controlling the RhoA revitalization in the downstream by excessive appearance and the functional inhibition that used [moruforinoanchisensuorigonukureochido]. Moreover, ANR5 was necessary for forming a film projection necessary so that the cell may move mutually in the group, and, as a result, it was clarified to play an indispensable role to the archenteron formation (Chung, H. A., et. al., Curr. Biol.). Moreover, Kinoshita, et al. clarified that the cell movement of the archenteron formation was adjusted by cellular growth factor's Wnt acting on the mesoblast cell, and controlling the ubiquitin related resolution of [pakishirin] with an indispensable role to the cell movement (Iioka, H., et. al., Nat Cell Biol.). These are important study results in which it is shown that the movement as the group of the cell is indispensable to the archenteron formation. In addition, Ueno clarified that the analysis that paid attention to the microtubule elongation about the initiation mechanism of a form and functional polarity making about the cell seen when the primitive gut was formed was done, and the boundary of the generation process between paragraphs had the polarity beginning signal (Shindo, A., et. al. PLoS ONE). I want to advance the research on the substance of this polarity beginning signal in the future.
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Report
(4 results)
Research Products
(20 results)
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[Journal Article] Monounsaturated fatty acid modification of Wnt protein : its role in Wnt secretion.2006
Author(s)
Takada, R., Satomi, Y., Kurata, T., Ueno, N., Norioka, S., Kondoh, H., Takao, T., Takada, S.
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Journal Title
Dev. Cell 11
Pages: 791-801
Related Report
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[Journal Article] XGAP, and ArfGAP, is required for polarized localizaton of PAR proteins and cell polarity Xenopus gastrulation2006
Author(s)
Hyodo-Miura, J., Yamamoto, TS., Hyodo, AC., Iemusa, S., Kusakabe, M, Nishida, E., Natsume T., Ueno N.
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Journal Title
Dev. Cell 11
Pages: 69-79
Related Report
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[Journal Article] The initiator caspase, caspase-10beta, and the BH-3-only molecule, Bid, demonstrate evolutionary conservation in Xenopus of their pro-apoptotic activities in the extrinsic and intrinsic pathways.2006
Author(s)
Kominami, K., Takagi, C., Kurata, T., Kitayama, A., Nozaki, M., Sawasaki, T., Kuida, K., Endo, Y., Manabe, N., Ueno, N., Sakamaki K.
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Journal Title
Genes Cells. 11
Pages: 701-717
Related Report
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