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大肠杆菌中硝酸盐对厌氧呼吸基因表达的调控

Nitrate regulation of anaerobic respiratory gene expression in Escherichia coli.

作者信息

Stewart V

机构信息

Section of Microbiology, Cornell University, Ithaca, New York 14853-8101.

出版信息

Mol Microbiol. 1993 Aug;9(3):425-34. doi: 10.1111/j.1365-2958.1993.tb01704.x.

Abstract

Synthesis of most anaerobic respiratory pathways is subject to dual regulation by anaerobiosis and nitrate. Anaerobic induction is mediated by the FNR protein. Dual interacting two-component regulatory systems mediate nitrate induction and repression. The response regulator protein NARL binds DNA to control nitrate induction and repression of genes encoding nitrate respiration enzymes and alternate anaerobic respiratory enzymes, respectively. The homologous protein NARP controls nitrite induction of at least two operons. Nitrate and nitrite signalling are both mediated by the homologous sensor proteins NARX and NARQ. Recent mutational analyses have defined a heptamer sequence necessary for specific DNA binding by the NARL protein. These heptamers are located at different positions in the control regions of different operons. The NARL protein-binding sites in the narG (nitrate reductase) and narK (nitrate-nitrite antiporter) operon control regions are located approximately 200bp upstream of the transcription initiation site. The integration host factor (IHF) greatly stimulates nitrate induction of these operons, indicating that a specific DNA loop brings NARL protein, bound at the upstream region, into the proximity of the promoter for transcription activation. Other NARL protein-dependent opersons do not require IHF for nitrate induction, and the arrangement of NARL heptamer sequences in these control regions is quite different. This complexity of signal transduction pathways, coupled with the diversity of control region architecture, combine to provide many interesting areas for future investigation. An additional challenge is to determine how or if the FNR and NARL proteins interact to mediate dual positive control of transcription initiation.

摘要

大多数厌氧呼吸途径的合成受到厌氧状态和硝酸盐的双重调控。厌氧诱导由FNR蛋白介导。双重相互作用的双组分调节系统介导硝酸盐诱导和抑制。响应调节蛋白NARL结合DNA,分别控制硝酸盐诱导和对编码硝酸盐呼吸酶及替代厌氧呼吸酶的基因的抑制。同源蛋白NARP控制至少两个操纵子的亚硝酸盐诱导。硝酸盐和亚硝酸盐信号传导均由同源传感蛋白NARX和NARQ介导。最近的突变分析确定了NARL蛋白特异性结合DNA所需的七聚体序列。这些七聚体位于不同操纵子控制区域的不同位置。narG(硝酸盐还原酶)和narK(硝酸盐 - 亚硝酸盐反向转运蛋白)操纵子控制区域中的NARL蛋白结合位点位于转录起始位点上游约200bp处。整合宿主因子(IHF)极大地刺激了这些操纵子的硝酸盐诱导,表明特定的DNA环将结合在上游区域的NARL蛋白带到启动子附近以激活转录。其他依赖NARL蛋白的操纵子在硝酸盐诱导时不需要IHF,并且这些控制区域中NARL七聚体序列的排列有很大不同。信号转导途径的这种复杂性,加上控制区域结构的多样性,共同为未来的研究提供了许多有趣的领域。另一个挑战是确定FNR和NARL蛋白如何相互作用或是否相互作用以介导转录起始的双重正调控。

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