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Effects of H-NS and potassium glutamate on sigmaS- and sigma70-directed transcription in vitro from osmotically regulated P1 and P2 promoters of proU in Escherichia coli.H-NS和谷氨酸钾对大肠杆菌中渗透压调节的proU基因P1和P2启动子在体外由σS和σ70指导的转录的影响。
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2
In vivo expression from the RpoS-dependent P1 promoter of the osmotically regulated proU operon in Escherichia coli and Salmonella enterica serovar Typhimurium: activation by rho and hns mutations and by cold stress.大肠杆菌和鼠伤寒沙门氏菌中渗透压调节的proU操纵子的RpoS依赖性P1启动子的体内表达:rho和hns突变以及冷应激的激活作用
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本文引用的文献

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Regulatory characteristics and promoter analysis of csiE, a stationary phase-inducible gene under the control of sigma S and the cAMP-CRP complex in Escherichia coli.大肠杆菌中受σS和cAMP-CRP复合物调控的静止期诱导基因csiE的调控特性及启动子分析
Mol Microbiol. 1995 Oct;18(1):175-84. doi: 10.1111/j.1365-2958.1995.mmi_18010175.x.
2
Promoter selectivity of Escherichia coli RNA polymerase E sigma 70 and E sigma 38 holoenzymes. Effect of DNA supercoiling.大肠杆菌RNA聚合酶E σ70和E σ38全酶的启动子选择性。DNA超螺旋的影响。
J Biol Chem. 1996 Jan 26;271(4):1998-2004. doi: 10.1074/jbc.271.4.1998.
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Heterogeneity of the principal sigma factor in Escherichia coli: the rpoS gene product, sigma 38, is a second principal sigma factor of RNA polymerase in stationary-phase Escherichia coli.大肠杆菌中主要σ因子的异质性:rpoS基因产物σ38是静止期大肠杆菌中RNA聚合酶的第二个主要σ因子。
Proc Natl Acad Sci U S A. 1993 Apr 15;90(8):3511-5. doi: 10.1073/pnas.90.8.3511.
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The Escherichia coli nucleoid protein H-NS functions directly as a transcriptional repressor.大肠杆菌类核蛋白H-NS直接作为转录阻遏物发挥作用。
EMBO J. 1993 Mar;12(3):1039-46. doi: 10.1002/j.1460-2075.1993.tb05745.x.
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Osmotic regulation of rpoS-dependent genes in Escherichia coli.大肠杆菌中rpoS依赖性基因的渗透调节
J Bacteriol. 1993 Jan;175(1):259-65. doi: 10.1128/jb.175.1.259-265.1993.
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Sigma s-dependent promoters in Escherichia coli are located in DNA regions with intrinsic curvature.大肠杆菌中依赖σS的启动子位于具有固有曲率的DNA区域。
Nucleic Acids Res. 1993 Aug 11;21(16):3667-70. doi: 10.1093/nar/21.16.3667.
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The chromatin-associated protein H-NS alters DNA topology in vitro.与染色质相关的蛋白质H-NS在体外会改变DNA拓扑结构。
EMBO J. 1994 Jan 1;13(1):258-68. doi: 10.1002/j.1460-2075.1994.tb06256.x.
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Molecular characterization of the promoter of osmY, an rpoS-dependent gene.渗透压应激诱导基因osmY启动子的分子特征分析,该基因受rpoS调控
J Bacteriol. 1994 Jan;176(1):100-7. doi: 10.1128/jb.176.1.100-107.1994.
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In vitro functional characterization of overproduced Escherichia coli katF/rpoS gene product.过量表达的大肠杆菌katF/rpoS基因产物的体外功能特性分析
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10
The Escherichia coli proU promoter element and its contribution to osmotically signaled transcription activation.大肠杆菌脯氨酸摄取操纵子启动子元件及其对渗透信号转录激活的作用。
J Bacteriol. 1994 Jun;176(12):3638-45. doi: 10.1128/jb.176.12.3638-3645.1994.

H-NS和谷氨酸钾对大肠杆菌中渗透压调节的proU基因P1和P2启动子在体外由σS和σ70指导的转录的影响。

Effects of H-NS and potassium glutamate on sigmaS- and sigma70-directed transcription in vitro from osmotically regulated P1 and P2 promoters of proU in Escherichia coli.

作者信息

Rajkumari K, Kusano S, Ishihama A, Mizuno T, Gowrishankar J

机构信息

Centre for Cellular & Molecular Biology, Hyderabad, India.

出版信息

J Bacteriol. 1996 Jul;178(14):4176-81. doi: 10.1128/jb.178.14.4176-4181.1996.

DOI:10.1128/jb.178.14.4176-4181.1996
PMID:8763946
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC178175/
Abstract

We have used supercoiled DNA templates in this study to demonstrate that transcription in vitro from the P1 and P2 promoters of the osmoresponsive proU operon of Escherichia coli is preferentially mediated by the sigma(s) and sigma70-bearing RNA polymerase holoenzymes, respectively. Addition of potassium glutamate resulted in the activation of transcription from both P1 and P2 and also led to a pronounced enhancement of sigma(s) selectivity at the P1 promoter. Transcription from P2, and to a lesser extent from P1, was inhibited by the nucleoid protein H-NS but only in the absence of potassium glutamate. This study validates the existence of dual promoters with dual specificities for proU transcription. Our results also support the proposals that potassium, which is known to accumulate in cells grown at high osmolarity, is at least partially responsible for effecting the in vivo induction of proU transcription and that it does so through two mechanisms, directly by the activation of RNA polymerase and indirectly by the relief of repression imposed by H-NS.

摘要

在本研究中,我们使用了超螺旋DNA模板来证明,大肠杆菌渗透压响应性proU操纵子的P1和P2启动子的体外转录分别优先由含σS和σ70的RNA聚合酶全酶介导。添加谷氨酸钾导致P1和P2的转录激活,并且还导致P1启动子处σS选择性的显著增强。P2的转录以及程度较轻的P1的转录受到类核蛋白H-NS的抑制,但仅在没有谷氨酸钾的情况下。这项研究证实了proU转录具有双重特异性的双重启动子的存在。我们的结果还支持以下提议:已知在高渗透压下生长的细胞中积累的钾至少部分负责在体内诱导proU转录,并且它通过两种机制实现,直接通过激活RNA聚合酶,间接通过解除H-NS施加的抑制作用。