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Coordinated Hibernation of Transcriptional and Translational Apparatus during Growth Transition of Escherichia coli to Stationary Phase

机译:大肠杆菌向静止期生长过渡过程中转录和翻译设备的休眠冬眠

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摘要

In the process of Escherichia coli K-12 growth from exponential phase to stationary, marked alteration takes place in the pattern of overall genome expression through modulation of both parts of the transcriptional and translational apparatus. In transcription, the sigma subunit with promoter recognition properties is replaced from the growth-related factor RpoD by the stationary-phase-specific factor RpoS. The unused RpoD is stored by binding with the anti-sigma factor Rsd. In translation, the functional 70S ribosome is converted to inactive 100S dimers through binding with the ribosome modulation factor (RMF). Up to the present time, the regulatory mechanisms of expression of these two critical proteins, Rsd and RMF, have remained totally unsolved. In this study, attempts were made to identify the whole set of transcription factors involved in transcription regulation of the rsd and rmf genes using the newly developed promoter-specific transcription factor (PS-TF) screening system. In the first screening, 74 candidate TFs with binding activity to both of the rsd and rmf promoters were selected from a total of 194 purified TFs. After 6 cycles of screening, we selected 5 stress response TFs, ArcA, McbR, RcdA, SdiA, and SlyA, for detailed analysis in vitro and in vivo of their regulatory roles. Results indicated that both rsd and rmf promoters are repressed by ArcA and activated by McbR, RcdA, SdiA, and SlyA. We propose the involvement of a number of TFs in simultaneous and coordinated regulation of the transcriptional and translational apparatus. By using genomic SELEX (gSELEX) screening, each of the five TFs was found to regulate not only the rsd and rmf genes but also a variety of genes for growth and survival. IMPORTANCE During the growth transition of E. coli from exponential phase to stationary, the genome expression pattern is altered markedly. For this alteration, the transcription apparatus is altered by binding of anti-sigma factor Rsd to the RpoD sigma factor for sigma factor replacement, while the translation machinery is modulated by binding of RMF to 70S ribosome to form inactive ribosome dimer. Using the PS-TF screening system, a number of TFs were found to bind to both the rsd and rmf promoters, of which the regulatory roles of 5 representative TFs (one repressor ArcA and the four activators McbR, RcdA, SdiA, and SlyA) were analyzed in detail. The results altogether indicated the involvement of a common set of TFs, each sensing a specific environmental condition, in coordinated hibernation of the transcriptional and translational apparatus for adaptation and survival under stress conditions.
机译:在大肠杆菌K-12从指数期到静止期生长的过程中,通过调节转录和翻译装置的两个部分,整个基因组表达模式发生了明显的变化。在转录中,具有启动子识别特性的sigma亚基由固定相特异性因子RpoS代替了生长相关因子RpoD。通过与反西格玛因子Rsd绑定来存储未使用的RpoD。在翻译中,功能性70S核糖体通过与核糖体调节因子(RMF)结合而转化为非活性的100S二聚体。到目前为止,这两种关键蛋白Rsd和RMF的表达调控机制仍未完全解决。在这项研究中,尝试使用新开发的启动子特异性转录因子(PS-TF)筛选系统来鉴定涉及rsd和rmf基因转录调控的整套转录因子。在第一次筛选中,从总共194个纯化的TF中选择了对rsd和rmf启动子都具有结合活性的74个候选TF。经过6个筛选周期,我们选择了5个应激反应TF,ArcA,McbR,RcdA,SdiA和SlyA,以在体内和体外详细分析其调节作用。结果表明,rsd和rmf启动子都被ArcA抑制,并被McbR,RcdA,SdiA和SlyA激活。我们建议在转录和翻译装置的同步和协调调控中涉及许多TF。通过使用基因组SELEX(gSELEX)筛选,发现五个TF中的每一个不仅调节rsd和rmf基因,而且还调节各种基因的生长和存活。重要说明在大肠杆菌从指数期到静止期的生长过渡过程中,基因组表达模式发生了明显变化。对于这种改变,通过将抗-σ因子Rsd与RpoD-σ因子结合以改变σ因子来改变转录装置,同时通过将RMF与70S核糖体结合形成无活性的核糖体二聚体来调节翻译机制。使用PS-TF筛选系统,发现许多TF与rsd和rmf启动子结合,其中5个代表性TF(一个阻遏物ArcA和四个激活剂McbR,RcdA,SdiA和SlyA)具有调节作用。进行了详细分析。结果完全表明,一组共同的TF参与了转录和翻译装置的冬眠,以适应压力条件下的适应和生存,每个TF都感知特定的环境条件。

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