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Growth Phase and (p)ppGpp Control of IraD, a Regulator of RpoS Stability, in Escherichia coli▿

机译:大肠杆菌中RraS稳定性调节剂IraD的生长期和(p)ppGpp控制

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摘要

The antiadaptor protein IraD inhibits the proteolysis of the alternative sigma factor, RpoS, which promotes the synthesis of >100 genes during the general stress response and during stationary phase. Our previous results showed that IraD determines RpoS steady-state levels during exponential growth and mediates its stabilization after DNA damage. In this study, we show by promoter fusions that iraD was upregulated during the transition from exponential growth to stationary phase. The levels of RpoS likewise rose during this transition in a partially IraD-dependent manner. The expression of iraD was under the control of ppGpp. The expression of iraD required RelA and SpoT (p)ppGpp synthetase activities and was dramatically induced by a “stringent” allele of RNA polymerase, culminating in elevated levels of RpoS. Surprisingly, DksA, normally required for transcriptional effects of the stringent response, repressed iraD expression, suggesting that DksA can exert regulatory effects independent of and opposing those of (p)ppGpp. Northern blot analysis and 5′ rapid amplification of cDNA ends revealed two transcripts for iraD in wild-type strains; the smaller was regulated positively by RelA during growth; the larger transcript was induced specifically upon transition to stationary phase and was RelA SpoT dependent. A reporter fusion to the distal promoter indicated that it accounts for growth-phase regulation and DNA damage inducibility. DNA damage inducibility occurred in strains unable to synthesize (p)ppGpp, indicating an additional mode of regulation. Our results suggest that the induction of RpoS during transition to stationary phase and by (p)ppGpp occurs at least partially through IraD.
机译:抗调节蛋白IraD抑制了另类sigma因子RpoS的蛋白水解,该蛋白在一般应激反应期间和稳定期促进了> 100个基因的合成。我们以前的结果表明,IraD决定了指数增长过程中RpoS的稳态水平,并在DNA损伤后介导其稳定。在这项研究中,我们通过启动子融合显示iraD在从指数生长到稳定期的过渡过程中被上调。在此过渡过程中,RpoS的水平同样以部分依赖IraD的方式上升。 iraD的表达在ppGpp的控制下。 iraD的表达需要RelA和SpoT(p)ppGpp合成酶活性,并且被RNA聚合酶的“严格”等位基因极大地诱导,最终导致RpoS水平升高。出乎意料的是,严格应答的转录作用通常需要的DksA抑制了iraD表达,这表明DksA可以发挥独立于(p)ppGpp的调节作用并与之相反的调节作用。 Northern印迹分析和cDNA末端的5'快速扩增揭示了野生型菌株中iraD的两个转录本;较小的在生长过程中受到RelA的积极调节;较大的转录物在过渡到固定相时被特异性诱导,并且是RelA SpoT依赖性的。一个与远端启动子融合的报告基因表明,它负责生长阶段的调控和DNA损伤的诱导。 DNA损伤诱导性发生在无法合成(p)ppGpp的菌株中,这表明存在另一种调控模式。我们的结果表明,在过渡到固定相过程中和(p)ppGpp对RpoS的诱导至少部分通过IraD发生。

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