Department of Biology and Center for Life in Extreme Environments, Portland State University, Portland, OR 97201.
Microbiol Spectr. 2018 Apr;6(2). doi: 10.1128/microbiolspec.RWR-0004-2017.
Despite the central role of bacterial noncoding small RNAs (sRNAs) in posttranscriptional regulation, little is understood about their evolution. Here we compile what has been studied to date and trace a life cycle of sRNAs-from their mechanisms of emergence, through processes of change and frequent neofunctionalization, to their loss from bacterial lineages. Because they possess relatively unrestrictive structural requirements, we find that sRNA origins are varied, and include emergence as well as formation from preexisting genetic elements via duplication events and horizontal gene transfer. The need for only partial complementarity to their mRNA targets facilitates apparent rapid change, which also contributes to significant challenges in tracing sRNAs across broad evolutionary distances. We document that recently emerged sRNAs in particular evolve quickly, mirroring dynamics observed in microRNAs, their functional analogs in eukaryotes. Mutations in mRNA-binding regions, transcriptional regulator or sigma factor binding sites, and protein-binding regions are all likely sources of shifting regulatory roles of sRNAs. Finally, using examples from the few evolutionary studies available, we examine cases of sRNA loss and describe how these may be the result of adaptive in addition to neutral processes. We highlight the need for more-comprehensive analyses of sRNA evolutionary patterns as a means to improve novel sRNA detection, enhance genome annotation, and deepen our understanding of regulatory networks in bacteria.
尽管细菌非编码小 RNA(sRNA)在转录后调控中起着核心作用,但人们对它们的进化知之甚少。在这里,我们总结了迄今为止的研究成果,并追踪了 sRNA 的生命周期——从它们的出现机制,到变化过程和频繁的新功能化,再到它们从细菌谱系中的丢失。由于它们具有相对不受限制的结构要求,我们发现 sRNA 的起源多种多样,包括通过复制事件和水平基因转移从现有遗传元件中形成的出现。只需要与它们的 mRNA 靶标部分互补,就可以促进明显的快速变化,这也导致在跨越广泛进化距离追踪 sRNA 时面临重大挑战。我们记录到,特别是最近出现的 sRNA 进化得非常快,反映了真核生物中 miRNA 及其功能类似物的动态。mRNA 结合区域、转录调节因子或σ因子结合位点以及蛋白质结合区域的突变,都是 sRNA 调节作用转移的可能来源。最后,我们使用少数进化研究中的例子,检查了 sRNA 丢失的情况,并描述了这些丢失如何可能是适应过程的结果,而不仅仅是中性过程。我们强调需要更全面地分析 sRNA 的进化模式,以提高新型 sRNA 的检测、增强基因组注释,并加深我们对细菌中调控网络的理解。