analysis of molecular mechanisms underlying nuclear translocation in migrating neurons
| Project/Area Number |
22700337
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| Research Category |
Grant-in-Aid for Young Scientists (B)
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| Allocation Type | Single-year Grants |
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| Research Field |
Neuroscience in general
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| Research Institution | Kyoto University |
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Principal Investigator |
UMESHIMA Hiroki 京都大学, 物質-細胞統合システム拠点, 研究員 (40525375)
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| Project Period (FY) |
2010-04-01 – 2014-03-31
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| Project Status |
Completed (Fiscal Year 2013)
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| Budget Amount *help |
¥3,900,000 (Direct Cost: ¥3,000,000、Indirect Cost: ¥900,000)
Fiscal Year 2013: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2012: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2011: ¥780,000 (Direct Cost: ¥600,000、Indirect Cost: ¥180,000)
Fiscal Year 2010: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
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| Keywords | 脳・神経 / 発生・分化 / 細胞・組織 |
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| Research Abstract |
Nuclear translocation of migrating neurons is prerequisite for the formation of functional brain circuits, but its molecular mechanism has remained unclear. In this study, I focused on dynamics of the cytoskeleton, which is closely related to nuclear dynamics, and successfully obtained high-resolution time-lapse images of nuclear and cytoskeletal dynamics during nuclear translocation, simultaneously. In addition, we investigated the roles of several cytoskeletal and nuclear proteins for neuronal migration (and nuclear translocation) and I reported that CDK5, a kinase regulating many cytoskeletal proteins, differentially regulates two types of migration of cerebellar granule neurons. This study is expected to help our understanding of neuronal disorders associated with neuronal migration defects.
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Report
(5 results)
Research Products
(7 results)
