Amin Shivam V, Roberts Justin T, Patterson Dillon G, Coley Alexander B, Allred Jonathan A, Denner Jason M, Johnson Justin P, Mullen Genevieve E, O'Neal Trenton K, Smith Jason T, Cardin Sara E, Carr Hank T, Carr Stacie L, Cowart Holly E, DaCosta David H, Herring Brendon R, King Valeria M, Polska Caroline J, Ward Erin E, Wise Alice A, McAllister Kathleen N, Chevalier David, Spector Michael P, Borchert Glen M
a Department of Biology , University of South Alabama , Mobile , AL.
b Department of Biomedical Sciences , University of South Alabama , Mobile , AL.
RNA Biol. 2016;13(3):331-42. doi: 10.1080/15476286.2016.1144010. Epub 2016 Feb 6.
Small RNAs (sRNAs) are short (∼50-200 nucleotides) noncoding RNAs that regulate cellular activities across bacteria. Salmonella enterica starved of a carbon-energy (C) source experience a host of genetic and physiological changes broadly referred to as the starvation-stress response (SSR). In an attempt to identify novel sRNAs contributing to SSR control, we grew log-phase, 5-h C-starved and 24-h C-starved cultures of the virulent Salmonella enterica subspecies enterica serovar Typhimurium strain SL1344 and comprehensively sequenced their small RNA transcriptomes. Strikingly, after employing a novel strategy for sRNA discovery based on identifying dynamic transcripts arising from "gene-empty" regions, we identify 58 wholly undescribed Salmonella sRNA genes potentially regulating SSR averaging an ∼1,000-fold change in expression between log-phase and C-starved cells. Importantly, the expressions of individual sRNA loci were confirmed by both comprehensive transcriptome analyses and northern blotting of select candidates. Of note, we find 43 candidate sRNAs share significant sequence identity to characterized sRNAs in other bacteria, and ∼70% of our sRNAs likely assume characteristic sRNA structural conformations. In addition, we find 53 of our 58 candidate sRNAs either overlap neighboring mRNA loci or share significant sequence complementarity to mRNAs transcribed elsewhere in the SL1344 genome strongly suggesting they regulate the expression of transcripts via antisense base-pairing. Finally, in addition to this work resulting in the identification of 58 entirely novel Salmonella enterica genes likely participating in the SSR, we also find evidence suggesting that sRNAs are significantly more prevalent than currently appreciated and that Salmonella sRNAs may actually number in the thousands.
小RNA(sRNA)是短的(约50 - 200个核苷酸)非编码RNA,可调节细菌中的细胞活动。缺乏碳源能量(C)的肠炎沙门氏菌会经历一系列广泛称为饥饿应激反应(SSR)的遗传和生理变化。为了鉴定有助于SSR调控的新型sRNA,我们培养了强毒肠炎沙门氏菌亚种肠炎血清型鼠伤寒菌株SL1344的对数期、5小时碳饥饿和24小时碳饥饿培养物,并对其小RNA转录组进行了全面测序。引人注目的是,在采用一种基于识别来自“基因空”区域的动态转录本的新型sRNA发现策略后,我们鉴定出58个完全未描述的沙门氏菌sRNA基因,它们可能调节SSR,在对数期和碳饥饿细胞之间的表达平均变化约1000倍。重要的是,通过全面的转录组分析和对选定候选物的Northern印迹法证实了单个sRNA位点的表达。值得注意的是,我们发现43个候选sRNA与其他细菌中已鉴定的sRNA具有显著的序列同一性,并且我们的sRNA中约70%可能具有特征性的sRNA结构构象。此外,我们发现58个候选sRNA中有53个要么与相邻的mRNA位点重叠,要么与SL1344基因组中其他地方转录的mRNA具有显著的序列互补性,这强烈表明它们通过反义碱基配对调节转录本的表达。最后,除了这项工作导致鉴定出58个可能参与SSR的全新肠炎沙门氏菌基因外,我们还发现有证据表明sRNA比目前所认识的更为普遍,并且沙门氏菌sRNA实际上可能数以千计。