Mechanism of fore-mid-brain determination by XSa1F
| Project/Area Number |
17300107
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Neuroscience in general
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| Research Institution | RIKEN |
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Principal Investigator |
SASAI Yoshiki RIKEN, Organogenesis and Neurogenesis Group, Group Director, 細胞分化・器官発生研究グループ, グループデイレクター (20283616)
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| Project Period (FY) |
2005 – 2006
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| Project Status |
Completed (Fiscal Year 2006)
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| Budget Amount *help |
¥14,900,000 (Direct Cost: ¥14,900,000)
Fiscal Year 2006: ¥7,200,000 (Direct Cost: ¥7,200,000)
Fiscal Year 2005: ¥7,700,000 (Direct Cost: ¥7,700,000)
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| Keywords | Neural development / patterning / early embryo / Xenopus / XSa1F / XTsh3 / Wnt / anterior-posterior axis / 神経分化 / 脳発生 / 前脳 / 中脳 / Sal / 転写因子 / Tsh3 |
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| Research Abstract |
The aim of this study is to understand molecular mechanisms of the early vertebrate embryo, particularly in the nervous system, by focusing on the roles of zinc-finger proteins and their related molecules in the rostral neuroectodermal development of Xenopus. We had previously isolated the zinc-finger factor XSa1F, which plays an essential role in the determination of the rostral brain. In this study, we identified another zinc-finger transcription factor, XTsh3, which is expressed in the Xenopus caudal nervous system. We showed that XTsh3 is a promoting factor required for the proper development of the caudal neural tissues. Overexpression of XTsh3 caused caudalization of the neural tissues and suppressed forebrain development. Conversely, XTsh3-MO injection, which blocks its function, enhanced forebrain development. In signaling analysis, we found that XTsh3 augments Wnt/b-catenin signaling. XTsh3 binds to both b-catenin and Tcf3, and amplifies Wnt-induced transcription. Consistent with these observations, XTsh3-MO injection into mesoendodermal tissues inhibited dorsal development, leading to strong ventralization of the whole embryo. Thus, in addition to XSa1F, which acts as a negative modulator of Wnt signaling, XTsh3 plays an important role in the fine modulation of the Wnt pathway. The antagonistic pair of XSa1F and XTsh3 is likely to function as a binary switching system of Wnt-On vs.-Off regulations.
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Report
(3 results)
Research Products
(21 results)
