Molecular mechanisms which control the cell movements during ascidian neural tube formation
Molecular mechanisms which control the cell movements during ascidian neural tube formation
批准号:
15570182
负责人:
NISHIKATA Takahito
金额:
$2.3万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2003
资助国家:
日本
项目状态:
已结题
起止时间:
2003 至 2006
中文摘要
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英文摘要
Ascidian neural tube has basically the same structure as those of vertebrates. Its relatively simple structure and the abundant molecular resources of the ascidian offer an excellent experiment system for analyzing the molecular mechanisms of neural tube formation. However, according to our previous studies, the question has been raised as to whether or not the molecular mechanisms of vertebrate and ascidian neural tube formation are similar. So we reexamined the following two subjects.1.Reexamination of Ciona intestinalis Cadherin genes (CiCadI and CiCadII)We have already showed the neural-tube specific expression of CiCadII. We tried to analyze the spatial and temporal expression pattern of the other Ciona classic cadherin, Cadherin type I (CiCadI). Using the RT-PCR, CiCadI expressed maternally and its zygotic expression was detected from gastrula stage to the tailbud stage. This result suggested that, during the Ciona development, the two classic cadherin were used in the neural tube formation. The result that both CiCadI and CiCadII were used during the ascidian neural tube formation suggested the similarity in the molecular mechanisms of the ascidian and vertebrates neural tube formation.2.Reexamination of the cell movement during neural tube formationDuring the vertebrate neural tube formation, two types of mechanisms, primary-and secondary-neural tube formation, are proposed. In this study, we stained cortical actin network with phalloidin, and marked the neural tube cells, which carried GFP-reporter gene driven by the neural-tube specific promoter. The nerve-cord precursor cells actively moved posteriorly and made obvious cell rearrangement. On the other hand, brain-precursor cells did not move much along the anterior-posterior axis. The brain-stem precursor cells contained a certain amount of actin network. These regional differences suggested the different mechanism for each region within the neural tube.
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超実践バイオ実験イラストレイテッド レッスン2 遺伝子実験ステップアップ
超级实用生物实验图解第2课基因实验进阶
DOI:
--
发表时间:
2006
期刊:
影响因子:
--
作者:
[西方敬人, 真壁和裕]
通讯作者:
真壁和裕
UV-irradiated cells as a screening system for the antioxidants
紫外线照射的细胞作为抗氧化剂的筛选系统
DOI:
--
发表时间:
2006
期刊:
Proceedings of the 13th Biennial Congress of the International Society for Free Radical Research -SFRR
影响因子:
--
作者:
[Nishikata, T.]
通讯作者:
T.
超実践バイオ実験イラストレイテッドレッスン2 遺伝子実験ステップアップ
超级实用生物实验图解第2课基因实验进阶
DOI:
--
发表时间:
2006
期刊:
影响因子:
--
作者:
[西方敬人, 真壁和裕]
通讯作者:
真壁和裕
CiYB1 is a major component of storage mRNPs in ascidian oocytes : Implications in mRNA localization and translational regulation.
CiYB1 是海鞘卵母细胞中储存 mRNP 的主要成分:对 mRNA 定位和翻译调控的影响。
DOI:
--
发表时间:
2004
期刊:
Developmental Biology 272
影响因子:
--
作者:
[Tanaka, K.J.]
通讯作者:
K.J.
Shoguchi, E.: "Fluorescent in situ Hybridization to Ascidian Chromosomes."Zoological Science. 21. 153-157 (2004)
Shoguchi, E.:“海鞘染色体荧光原位杂交。”动物学。
DOI:
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发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
共 11 条
Establishment of the loss-of-function experimental system using the maxizyme in the ascidian embryo.
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批准号:13680812
-
项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.11万
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财政年份:2001
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负责人:NISHIKATA Takahito
-
依托单位:
Establishment of the loss-of-function experimental system using the maxizyme in the ascidian embryo.
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批准号:11680728
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.3万
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财政年份:1999
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负责人:NISHIKATA Takahito
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依托单位:
海外基金