2013 Fiscal Year Final Research Report
Mode of action of Septin-molecular complex
Project/Area Number |
23700463
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Multi-year Fund |
Research Field |
Neurochemistry/Neuropharmacology
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Research Institution | Nagoya University |
Principal Investigator |
SHINODA Tomoyasu 名古屋大学, 医学(系)研究科(研究院), 助教 (80505652)
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Project Period (FY) |
2011 – 2013
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Keywords | 神経発生 / 大脳皮質形成 |
Research Abstract |
Septins are a family of conserved GTP/GDP-binding proteins implicated in a variety of cellular functions such as cell cycle control and cytokinesis. We performed a screening to indentify interacting molecules for Sept4 and Sept14. By using a method combining affinity column chromatography with shotgun liquid chromatography tandem mass spectrometry, we obtained several candidates including Drebrin-1 and Cofilin-1, regulator proteins of actin cytoskeleton. As it was previously reported that Cofilin-1 is involved in cortical neuronal migration, we examined the functional involvement of Drebrin-1 for neuronal migration. Knockdown experiments by in utero electroporation showed that reduction of Drebrin-1 caused inhibition of neuronal migration. Biochemical analyses revealed the direct interaction between Sept4 and Drebrin-1, Sept14 and Cofilin-1, respectively. These results suggest that Sept4-Sept14 complex involved in neuronal migration by regulating the dynamics of actin cytoskeleton.
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[Journal Article] TAG-1-assisted progenitor elongation streamlines nuclear migration to optimize subapical crowding2013
Author(s)
Okamoto M, Namba T, Shinoda T, Kondo T, Watanabe T, Inoue Y, Takeuchi K, Eno moto Y, Ota K, Oda K, Wada Y, Sagou K, Sakakibara A, Kawaguchi A, Nakajima K, Adachi T, Fujimori T, Ueda M, Hayashi S, Kaibuchi K, Miyata T
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Journal Title
Nat. Neurosci.
Volume: 16
DOI
Peer Reviewed
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