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Regulation of Gene Expression by PrrA in Rhodobacter sphaeroides 2.4.1: Role of Polyamines and DNA Topology▿

机译:球形红细菌2.4.1中PrrA对基因表达的调节:多胺的作用和DNA拓扑▿

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摘要

In the present study, we show in vitro binding of PrrA, a global regulator in Rhodobacter sphaeroides 2.4.1, to the PrrA site 2, within the RSP3361 locus. Specific binding, as shown by competition experiments, requires the phosphorylation of PrrA. The binding affinity of PrrA for site 2 was found to increase 4- to 10-fold when spermidine was added to the binding reaction. The presence of extracellular concentrations of spermidine in growing cultures of R. sphaeroides gave rise to a twofold increase in the expression of the photosynthesis genes pucB and pufB, as well as the RSP3361 gene, under aerobic growth conditions, as shown by the use of lacZ transcriptional fusions, and led to the production of light-harvesting spectral complexes. In addition, we show that negative supercoiling positively regulates the expression of the RSP3361 gene, as well as pucB. We show the importance of supercoiling through an evaluation of the regulation of gene expression in situ by supercoiling, in the case of the former gene, as well as using the DNA gyrase inhibitor novobiocin. We propose that polyamines and DNA supercoiling act synergistically to regulate expression of the RSP3361 gene, partly by affecting the affinity of PrrA binding to the PrrA site 2 within the RSP3361 gene.
机译:在本研究中,我们显示了球形红球菌2.4.1中的全局调节剂PrrA与RSP3361基因座中PrrA位点2的体外结合。如竞争实验所示,特异性结合需要PrrA的磷酸化。当将亚精胺加入结合反应中时,发现PrrA对位点2的结合亲和力增加了4至10倍。如在lacZ的使用中所示,在需氧菌生长条件下,球形芽孢杆菌生长培养物中细胞外浓度亚精胺的存在使光合作用基因pucB和pufB以及RSP3361基因的表达增加了两倍。转录融合,并导致光捕获光谱复合物的产生。此外,我们显示负超螺旋正调节RSP3361基因以及pucB的表达。我们通过对超基因的原位基因表达调控的评估来显示超螺旋的重要性,在前一个基因的情况下,以及使用DNA促旋酶抑制剂新霉素。我们建议多胺和DNA超螺旋协同作用来调节RSP3361基因的表达,部分是通过影响PrrA与RSP3361基因内PrrA位点2的亲和力来实现的。

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