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Evolutionary patterns of Escherichia coli small RNAs and their regulatory interactions

机译:大肠杆菌小RNA的进化模式及其监管互动

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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)是基因表达后的转录稳态因子,通过与其靶MRNA的碱基配对施加调节功能。虽然已经变得显然,SRNA在细胞中发挥中央监管角色,但对他们的演变而众所周知,其调节互动的演变。在这里,我们使用了原核系统发育树来重建靶MRNA上的大肠杆菌SRNA的进化历史及其结合位点。我们发现目前存在于大肠杆菌中的SRNA主要累积在进肠杆菌的顺序内,并且随着具有较长C末端区域的HFQ蛋白的变体的演变成功地形成了其他类型的非沉积RNA的外观。我们对SRNA-mRNA相互作用的进化衰老的分析表明,虽然所有SRNA在mRNA靶标中的大部分已知的结合位点较大,但是对于相当多的SRNA,存在至少一个薄膜涂覆或前面的结合位点。可以想到,在SRNA上建立这些第一相互作用强制选择性压力,之后通过将结合位点装配到SRNA的有源区来获得另外的靶标。尽管祖先基因组中的靶基因的存在,但在SRNA增益之后,才能在靶mRNA上的许多结合位点的出现来支持该猜测。我们的研究结果表明,一种选择性机制,将跨系统发育树上的SRNA保持,并在转录后转录后调节网络的演变上脱光。

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