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1
New technologies to assess genotype-phenotype relationships.评估基因型与表型关系的新技术。
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2
The Escherichia coli BarA-UvrY two-component system is needed for efficient switching between glycolytic and gluconeogenic carbon sources.大肠杆菌的BarA-UvrY双组分系统是在糖酵解和糖异生碳源之间进行有效切换所必需的。
J Bacteriol. 2003 Feb;185(3):843-53. doi: 10.1128/JB.185.3.843-853.2003.
3
FlhD/FlhC is a regulator of anaerobic respiration and the Entner-Doudoroff pathway through induction of the methyl-accepting chemotaxis protein Aer.FlhD/FlhC是一种通过诱导甲基接受趋化蛋白Aer来调节无氧呼吸和Entner-Doudoroff途径的调节因子。
J Bacteriol. 2003 Jan;185(2):534-43. doi: 10.1128/JB.185.2.534-543.2003.
4
Regulation and mode of action of the second small RNA activator of RpoS translation, RprA.RpoS翻译的第二种小RNA激活剂RprA的调控及作用模式
Mol Microbiol. 2002 Nov;46(3):813-26. doi: 10.1046/j.1365-2958.2002.03203.x.
5
Transcriptome analysis of all two-component regulatory system mutants of Escherichia coli K-12.大肠杆菌K-12所有双组分调节系统突变体的转录组分析
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6
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Carbon and nitrogen substrate utilization by archival Salmonella typhimurium LT2 cells.鼠伤寒沙门氏菌LT2存档菌株细胞对碳源和氮源的利用情况
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Signal transduction and regulatory mechanisms involved in control of the sigma(S) (RpoS) subunit of RNA polymerase.参与RNA聚合酶σ(S)(RpoS)亚基调控的信号转导及调节机制。
Microbiol Mol Biol Rev. 2002 Sep;66(3):373-95, table of contents. doi: 10.1128/MMBR.66.3.373-395.2002.
9
Regulatory circuitry of the CsrA/CsrB and BarA/UvrY systems of Escherichia coli.大肠杆菌CsrA/CsrB和BarA/UvrY系统的调控电路
J Bacteriol. 2002 Sep;184(18):5130-40. doi: 10.1128/JB.184.18.5130-5140.2002.
10
The baeSR two-component regulatory system activates transcription of the yegMNOB (mdtABCD) transporter gene cluster in Escherichia coli and increases its resistance to novobiocin and deoxycholate.baeSR双组分调控系统激活大肠杆菌中yegMNOB(mdtABCD)转运蛋白基因簇的转录,并增强其对新生霉素和脱氧胆酸盐的抗性。
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对所有双组分系统缺失的大肠杆菌K-12突变体进行表型微阵列分析。

Phenotype microarray analysis of Escherichia coli K-12 mutants with deletions of all two-component systems.

作者信息

Zhou Lu, Lei Xiang-He, Bochner Barry R, Wanner Barry L

机构信息

Department of Biological Sciences, Purdue University, West Lafayette, Indiana 47907, USA.

出版信息

J Bacteriol. 2003 Aug;185(16):4956-72. doi: 10.1128/JB.185.16.4956-4972.2003.

DOI:10.1128/JB.185.16.4956-4972.2003
PMID:12897016
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC166450/
Abstract

Two-component systems are the most common mechanism of transmembrane signal transduction in bacteria. A typical system consists of a histidine kinase and a partner response regulator. The histidine kinase senses an environmental signal, which it transmits to its partner response regulator via a series of autophosphorylation, phosphotransfer, and dephosphorylation reactions. Much work has been done on particular systems, including several systems with regulatory roles in cellular physiology, communication, development, and, in the case of bacterial pathogens, the expression of genes important for virulence. We used two methods to investigate two-component regulatory systems in Escherichia coli K-12. First, we systematically constructed mutants with deletions of all two-component systems by using a now-standard technique of gene disruption (K. A. Datsenko and B. L. Wanner, Proc. Natl. Acad. Sci. USA 97:6640-6645, 2000). We then analyzed these deletion mutants with a new technology called Phenotype MicroArrays, which permits assays of nearly 2,000 growth phenotypes simultaneously. In this study we tested 100 mutants, including mutants with individual deletions of all two-component systems and several related genes, including creBC-regulated genes (cbrA and cbrBC), phoBR-regulated genes (phoA, phoH, phnCDEFGHIJKLMNOP, psiE, and ugpBAECQ), csgD, luxS, and rpoS. The results of this battery of nearly 200,000 tests provided a wealth of new information concerning many of these systems. Of 37 different two-component mutants, 22 showed altered phenotypes. Many phenotypes were expected, and several new phenotypes were also revealed. The results are discussed in terms of the biological roles and other information concerning these systems, including DNA microarray data for a large number of the same mutants. Other mutational effects are also discussed.

摘要

双组分系统是细菌中跨膜信号转导最常见的机制。一个典型的系统由一个组氨酸激酶和一个伴侣反应调节因子组成。组氨酸激酶感知环境信号,并通过一系列自磷酸化、磷酸转移和去磷酸化反应将其传递给其伴侣反应调节因子。针对特定系统已经开展了大量工作,包括在细胞生理学、通讯、发育中具有调节作用的几个系统,以及对于细菌病原体而言,在毒力方面重要基因的表达。我们使用两种方法来研究大肠杆菌K-12中的双组分调节系统。首先,我们利用一种现已成为标准的基因破坏技术(K. A. 达特森科和B. L. 万纳,《美国国家科学院院刊》97:6640 - 6645,2000年)系统地构建了所有双组分系统缺失的突变体。然后,我们使用一种名为表型微阵列的新技术分析这些缺失突变体,该技术允许同时检测近2000种生长表型。在本研究中,我们测试了100个突变体,包括所有双组分系统以及几个相关基因(包括creBC调节的基因[cbrA和cbrBC]、phoBR调节的基因[phoA、phoH、phnCDEFGHIJKLMNOP、psiE和ugpBAECQ]、csgD、luxS和rpoS)单个缺失的突变体。这一系列近200,000次测试的结果提供了关于许多这些系统的大量新信息。在37种不同的双组分突变体中,22种表现出改变的表型。许多表型是预期的,同时也揭示了几种新的表型。根据这些系统的生物学作用和其他信息(包括大量相同突变体的DNA微阵列数据)对结果进行了讨论。还讨论了其他突变效应。