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Transcriptional induction of an Agrobacterium regulatory gene at tandem promoters by plant-released phenolic compounds, phosphate starvation, and acidic growth media.植物释放的酚类化合物、磷饥饿和酸性生长培养基对农杆菌调控基因在串联启动子处的转录诱导作用。
J Bacteriol. 1990 May;172(5):2433-8. doi: 10.1128/jb.172.5.2433-2438.1990.
2
The regulatory VirG protein specifically binds to a cis-acting regulatory sequence involved in transcriptional activation of Agrobacterium tumefaciens virulence genes.调控蛋白VirG特异性结合参与根癌土壤杆菌毒力基因转录激活的顺式作用调控序列。
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3
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4
Controlled expression of the transcriptional activator gene virG in Agrobacterium tumefaciens by using the Escherichia coli lac promoter.通过使用大肠杆菌乳糖启动子来控制根癌土壤杆菌中转录激活基因virG的表达。
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本文引用的文献

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Virulence genes A, G, and D mediate the double-stranded border cleavage of T-DNA from the Agrobacterium Ti plasmid.毒力基因 A、G 和 D 介导农杆菌 Ti 质粒 T-DNA 的双链边界切割。
Proc Natl Acad Sci U S A. 1987 Apr;84(7):1881-5. doi: 10.1073/pnas.84.7.1881.
2
In vitro gene fusions that join an enzymatically active beta-galactosidase segment to amino-terminal fragments of exogenous proteins: Escherichia coli plasmid vectors for the detection and cloning of translational initiation signals.将具有酶活性的β-半乳糖苷酶片段与外源蛋白质的氨基末端片段连接的体外基因融合:用于检测和克隆翻译起始信号的大肠杆菌质粒载体。
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Design and development of amplifiable broad-host-range cloning vectors: analysis of the vir region of Agrobacterium tumefaciens plasmid pTiC58.可扩增的广宿主范围克隆载体的设计与开发:根癌土壤杆菌质粒pTiC58的vir区域分析
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Agrobacterium tumefaciens DNA and PS8 bacteriophage DNA not detected in crown gall tumors.在冠瘿瘤中未检测到根癌土壤杆菌DNA和PS8噬菌体DNA。
Proc Natl Acad Sci U S A. 1974 Sep;71(9):3672-6. doi: 10.1073/pnas.71.9.3672.
5
virA and virG control the plant-induced activation of the T-DNA transfer process of A. tumefaciens.virA和virG控制植物诱导的根癌土壤杆菌T-DNA转移过程的激活。
Cell. 1986 Aug 1;46(3):325-33. doi: 10.1016/0092-8674(86)90653-7.
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Characterization of the virA locus of Agrobacterium tumefaciens: a transcriptional regulator and host range determinant.根癌土壤杆菌virA基因座的特征:一种转录调节因子和宿主范围决定因素。
EMBO J. 1987 Apr;6(4):849-56. doi: 10.1002/j.1460-2075.1987.tb04830.x.
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Conserved domains in bacterial regulatory proteins that respond to environmental stimuli.对环境刺激作出反应的细菌调节蛋白中的保守结构域。
Cell. 1987 Jun 5;49(5):579-81. doi: 10.1016/0092-8674(87)90530-7.
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Differential induction of heat shock, SOS, and oxidation stress regulons and accumulation of nucleotides in Escherichia coli.大肠杆菌中热休克、SOS和氧化应激调节子的差异诱导及核苷酸积累
J Bacteriol. 1987 Jan;169(1):26-32. doi: 10.1128/jb.169.1.26-32.1987.
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Promoters of Agrobacterium tumefaciens Ti-plasmid virulence genes.根癌土壤杆菌Ti质粒毒力基因的启动子
Nucleic Acids Res. 1986 Feb 11;14(3):1355-64. doi: 10.1093/nar/14.3.1355.
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Rapid and efficient site-specific mutagenesis without phenotypic selection.无需表型选择的快速高效位点特异性诱变。
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植物释放的酚类化合物、磷饥饿和酸性生长培养基对农杆菌调控基因在串联启动子处的转录诱导作用。

Transcriptional induction of an Agrobacterium regulatory gene at tandem promoters by plant-released phenolic compounds, phosphate starvation, and acidic growth media.

作者信息

Winans S C

机构信息

Department of Microbiology, Cornell University, Ithaca, New York 14853-7201.

出版信息

J Bacteriol. 1990 May;172(5):2433-8. doi: 10.1128/jb.172.5.2433-2438.1990.

DOI:10.1128/jb.172.5.2433-2438.1990
PMID:2185220
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC208880/
Abstract

Transcription of the virG gene of Agrobacterium tumefaciens was previously shown to be expressed from two tandem promoters and to be responsive to three stimuli: plant-released phenolic compounds, phosphate starvation, and acidic media. In this report, I describe a set of deletions and other alterations of the 5' end of virG that show that the upstream promoter (P1) is necessary for induction by phenolic compounds and by phosphate starvation, whereas the downstream promoter (P2) is induced by acidic media. Upstream of promoter P1 there are three copies of a family of sequences (vir boxes) found near all VirA, VirG-inducible promoters. Site-directed mutagenesis of these sequences showed that vir box I and vir box III but not vir box II are needed for induction of P1 by acetosyringone. Induction of P1 by phosphate starvation requires vir box III (or an overlapping site), whereas vir box I and vir box II are not needed. The relative importance of promoters P1 and P2 in vir gene induction was tested by measuring the expression of a virB::lacZ fusion in strains containing mutations at either promoter P1 or P2. Mutations in either promoter significantly attenuated the expression of virB, indicating that both promoters play important roles in vir gene induction.

摘要

根癌土壤杆菌virG基因的转录先前已表明是由两个串联启动子表达,并对三种刺激有反应:植物释放的酚类化合物、磷饥饿和酸性培养基。在本报告中,我描述了一组virG 5'端的缺失和其他改变,结果表明上游启动子(P1)对于酚类化合物和磷饥饿诱导是必需的,而下游启动子(P2)由酸性培养基诱导。在启动子P1上游有一个序列家族(vir框)的三个拷贝,在所有VirA、VirG可诱导启动子附近都能找到。这些序列的定点诱变表明,vir框I和vir框III而非vir框II是乙酰丁香酮诱导P1所必需的。磷饥饿诱导P1需要vir框III(或一个重叠位点),而不需要vir框I和vir框II。通过测量在启动子P1或P2处含有突变的菌株中virB::lacZ融合蛋白的表达,测试了启动子P1和P2在vir基因诱导中的相对重要性。任一启动子中的突变都显著减弱了virB的表达,表明两个启动子在vir基因诱导中都起重要作用。