Molecular mechanism of vascular system formation
血管系统形成的分子机制
基本信息
- 批准号:10304063
- 负责人:
- 金额:$ 23.87万
- 依托单位:
- 依托单位国家:日本
- 项目类别:Grant-in-Aid for Scientific Research (A).
- 财政年份:1998
- 资助国家:日本
- 起止时间:1998 至 2000
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
1. Analysis with Arabidopsis vascular mutants, van1-van7 : Molecular analysis of Arabidopsis vascular mutants, van1-van7 with a pAthb8-GUS or pTED3-GUS fusion gene revealed that defects of these mutants were caused by abnormal pattern formation of procambial cells. In addition, we displayed that the continuity of the vascular network is more sensitive to genetic lesions than their overall architecture is, supporting the diffusion-reaction prepattern model.2. Analysis of the HD-Zip homeobox genes during carrot somatic embryogenesis. We analyzed expression pattern of 6 HD-Zip homeobox genes, CHB1-CHB6, with in situ hybridization during carrot somatic embryogenesis, and revealed that all the genes were expressed in association with vascular cells in the late stage of embryogesesis, that is, CHB6 was expressed specifically in procambium and others were in different vascular cells. These results suggest that the HD-Zip homeobox genes are involved in vascular formation.3. Analysis of vascula … More r cell differentiation with an in vitro Zinnia system in which mesophyll cells differentiate into vascular cells.(1) We revealed the presence of different kind of vascular cells in the in vitro Zinnia culture system.(2) We established new culture methods, with which a tracheary element-inducing factor was partially purified. The partially purified substance was a high molecular weight-arabinogalactan protein and designated "xylogen".(3) We found that brassinosteroids were synthesized prior to Stage 3 of differentiation and their biosynthesis was regulated by a coordinated increase in transcription of genes encoding brassinosteroid biosynthesis. In addition, our finding that castasterone, an active brassinosteroid, is secreted preferentially out of the cell and accumulates in medium, suggests that brassinosteroids function at extracellular surface of the cell.(4) Using a phage display subtraction method, we succeeded in isolating of three novel antibodies recognizing cell walls of specific vascular cells. Less
1。拟南芥血管突变体的分析,VAN1-VAN7:拟南芥血管突变体的分子分析,带有PathB8-GUS或PTED3-GUS融合基因的VAN1-VAN7 vAN1-VAN7揭示了这些突变体的缺陷,是由异常模式形成引起的。此外,我们表明,血管网络的连续性对遗传病变的敏感性比其整体结构更敏感,从而支持扩散反应的预生产模型2。胡萝卜体细胞胚发生过程中HD-ZIP同源基因的分析。我们分析了6个HD-ZIP同源基因CHB1-CHB6的表达模式,并在胡萝卜体细胞胚胎发生过程中具有原位杂交,并揭示了所有基因在胚胎的后期与血管细胞相关表达,即CHB6在Procambium和其他不同的血管细胞中特异性表达。这些结果表明,HD-ZIP同源基因基因与血管形成有关3。对血管的分析…与体外Zinnia系统的更多R细胞分化,其中叶叶叶叶细胞分化为血管细胞。(1)我们揭示了体外Zinnia培养系统中存在不同种类的血管细胞。(2)我们建立了新的培养方法,通过这种气管元素诱导的因子是部分含有纯化的。部分纯化的物质是一种高分子量 - 阿拉伯分泌蛋白,并指定为“木基生成”。(3)我们发现,在分化的第3阶段之前,在基因的转录增加了编码铜氨基固醇生物合理的基因的转录中,在分化的第3阶段之前合成了铜氨基固醇。此外,我们的发现,即castasterone是一种活性的胸腺固醇,更优选地分泌出细胞,并在培养基中积聚,这表明铜氨基固醇在细胞的细胞外表面上起作用。(4)使用噬菌体显示减法方法,我们成功地隔离了三种新型抗体识别特定血管细胞的细胞壁的新型抗体。较少的
项目成果
期刊论文数量(52)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Fukuda,H.: "Programmed cell death of tracheary elements as a paradigm in plants."Plant Mol.Biol.. 44. 245-253 (2000)
Fukuda, H.:“气管元件的程序性细胞死亡作为植物的范例。”Plant Mol.Biol.. 44. 245-253 (2000)
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- 影响因子:0
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Endo,S.: "Inhibition of proteasome activity by the TED4 protein in extracellular space : a novel mechanism for protection of living cells from injury caused by dying cells."Plant Cell Physiol.. 42. 9-19 (2001)
Endo,S.:“细胞外空间中 TED4 蛋白对蛋白酶体活性的抑制:一种保护活细胞免受死亡细胞损伤的新机制。”植物细胞生理学.. 42. 9-19 (2001)
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Tokuji, Y: "A rapid method for transformation of carrot (Daucus carota L.) by using direct somatic embryogenesis"Biosci. Biotechnol. Biochem.. 63. 519-523 (1999)
Tokuji, Y:“通过使用直接体细胞胚胎发生来快速转化胡萝卜 (Daucus carota L.) 的方法”Biosci。
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- 影响因子:0
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Fukuda, H., Watanabe, Y., Kuriyama, H., Aoyagi, S, Sugiyama, M., Yamamoto, R, Demura, T., Minami, A.: "Programming of Cell Death during Xylogenesis."J.Plant Res.. 111. 253-256 (1998)
Fukuda, H.、Watanabe, Y.、Kuriyama, H.、Aoyagi, S、Sugiyama, M.、Yamamoto, R、Demura, T.、Minami, A.:“木质生成过程中细胞死亡的编程。”J.Plant
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Sugiyama, M., Ito, J., Aoyagi, S.and Fukuda, H.: "Endonuclease."Plant Mol.Biol.. 44. 387-397 (2000)
Sugiyama, M.、Ito, J.、Aoyagi, S. 和 Fukuda, H.:“核酸内切酶”。植物分子生物学 44. 387-397 (2000)
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FUKUDA Hiroo其他文献
FUKUDA Hiroo的其他文献
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{{ truncateString('FUKUDA Hiroo', 18)}}的其他基金
Analysis of phloem function as a signaling center
韧皮部作为信号中心的功能分析
- 批准号:
20247003 - 财政年份:2008
- 资助金额:
$ 23.87万 - 项目类别:
Grant-in-Aid for Scientific Research (A)
Comprehensive identification and analysis of extracellular signaling molecules involved in vascular tissue formation
全面鉴定和分析参与血管组织形成的细胞外信号分子
- 批准号:
17207004 - 财政年份:2005
- 资助金额:
$ 23.87万 - 项目类别:
Grant-in-Aid for Scientific Research (A)
Molecular basis of induction and execution of programmed cell death in plants
植物程序性细胞死亡诱导和执行的分子基础
- 批准号:
15370018 - 财政年份:2003
- 资助金额:
$ 23.87万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Studies of cell-cell communication during vascular formation
血管形成过程中细胞间通讯的研究
- 批准号:
13440236 - 财政年份:2001
- 资助金额:
$ 23.87万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Molecular Basis of Axis and Signals in Plant Development
植物发育中轴和信号的分子基础
- 批准号:
13052101 - 财政年份:2001
- 资助金额:
$ 23.87万 - 项目类别:
Grant-in-Aid for Scientific Research on Priority Areas
Molecular mechanism of the acquirement and restriction of differentiation potency in plant cells
植物细胞分化能力获得和限制的分子机制
- 批准号:
07454215 - 财政年份:1995
- 资助金额:
$ 23.87万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Development of a Three dimensional Skill-Analyzing System by means of "360 Degree Turning of a Motion Model" and Completion of a New Teaching Method Based upon It.
利用“运动模型360度翻转”开发三维技能分析系统并完成基于该系统的新教学方法。
- 批准号:
05558021 - 财政年份:1993
- 资助金额:
$ 23.87万 - 项目类别:
Grant-in-Aid for Developmental Scientific Research (B)
Analysis of irreversible process of cell differntiation in higher plants
高等植物细胞分化不可逆过程分析
- 批准号:
04454011 - 财政年份:1992
- 资助金额:
$ 23.87万 - 项目类别:
Grant-in-Aid for General Scientific Research (B)
Analysis of the mechanism of tracheary-element differentiation using gene transfer techniques
利用基因转移技术分析气管元件分化机制
- 批准号:
02640517 - 财政年份:1990
- 资助金额:
$ 23.87万 - 项目类别:
Grant-in-Aid for General Scientific Research (C)
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