Landt Stephen G, Abeliuk Eduardo, McGrath Patrick T, Lesley Joseph A, McAdams Harley H, Shapiro Lucy
Department of Developmental Biology, School of Medicine, Stanford University, Stanford, CA 94305, USA.
Mol Microbiol. 2008 May;68(3):600-14. doi: 10.1111/j.1365-2958.2008.06172.x. Epub 2008 Mar 25.
Small non-coding RNAs (sRNAs) are active in many bacterial cell functions, including regulation of the cell's response to environmental challenges. We describe the identification of 27 novel Caulobacter crescentus sRNAs by analysis of RNA expression levels assayed using a tiled Caulobacter microarray and a protocol optimized for detection of sRNAs. The principal analysis method involved identification of sets of adjacent probes with unusually high correlation between the individual intergenic probes within the set, suggesting presence of a sRNA. Among the validated sRNAs, two are candidate transposase gene antisense RNAs. The expression of 10 of the sRNAs is regulated by either entry into stationary phase, carbon starvation, or rich versus minimal media. The expression of four of the novel sRNAs changes as the cell cycle progresses. One of these shares a promoter motif with several genes expressed at the swarmer-to-stalked cell transition; while another appears to be controlled by the CtrA global transcriptional regulator. The probe correlation analysis approach reported here is of general use for large-scale sRNA identification for any sequenced microbial genome.
小非编码RNA(sRNA)在许多细菌细胞功能中发挥作用,包括调节细胞对环境挑战的反应。我们通过分析使用平铺式新月柄杆菌微阵列和针对sRNA检测优化的方案测定的RNA表达水平,描述了27种新型新月柄杆菌sRNA的鉴定。主要分析方法包括鉴定一组相邻探针,该组内各个基因间探针之间具有异常高的相关性,这表明存在sRNA。在经过验证的sRNA中,有两种是候选转座酶基因反义RNA。其中10种sRNA的表达受进入稳定期、碳饥饿或丰富培养基与基本培养基的影响。随着细胞周期的进展,4种新型sRNA的表达发生变化。其中一种与在游动细胞到柄细胞转变时表达的几个基因共享一个启动子基序;而另一种似乎受全局转录调节因子CtrA控制。本文报道的探针相关性分析方法普遍适用于对任何已测序微生物基因组进行大规模sRNA鉴定。