Raghavan Rahul, Kacharia Fenil R, Millar Jess A, Sislak Christine D, Ochman Howard
Department of Biology and Center for Life in Extreme Environments, Portland State University
Department of Biology and Center for Life in Extreme Environments, Portland State University.
Genome Biol Evol. 2015 Jan 18;7(2):557-66. doi: 10.1093/gbe/evv009.
Small RNAs (sRNAs) are short, transcribed regulatory elements that are typically encoded in the intergenic regions (IGRs) of bacterial genomes. Several sRNAs, first recognized in Escherichia coli, are conserved among enteric bacteria, but because of the regulatory roles of sRNAs, differences in sRNA repertoires might be responsible for features that differentiate closely related species. We scanned the E. coli MG1655 and Salmonella enterica Typhimurium genomes for nonsyntenic IGRs as a potential source of uncharacterized, species-specific sRNAs and found that genome rearrangements have reconfigured several IGRs causing the disruption and formation of sRNAs. Within an IGR that is present in E. coli but was disrupted in Salmonella by a translocation event is an sRNA that is associated with the FNR/CRP global regulators and influences E. coli biofilm formation. A Salmonella-specific sRNA evolved de novo through point mutations that generated a σ(70) promoter sequence in an IGR that arose through genome rearrangement events. The differences in the sRNA pools among bacterial species have previously been ascribed to duplication, deletion, or horizontal acquisition. Here, we show that genomic rearrangements also contribute to this process by either disrupting sRNA-containing IGRs or creating IGRs in which novel sRNAs may evolve.
小RNA(sRNA)是短的转录调控元件,通常编码在细菌基因组的基因间区域(IGR)中。最初在大肠杆菌中发现的几种sRNA在肠道细菌中是保守的,但由于sRNA的调控作用,sRNA库的差异可能是区分密切相关物种特征的原因。我们扫描了大肠杆菌MG1655和鼠伤寒沙门氏菌的基因组,寻找非同线IGR作为未表征的物种特异性sRNA的潜在来源,发现基因组重排重新配置了几个IGR,导致sRNA的破坏和形成。在大肠杆菌中存在但在沙门氏菌中因易位事件而被破坏的一个IGR内,有一种与FNR/CRP全局调节因子相关的sRNA,它影响大肠杆菌生物膜的形成。一种沙门氏菌特异性sRNA通过点突变从头进化而来,这些点突变在通过基因组重排事件产生的一个IGR中产生了一个σ(70)启动子序列。细菌物种间sRNA库的差异以前被归因于复制、缺失或水平获得。在这里,我们表明基因组重排也通过破坏含sRNA的IGR或创建可能进化出新sRNA的IGR来促进这一过程。