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Conservation of the binding site for the arginine repressor in all bacterial lineages

机译:保留所有细菌谱系中精氨酸阻遏物的结合位点

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摘要

Background:The arginine repressor ArgR/AhrC is a transcription factor universally conserved in bacterial genomes. Its recognition signal (the ARG box), a weak palindrome, is also conserved between genomes, despite a very low degree of similarity between individual sites within a genome. Thus, the arginine repressor is different from two other universal transcription factors - HrcA, whose recognition signal is very strongly conserved both within and between genomes, and LexA/DinR, whose signal is strongly conserved within, but not between, genomes. The arginine regulon is well studied in Escherichia coli and to some extent in Bacillus subtilis and some other genomes. Here, we apply the comparative genomic approach to the prediction of the ArgR-binding sites in all completely sequenced bacterial genomes.
机译:背景:精氨酸阻遏物ArgR / AhrC是细菌基因组中普遍保守的转录因子。尽管基因组中单个位点之间的相似度非常低,但它的识别信号(ARG盒)(一种弱回文)在基因组之间也很保守。因此,精氨酸阻遏物不同于另外两个通用转录因子-HrcA和LexA / DinR,后者的识别信号在基因组之内和之间都非常保守,而hrA的识别信号在基因组之内和之间都非常保守。精氨酸调节子在大肠杆菌中以及在一定程度上在枯草芽孢杆菌和一些其他基因组中得到了很好的研究。在这里,我们将比较基因组方法应用于所有完全测序的细菌基因组中ArgR结合位点的预测。

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