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对携带一个点突变的大肠杆菌半乳糖操纵子调控区进行的研究,该点突变同时使两个重叠启动子失活。与RNA聚合酶和环磷酸腺苷受体蛋白的相互作用。

Studies with the Escherichia coli galactose operon regulatory region carrying a point mutation that simultaneously inactivates the two overlapping promoters. Interactions with RNA polymerase and the cyclic AMP receptor protein.

作者信息

Ponnambalam S, Spassky A, Busby S

出版信息

FEBS Lett. 1987 Jul 13;219(1):189-96. doi: 10.1016/0014-5793(87)81214-0.

DOI:10.1016/0014-5793(87)81214-0
PMID:3297789
Abstract

We report in vitro studies of the interactions between purified E. coli RNA polymerase and DNA from the regulatory region of the E. coli galactose operon which carries a point mutation that simultaneously stops transcription initiation at the two normal start points, S1 and S2. In the presence of this point mutation, transcription initiates at a third start point 14/15 bp downstream of S1, showing that inactivation of the two normally active promoters, P1 and P2, unmasks a third weaker promoter, P3. Transcription initiation in the gal operon is normally regulated by the cyclic AMP receptor protein, CRP, that binds to the gal regulatory region and switches transcription from P2 to P1. With the point mutation, CRP binding switches transcription from P3 to P1, although the formation of transcriptionally competent complexes at P1 is very slow. The results are discussed with respect to the mechanism of transcription activation by the CRP factor and the similarities between the regulatory regions of the galactose and lactose operons.

摘要

我们报告了纯化的大肠杆菌RNA聚合酶与来自大肠杆菌半乳糖操纵子调控区的DNA之间相互作用的体外研究。该调控区带有一个点突变,该突变同时阻止了在两个正常起始点S1和S2处的转录起始。在存在这种点突变的情况下,转录在S1下游14/15 bp处的第三个起始点开始,这表明两个正常活跃的启动子P1和P2失活后,暴露出了第三个较弱的启动子P3。半乳糖操纵子中的转录起始通常受环腺苷酸受体蛋白CRP调控,CRP与半乳糖调控区结合并将转录从P2切换到P1。存在点突变时,CRP结合将转录从P3切换到P1,尽管在P1处形成具有转录活性的复合物非常缓慢。我们将结合CRP因子的转录激活机制以及半乳糖操纵子和乳糖操纵子调控区之间的相似性来讨论这些结果。

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1
Studies with the Escherichia coli galactose operon regulatory region carrying a point mutation that simultaneously inactivates the two overlapping promoters. Interactions with RNA polymerase and the cyclic AMP receptor protein.对携带一个点突变的大肠杆菌半乳糖操纵子调控区进行的研究,该点突变同时使两个重叠启动子失活。与RNA聚合酶和环磷酸腺苷受体蛋白的相互作用。
FEBS Lett. 1987 Jul 13;219(1):189-96. doi: 10.1016/0014-5793(87)81214-0.
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Two catabolite activator protein molecules bind to the galactose promoter region of Escherichia coli in the presence of RNA polymerase.在RNA聚合酶存在的情况下,两个分解代谢物激活蛋白分子结合到大肠杆菌的半乳糖启动子区域。
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Role of a second catabolite activator protein molecule in controlling initiation of transcription at the galactose operon of Escherichia coli.第二种分解代谢物激活蛋白分子在控制大肠杆菌半乳糖操纵子转录起始中的作用。
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Interactions of RNA polymerase and the cyclic AMP receptor protein on DNA of the E. coli galactose operon.RNA聚合酶与环腺苷酸受体蛋白在大肠杆菌半乳糖操纵子DNA上的相互作用。
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引用本文的文献

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2
Indirect read-out of the promoter DNA by RNA polymerase in the closed complex.RNA 聚合酶在封闭复合物中对启动子 DNA 的间接读取。
Nucleic Acids Res. 2013 Jan 7;41(1):366-77. doi: 10.1093/nar/gks1018. Epub 2012 Oct 31.
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A "master" in base unpairing during isomerization of a promoter upon RNA polymerase binding.RNA聚合酶结合时启动子异构化过程中碱基解配对的“主导者”。
Proc Natl Acad Sci U S A. 2001 Dec 18;98(26):14849-52. doi: 10.1073/pnas.261517398. Epub 2001 Dec 4.
4
Temperature-dependence of open-complex formation at two Escherichia coli promoters with extended -10 sequences.两个具有延伸 -10 序列的大肠杆菌启动子处开放复合物形成的温度依赖性
Biochem J. 1996 Jul 1;317 ( Pt 1)(Pt 1):305-11. doi: 10.1042/bj3170305.
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Structure of open promoter complexes with Escherichia coli RNA polymerase as revealed by the DNase I footprinting technique: compilation analysis.通过DNA酶I足迹技术揭示的大肠杆菌RNA聚合酶开放启动子复合物的结构:汇编分析
Nucleic Acids Res. 1995 Nov 25;23(22):4533-41. doi: 10.1093/nar/23.22.4533.
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E. coli RNA polymerase, deleted in the C-terminal part of its alpha-subunit, interacts differently with the cAMP-CRP complex at the lacP1 and at the galP1 promoter.在其α亚基的C末端部分缺失的大肠杆菌RNA聚合酶,在lacP1和galP1启动子处与cAMP-CRP复合物的相互作用不同。
Nucleic Acids Res. 1993 Jan 25;21(2):319-26. doi: 10.1093/nar/21.2.319.
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Interactions between the cyclic AMP receptor protein and the alpha subunit of RNA polymerase at the Escherichia coli galactose operon P1 promoter.环腺苷酸受体蛋白与大肠杆菌半乳糖操纵子P1启动子处RNA聚合酶α亚基之间的相互作用。
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Selectivity of the Escherichia coli RNA polymerase E sigma 38 for overlapping promoters and ability to support CRP activation.大肠杆菌RNA聚合酶E sigma 38对重叠启动子的选择性以及支持CRP激活的能力。
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Correlation between the conformation of Escherichia coli -10 hexamer sequences and promoter strength: use of orthophenanthroline cuprous complex as a structural index.大肠杆菌-10六聚体序列构象与启动子强度之间的相关性:使用邻菲罗啉亚铜配合物作为结构指标。
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