2014 Fiscal Year Final Research Report
Mechanisms underlying determination of positional information through Dachsous/Fat signaling system
Project Area | Molecular mechanisms underlying reconstruction of 3D structers during regeneration |
Project/Area Number |
22124003
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Research Category |
Grant-in-Aid for Scientific Research on Innovative Areas (Research in a proposed research area)
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Allocation Type | Single-year Grants |
Review Section |
Biological Sciences
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Research Institution | The University of Tokushima |
Principal Investigator |
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Co-Investigator(Kenkyū-buntansha) |
OHUCHI Hideyo 岡山大学, 医歯(薬)学総合研究科, 教授 (00253229)
MITO Taro 徳島大学, 大学院ソシオテクノサイエンス研究部, 助教 (80322254)
BANDO Tetsuya 岡山大学, 医歯(薬)学総合研究科, 助教 (60423422)
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Project Period (FY) |
2010-04-01 – 2015-03-31
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Keywords | 脚再生 / Dachsous/Fat / Wnt/BMP/EGF / dachshund/Distal-less / マクロファージ / Enhancer of zeste/Utx / ゲノム編集 / ノックイン |
Outline of Final Research Achievements |
We have investigated molecular mechanisms underlying insect leg regeneration by means of regeneration-dependent RNA interference. Our results suggested that leg regeneration occurs as follows: (1) Activation of macrophage-like cells by amputation at the amputated site, (2) Cytokines produced by the macrophage-like cells induce formation of a blastema consisting of undifferentiated cells, (3) In the blastema, EGF (epidermal growth factor) is induced by cross-talk of Wnt/BMP signaling pathways. Furthermore, genes involved in epigenetic regulations such as Enhancer of Zest and Utx are activated, (4) EGF induces expressions of dachshund/Distal-less and regulates expression of Dachsous/Fat signaling systems, which then determine re-patterning of the leg and its size. We speculated that the leg size regulation may be related to the number of Dachsous/Fat molecules in each cell membrane with a proximodistal gradient. This was simulated with our modified steepness model.
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Free Research Field |
再生生物学
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