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Studies on the mechanism on the neuron specific gene expression.

Studies on the mechanism on the neuron specific gene expression.
神经元特异性基因表达机制的研究。
批准号:
63044091
负责人:
MIKOSHIBA Katsuhiko
金额:
$2.43万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Overseas Scientific Survey.
财政年份:
1988
资助国家:
日本
项目状态:
已结题
起止时间:
1988 至 1989

项目摘要

项目成果

MIKOSHIBA Katsuhiko的其他基金

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相关文献

中文摘要
翻译
鞭毛系统中存在多种细胞,具有不同的特征功能。这些细胞中的大多数从共同的祖先神经上皮细胞分化而来,迁移到它们定义的位置,形成组织良好的神经系统结构。作为了解这些过程中涉及的分子机制的第一步,我们一直在识别调节神经细胞中特定产生的蛋白质的基因表达的元件。少突胶质细胞标志蛋白髓磷脂碱性蛋白和星形胶质细胞标志蛋白胶质纤维酸性蛋白基因明显被类核因子-1元件(S)激活,而神经元特异性蛋白神经丝基因似乎被下调。髓鞘蛋白脂蛋白(PLP)在空间和时间上与MBP相似,但其基因表达的调控机制似乎与MBP基因截然不同。因此,神经细胞以各种方式激活基因,可能是因为每个基因的表达都必须对环境变化做出精细的反应,才能展示神经系统的复杂功能。
英文摘要
Many kinds of cells are present in the vervous system and exhibit various characteristic functions. Most of these cells differentiate from a common ancestor, neuroepithelial cells, migrate to their defined positions, and form well-organized architecture of the nervous system. As a first step toward understanding molecular mechanisms involved in these processes, we have been identifying the elements which regulate the gene expression of the proteins specifically produced in the neural cells. The genes for myelin basic protein (MBP), an oligodendrocyte marker protein, and glial fibrally acidic protein, an astrocyte marker protein, were apparently activated by NF-1 like element(s), while the gene for neurofilament, a neuron-specific protein, seemed to be de-repressed in neuron. Myelin proteolipid protein (PLP) is produced spacially and timely similar to MBP, however, the regulatory mechanism involved in its gene expression seemed to be quite distinct from that of the MBP gene. Thus, the neural cells activate the genes in various ways, presumably because each gene expression has to finely respond to the environmental change in order to exhibit the complex functions of the nervous system.
期刊论文(20)
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科研奖励(0)
会议论文
田村隆明ら: "Tissue-specific in vitro transcription from the mouse myelin basic protein promoter." Mol.Cell.Biol.9. 3122-3126 (1989)
Takaaki Tamura 等人:“小鼠髓磷脂碱性蛋白启动子的组织特异性体外转录。”Mol.Cell.Biol.9 (1989)。
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通讯作者:
Tamura, Taka-aki: "Enhance of human polyoma JC virus contains nuclear factor I-binding sequences; analysis using mouse brain nuclear extracts." Biochem. Biophys. Res. Comm.157. 419-425 (1988)
Tamura, Taka-aki:“人类多瘤 JC 病毒的增强包含核因子 I 结合序列;使用小鼠脑核提取物进行分析。”
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田村隆明ら: "Analysis of transcription control elements of the mouse myelin basic protein gene in HeLa cell extrancts:Demonstration of a strong NF1-binding motif in the upstream region." Nucl.Acid Res.16. 11441-11459 (1988)
Takaaki Tamura 等人:“HeLa 细胞提取物中小鼠髓磷脂碱性蛋白基因的转录控制元件的分析:上游区域中强 NF1 结合基序的演示。Nucl.Acid Res.16(1988 年)” )
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通讯作者:
Ikenaka, Kazuhiro: "Myelin proteolipid protein gene structure and its regulation of expression in normal and jimpy mutant mice." J. Mol. Biol.199. 587-596 (1988)
Ikenaka、Kazuhiro:“髓磷脂蛋白脂质蛋白基因结构及其在正常和 jimpy 突变小鼠中的表达调节。”
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共 20 条
    Study of IP_3 receptor/Ca^<2+> signaling in neural plasticity and brain development and differentiation
    Study of IP3 receptor/Ca^<2+> signaling in neural plasticity and brain development and differentiation
    Study for IP_3 - detecting system of IP_3 receptor
    • 批准号:
      13357001
    • 项目类别:
      Grant-in-Aid for Scientific Research (A)
    • 资助金额:
      $31.78万
    • 财政年份:
      2001
    • 负责人:
      MIKOSHIBA Katsuhiko
    • 依托单位:
    Role of IP_3 receptor/ Ca^<2+> signaling for synaptic plasticity and development and differentiation of brain
    • 批准号:
      13308044
    • 项目类别:
      Grant-in-Aid for Scientific Research (A)
    • 资助金额:
      $29.2万
    • 财政年份:
      2001
    • 负责人:
      MIKOSHIBA Katsuhiko
    • 依托单位:
    海外基金