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Evolutionary patterns of Escherichia coli small RNAs and their regulatory interactions

机译:大肠杆菌小RNA的进化模式及其调控相互作用

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摘要

Most bacterial small RNAs (sRNAs) are post-transcriptional regulators of gene expression, exerting their regulatory function by base-pairing with their target mRNAs. While it has become evident that sRNAs play central regulatory roles in the cell, little is known about their evolution and the evolution of their regulatory interactions. Here we used the prokaryotic phylogenetic tree to reconstruct the evolutionary history of Escherichia coli sRNAs and their binding sites on target mRNAs. We discovered that sRNAs currently present in E. coli mainly accumulated inside the Enterobacteriales order, succeeding the appearance of other types of noncoding RNAs and concurrently with the evolution of a variant of the Hfq protein exhibiting a longer C-terminal region. Our analysis of the evolutionary ages of sRNA–mRNA interactions revealed that while all sRNAs were evolutionarily older than most of their known binding sites on mRNA targets, for quite a few sRNAs there was at least one binding site that coappeared with or preceded them. It is conceivable that the establishment of these first interactions forced selective pressure on the sRNAs, after which additional targets were acquired by fitting a binding site to the active region of the sRNA. This conjecture is supported by the appearance of many binding sites on target mRNAs only after the sRNA gain, despite the prior presence of the target gene in ancestral genomes. Our results suggest a selective mechanism that maintained the sRNAs across the phylogenetic tree, and shed light on the evolution of E. coli post-transcriptional regulatory network.
机译:大多数细菌小RNA(sRNA)是基因表达的转录后调节剂,它们通过与靶标mRNA碱基配对发挥其调节功能。尽管很明显,sRNA在细胞中起着中心调控作用,但对其进化以及调控相互作用的进化知之甚少。在这里,我们使用原核系统树来重建大肠杆菌sRNA的进化历史及其在靶mRNA上的结合位点。我们发现,目前存在于大肠杆菌中的sRNA主要在肠杆菌内部积累,继而出现其他类型的非编码RNA,并与表现出更长C端区域的Hfq蛋白变体同时进化。我们对sRNA-mRNA相互作用的进化年龄的分析表明,尽管所有sRNA在进化上都比其在mRNA靶标上的大多数已知结合位点进化,但在相当多的sRNA上,至少有一个结合位点与之共存或先于它们。可以想象的是,这些第一相互作用的建立在sRNA上施加了选择性压力,此后,通过将结合位点适配到sRNA的活性区域获得了额外的靶标。尽管祖先基因组中先前存在靶基因,但只有在sRNA获得后,靶mRNA上才会出现许多结合位点,从而支持了这一推测。我们的结果提出了一种选择性机制,可在整个系统发育树中维持sRNA,并阐明大肠杆菌转录后调控网络的进化。

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