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A variant of the Escherichia coli anaerobic transcription factor FNR exhibiting diminished promoter activation function enhances ionizing radiation resistance

机译:表现出启动子激活功能减弱的大肠杆菌厌氧转录因子FNR的变体增强了电离辐射的抵抗力

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摘要

We have previously generated four replicate populations of ionizing radiation (IR)-resistant Escherichia coli though directed evolution. Sequencing of isolates from these populations revealed that mutations affecting DNA repair (through DNA double-strand break repair and replication restart), ROS amelioration, and cell wall metabolism were prominent. Three mutations involved in DNA repair explained the IR resistance phenotype in one population, and similar DNA repair mutations were prominent in two others. The remaining population, IR-3-20, had no mutations in the key DNA repair proteins, suggesting that it had taken a different evolutionary path to IR resistance. Here, we present evidence that a variant of the anaerobic metabolism transcription factor FNR, unique to and isolated from population IR-3-20, plays a role in IR resistance. The F186I allele of FNR exhibits a diminished ability to activate transcription from FNR-activatable promoters, and furthermore reduces levels of intracellular ROS. The FNR F186I variant is apparently capable of enhancing resistance to IR under chronic irradiation conditions, but does not increase cell survival when exposed to acute irradiation. Our results underline the importance of dose rate on cell survival of IR exposure.
机译:通过定向进化,我们以前已经产生了四个抗电离辐射大肠埃希菌的重复种群。从这些种群分离株的测序表明,影响DNA修复(通过DNA双链断裂修复和复制重新开始),ROS改善和细胞壁代谢的突变非常突出。 DNA修复涉及的三个突变解释了一个群体的IR抗性表型,而其他两个群体中相似的DNA修复突变也很突出。其余的种群IR-3-20在关键的DNA修复蛋白中没有突变,这表明它对IR抗性采取了不同的进化途径。在这里,我们提供的证据表明,厌氧代谢转录因子FNR的变异体是IR-3-20群体中唯一的,并从中分离出来,在IR抗性中起作用。 FNR的F186I等位基因显示出从FNR可激活的启动子激活转录的能力减弱,并且进一步降低了细胞内ROS的水平。 FNR F186I变体显然能够增强在慢性照射条件下对IR的抵抗力,但在暴露于急性照射下不会增加细胞存活率。我们的结果强调了剂量率对IR暴露的细胞存活的重要性。

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