Sensors of Environmental Stress

环境压力传感器

基本信息

项目摘要

Histidine kinase (Hik) and response regulator (Rre) constitute the twp-component system that is a signal perception/transduction pathway in prokaryotes and some eukaryotes. The cyanobacterium Synechocystis sp. PCC 6803, which performs oxygenic photosynthesis like plants, contains 47 genes for Hiks and 45 genes for Rres. We mutated these genes successfully, except three genes for Hiks and three genes for Rres, and constructed mutant libraries of Hiks and Rres. By screening the libraries by genome-wide expression of genes under various stress conditions with cDNA microarrays, we obtained the following results.Hyperosmotic stress, due to 0.5 M sorbitol, induced the expression of 246 genes. Screening of the above-mentioned mutant libraries with respect to the hyperosmotic stress-inducible expression of genes by the cDNA microarray method revealed that 60% of the hyperosmotic stress-inducible genes are under control of five two-component systems, namely, Hik33/Rre31, Hik16/Hik41/Rre17, Hik34/Rre1, Hik2/Rre1, and Hik10/Rre3. Remaining 40% of the hyperosmotic stress-inducible genes are under control of as-yet unidentified signal-transducing pathways.Salt stress, due to 0.5 M NaCl, induced the expression of 294 genes. Screening of the above-mentioned mutant libraries with respect to the salt stress-inducible expression of genes by the cDNA microarray method revealed that 70% of the salt stress-inducible genes are under control five two-component systems as in the case of hyperosmotic stress-inducible genes. However, genes under the individual Hik/Rre two-component systems are different between the salt stress and hyperosmotic stress. Remaining 30% of the salt stress-inducible genes are under control of as-yet unidentified signal-transducing pathways.
组氨酸激酶(Hik)和反应调节因子(Rre)组成了原核生物和某些真核生物的双组分信号转导系统。蓝细菌集胞藻PCC 6803,其像植物一样进行产氧光合作用,含有47个Hiks基因和45个Rres基因。除Hiks基因和Rres基因各3个外,其余基因均成功突变,并构建了Hiks和Rres突变体文库。通过用cDNA微阵列筛选在各种胁迫条件下全基因组表达基因的文库,我们获得了以下结果:高渗胁迫,由于0.5 M山梨醇,诱导246个基因的表达。通过cDNA微阵列方法筛选上述突变体文库中高渗胁迫诱导型基因表达,发现60%的高渗胁迫诱导型基因受5个双组分系统控制,即Hik 33/Rre 31、Hik 16/Hik 41/Rre 17、Hik 34/Rre 1、Hik 2/Rre 1和Hik 10/Rre 3。其余40%的高渗胁迫诱导基因的控制下,尚未确定的信号转导途径。盐胁迫,由于0.5 M NaCl,诱导294个基因的表达。通过cDNA微阵列方法筛选上述突变体文库中的盐胁迫诱导型基因表达,发现70%的盐胁迫诱导型基因与高渗胁迫诱导型基因的情况一样处于5个双组分系统的控制下。然而,在盐胁迫和高渗胁迫下,单个Hik/Rre双组分系统下的基因是不同的。其余30%的盐胁迫诱导基因的控制下,尚未确定的信号转导途径。

项目成果

期刊论文数量(124)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Sensors of abiotic stress in Synechocystis
  • DOI:
    10.1007/978-3-540-39402-0_5
  • 发表时间:
    2004
  • 期刊:
  • 影响因子:
    0
  • 作者:
    K. Mikami;I. Suzuki;N. Murata
  • 通讯作者:
    K. Mikami;I. Suzuki;N. Murata
K.Marin: "Identification of histidine kinases that act as sensors in the perception of salt stress in Synechocystis sp.PCC 6803."Proceedings of the National Academy of Science U S A.. 100. 9061-9066 (2003)
K.Marin:“集胞藻 PCC 6803 中作为盐胁迫感知传感器的组氨酸激酶的鉴定。”美国国家科学院院刊 100. 9061-9066 (2003)
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
  • 作者:
  • 通讯作者:
A.Ferjani: "Glucosylglycerol, a compatible solute, sustains cell division under salt stress."Plant Physiology. 131. 1628-1637 (2003)
A.Ferjani:“葡萄糖基甘油是一种相容性溶质,在盐胁迫下维持细胞分裂。”植物生理学。
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
  • 作者:
  • 通讯作者:
The SphS-SphR two component system is the exclusive sensor for the induction of gene expression in response to phosphate limitation in Synechocystis
  • DOI:
    10.1074/jbc.m313358200
  • 发表时间:
    2004-03-26
  • 期刊:
  • 影响因子:
    4.8
  • 作者:
    Suzuki, S;Ferjani, A;Murata, N
  • 通讯作者:
    Murata, N
Glucosylglycerol, a compatible solute, sustains cell division under salt stress
  • DOI:
    10.1104/pp.102.017277
  • 发表时间:
    2003-04-01
  • 期刊:
  • 影响因子:
    7.4
  • 作者:
    Ferjani, A;Mustardy, L;Murata, N
  • 通讯作者:
    Murata, N
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MURATA Norio其他文献

MURATA Norio的其他文献

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{{ truncateString('MURATA Norio', 18)}}的其他基金

Studies on low-temperature sensors and the mechanisms of acclimation to low-temperature
低温传感器及其低温适应机制研究
  • 批准号:
    13854002
  • 财政年份:
    2001
  • 资助金额:
    $ 41.66万
  • 项目类别:
    Grant-in-Aid for Scientific Research (S)
Stress Responses of Photosynthetic Organisms
光合生物的应激反应
  • 批准号:
    04273102
  • 财政年份:
    1996
  • 资助金额:
    $ 41.66万
  • 项目类别:
    Grant-in-Aid for Scientific Research on Priority Areas
Molecular mechanism of acclimation and tolerance to low temperature.
适应和耐受低温的分子机制。
  • 批准号:
    08102011
  • 财政年份:
    1996
  • 资助金额:
    $ 41.66万
  • 项目类别:
    Grant-in-Aid for Specially Promoted Research
Genetic engineering of temperature stress tolerance
温度胁迫耐受性基因工程
  • 批准号:
    06044233
  • 财政年份:
    1994
  • 资助金额:
    $ 41.66万
  • 项目类别:
    Grant-in-Aid for international Scientific Research
Molecular Mechanisms for Responses of Photosynthetic organisms to Environments
光合生物对环境响应的分子机制
  • 批准号:
    04273103
  • 财政年份:
    1992
  • 资助金额:
    $ 41.66万
  • 项目类别:
    Grant-in-Aid for Scientific Research on Priority Areas
植物の温度検知機構の分子生物学的解析
植物温度传感机制的分子生物学分析
  • 批准号:
    02404004
  • 财政年份:
    1990
  • 资助金额:
    $ 41.66万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (A)
耐冷性に関する形質転換植物の作製
与耐寒性相关的转化植物的创建
  • 批准号:
    01840027
  • 财政年份:
    1989
  • 资助金额:
    $ 41.66万
  • 项目类别:
    Grant-in-Aid for Developmental Scientific Research (B).
Studies on the Photochemical Reaction Center Complexes of Photosynthesis
光合作用光化学反应中心配合物的研究
  • 批准号:
    63044148
  • 财政年份:
    1988
  • 资助金额:
    $ 41.66万
  • 项目类别:
    Grant-in-Aid for international Scientific Research
Photosynthetic Genes and Their Expression
光合基因及其表达
  • 批准号:
    61304004
  • 财政年份:
    1986
  • 资助金额:
    $ 41.66万
  • 项目类别:
    Grant-in-Aid for Co-operative Research (A)

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