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大肠杆菌对外部铜的转录反应。

Transcriptional response of Escherichia coli to external copper.

作者信息

Yamamoto Kaneyoshi, Ishihama Akira

机构信息

Department of Agricultural Chemistry, Kinki University, Nakamachi 3327-204, Nara 631-8505, Japan.

出版信息

Mol Microbiol. 2005 Apr;56(1):215-27. doi: 10.1111/j.1365-2958.2005.04532.x.

Abstract

Transcriptional response of Escherichia coli upon exposure to external copper was studied using DNA microarray and in vivo and in vitro transcription assays. Transcription of three hitherto-identified copper-responsive genes, copA (copper efflux transporter), cueO (multicopper oxidase) and cusC (tripartite copper pump component) became maximum at 5 min after addition of copper sulphate, and thereafter decreased to the preshift levels within 30 min. Microarray analysis at 5 min after addition of copper indicated that a total of at least 29 genes including these three known genes were markedly and specifically affected (28 upregulated and one downregulated). Transcription of the divergent operons, cusCFB and cusRS, was found to be activated by CusR, which bound to a CusR box between the cusC and cusR promoters. Except for this site, the CusR box was not identified in the entire E. coli genome. On the other hand, transcription of copA and cueO was found to be activated by another copper-responsive factor CueR, which bound to a conserved inverted repeat sequence, CueR box. A total of 197 CueR boxes were identified on the E. coli genome, including the CueR box associated with the moa operon for molybdenum cofactor synthesis. At least 10 copper-induced genes were found to be under the control of CpxAR two-component system, indicating that copper is one of the signals for activation of the CpxAR system. In addition, transcription of yedWV, a putative two-component system, was activated by copper in CusR-dependent manner. Taken together we conclude that the copper-responsive genes are organized into a hierarchy of the regulation network, forming at least four regulons, i.e. CueR, CusR, CpxR and YedW regulons. These copper-responsive regulons appear to sense and respond to different concentrations of external copper.

摘要

利用DNA微阵列以及体内和体外转录试验,研究了大肠杆菌暴露于外部铜时的转录反应。三个迄今已鉴定的铜响应基因copA(铜外排转运蛋白)、cueO(多铜氧化酶)和cusC(三方铜泵组件)的转录在添加硫酸铜后5分钟达到最大值,此后在30分钟内降至预转变水平。添加铜后5分钟的微阵列分析表明,包括这三个已知基因在内,共有至少29个基因受到显著且特异性的影响(28个上调,1个下调)。发现分歧操纵子cusCFB和cusRS的转录由CusR激活,CusR与cusC和cusR启动子之间的一个CusR框结合。除了这个位点外,在整个大肠杆菌基因组中未鉴定到CusR框。另一方面,发现copA和cueO的转录由另一种铜响应因子CueR激活,CueR与一个保守的反向重复序列CueR框结合。在大肠杆菌基因组上共鉴定到197个CueR框,包括与钼辅因子合成的moa操纵子相关的CueR框。发现至少10个铜诱导基因受CpxAR双组分系统的控制,表明铜是激活CpxAR系统的信号之一。此外,推定的双组分系统yedWV的转录以依赖CusR的方式被铜激活。综上所述,我们得出结论,铜响应基因被组织成一个调控网络层次结构,形成至少四个调控子,即CueR、CusR、CpxR和YedW调控子。这些铜响应调控子似乎能感知并响应不同浓度的外部铜。

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