Transcription Factors Involved in the induction of Jasmonate-Primary Responsive Gene in Plant Cells
植物细胞中参与诱导茉莉酸初级反应基因的转录因子
基本信息
- 批准号:10460038
- 负责人:
- 金额:$ 10.18万
- 依托单位:
- 依托单位国家:日本
- 项目类别:Grant-in-Aid for Scientific Research (B)
- 财政年份:1998
- 资助国家:日本
- 起止时间:1998 至 1999
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Transcription of the gene for ornithine decarboxylase (ODC) of tobacco BY-2 cells is activated even in the presence of an inhibitor of protein synthesis. A nuclear gene for ODC isolated from tobacco did not contain intron, and the fusion gene composed of the ODC promoter and the GUS reporter gene (ODC : GUS) showed early response to MeJA in transformed tobacco BY-2 cells. Although expression of the ODC: GUS fusion gene was not affected by salicylic acid (SA) alone, MeJA-inducible expression of the fusion gene was enhanced to about 2-fold by the presence of low concentrations of SA or aspirin. Thus, unlike MeJA-inducible gene impression in wounded leaves, JA-inducible expression of the ODC gene in tobacco BY-2 cells is not inhibited by SA. Analysis using serial deletions and internal deletions of the ODC gene promoter revealed that the sequence between -1457 and -1351 and the sequence between -943 and -746 are both important in the MeJA-inducible expression of the ODC promoter. These sequences did not contain several sequence motifs such as G-box that had been implicated to be involved in the MeJA-inducible expression of secondary-responsive genes in plants. Nuclear extracts prepared from tobacco BY-2 cells contained activities which specifically bind to the two regions of the ODC promoter important for the MeJA-responsible expression. Treatment of tobacco cells with MeJA did not affect the binding activities.
烟草BY-2细胞的鸟氨酸脱羧酶(ODC)基因的转录即使在蛋白质合成抑制剂存在的情况下也被激活。从烟草中分离到一个不含内含子的ODC核基因,由ODC启动子和GUS报告基因组成的融合基因(ODC: GUS)在转化的烟草BY-2细胞中对MeJA有较早的反应。虽然ODC: GUS融合基因的表达不受单独水杨酸(SA)的影响,但meja诱导的融合基因的表达在低浓度SA或阿司匹林的存在下增强了约2倍。因此,与meja诱导的基因在伤叶中的印象不同,ja诱导的ODC基因在烟草by -2细胞中的表达不受SA的抑制。对ODC基因启动子进行序列缺失和内部缺失分析,发现-1457 ~ -1351和-943 ~ -746在meja诱导的ODC启动子表达中都很重要。这些序列不包含一些序列基序,如G-box,这些序列基序与meja诱导的植物二级反应基因的表达有关。从烟草BY-2细胞中提取的核提取物含有特异性结合ODC启动子的两个区域的活性,这些区域对meja负责的表达很重要。MeJA对烟草细胞的结合活性没有影响。
项目成果
期刊论文数量(11)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Imanishi, S., Nakakita, M., Yamashita, K., Furuta, A., Utsuno, K., Muramoto, N., Kojima, H. and Nakamura, K.: "Aspirin and salicylic acid do not inhibit methyl jasmonate-inducible expression of a gene for ornithine decarboxylase in tobacco BY-2 cells"Bios
Imanishi, S.、Nakakita, M.、Yamashita, K.、Furuta, A.、Utsuno, K.、Muramoto, N.、Kojima, H. 和 Nakamura, K.:“阿司匹林和水杨酸不会抑制茉莉酸甲酯
- DOI:
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- 影响因子:0
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- 通讯作者:
Imanishi, S. 他4名: "An mRNA of tobacco cell, which is rapidly incible by methyl jasmonate in the presence of cycloheximide, codes for a putative glycosyltransferase"Plant Cell Physiol.. 39. 202-211 (1998)
Imanishi, S. 和其他 4 人:“在放线菌酮存在下,烟草细胞的 mRNA 会被茉莉酸甲酯快速裂解,编码推定的糖基转移酶”Plant Cell Physiol.. 39. 202-211 (1998)
- DOI:
- 发表时间:
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- 影响因子:0
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- 通讯作者:
S.Imanishi: "An mRNA of tobacco cell,which is rapidly inducible by methyl jasmonate in the presence of cycloheximide,codes for a putative glycosyltransferase." Plant Cell Physiol.39. 202-211 (1998)
S.Imanishi:“烟草细胞的 mRNA 在放线菌酮存在下可被茉莉酸甲酯快速诱导,编码一种假定的糖基转移酶。”
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- 发表时间:
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- 影响因子:0
- 作者:
- 通讯作者:
Imanishi, S. 他7名: "Aspirin and salicylic acid do not inhibit methyl jasmonate-inducible expression of a gene for ornithine decarboxylase in tobacco BY-2 cells"Biosci. Biotechnol. Biochem.. 64. 125-133 (2000)
Imanishi, S. 和其他 7 人:“阿司匹林和水杨酸不会抑制烟草 BY-2 细胞中茉莉酸甲酯诱导的鸟氨酸脱羧酶基因表达”Biosci. Biotechnol. 64. 125-133 (2000)
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- 发表时间:
- 期刊:
- 影响因子:0
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- 通讯作者:
S.Imanishi: "Jasmonate-induced accumulation of nicotine in tobacco cells occurs by non-coordinated induction of expression of genes for omithine decarboxylase and other enzymes." Plant Mol.Biol.38. 1101-1111 (1998)
S.Imanishi:“茉莉酸诱导的尼古丁在烟草细胞中的积累是通过不协调诱导鸟氨酸脱羧酶和其他酶的基因表达而发生的。”
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- 影响因子:0
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NAKAMURA Kenzo其他文献
NAKAMURA Kenzo的其他文献
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{{ truncateString('NAKAMURA Kenzo', 18)}}的其他基金
High-Throughput Genetic Identification of Regulatory Factors Involved in the Regulation of Seed Oil Storage Using Bioluminescence Automatic Monitoring System
利用生物发光自动监测系统对参与种子油储存调控的调控因子进行高通量遗传鉴定
- 批准号:
23380057 - 财政年份:2011
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$ 10.18万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Functional analysis of novel transcription factors of Arabidopsis thaliana involved in the regulation of nutrient storage.
拟南芥参与营养储存调节的新型转录因子的功能分析。
- 批准号:
18380065 - 财政年份:2006
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$ 10.18万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Study of Neutrino Mass and Mixing by Long Baseline Neutrino Oscillations : from K2K to a Next-Generation Experiment
通过长基线中微子振荡研究中微子质量和混合:从 K2K 到下一代实验
- 批准号:
15204023 - 财政年份:2003
- 资助金额:
$ 10.18万 - 项目类别:
Grant-in-Aid for Scientific Research (A)
New Developments of Accelerator Neutrino Experiments
加速器中微子实验新进展
- 批准号:
12440072 - 财政年份:2000
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$ 10.18万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Sugar-inducible gene expression and vacuolar accumulation of storage proteins
糖诱导基因表达和储存蛋白的液泡积累
- 批准号:
12138203 - 财政年份:2000
- 资助金额:
$ 10.18万 - 项目类别:
Grant-in-Aid for Scientific Research on Priority Areas
Flexible Organ Plan in Higher Plants
高等植物的灵活器官计划
- 批准号:
06278101 - 财政年份:1998
- 资助金额:
$ 10.18万 - 项目类别:
Grant-in-Aid for Scientific Research on Priority Areas
Analysis of Protein Transport to the Vacuole in Plants as a Basis for the Production of Usefull Proteins in Higher Plants
植物液泡蛋白质运输分析作为高等植物生产有用蛋白质的基础
- 批准号:
08660102 - 财政年份:1996
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$ 10.18万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
NU-UCB Cooperative Program on plant Molecular Biology
NU-UCB植物分子生物学合作项目
- 批准号:
07044189 - 财政年份:1995
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$ 10.18万 - 项目类别:
Grant-in-Aid for international Scientific Research
Genetic Program Controlling Metabolic Function of the Plant Organ
控制植物器官代谢功能的遗传程序
- 批准号:
06278102 - 财政年份:1994
- 资助金额:
$ 10.18万 - 项目类别:
Grant-in-Aid for Scientific Research on Priority Areas
Regulation of expression of genes coding for subunits of plant mitochondrial F1-ATPase
植物线粒体 F1-ATP 酶亚基编码基因表达的调控
- 批准号:
06660098 - 财政年份:1994
- 资助金额:
$ 10.18万 - 项目类别:
Grant-in-Aid for General Scientific Research (C)
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