National Laboratory for Scientific Computing (LNCC), Petrópolis, RJ, Brazil.
Laboratory of Microbiology, Institute of Biology, Federal University of Rio de Janeiro (UFRJ), Rio de Janeiro, RJ, CEP 21941-590, Brazil.
Microbiology (Reading). 2010 Aug;156(Pt 8):2452-2458. doi: 10.1099/mic.0.039149-0. Epub 2010 May 6.
The discovery of non-coding RNA (ncRNA) has been mainly limited to laboratory model systems and human pathogenic bacteria. In this study, we begin to explore the ncRNA diversity in four recently sequenced environmental Vibrio species (Vibrio alginolyticus 40B, Vibrio communis 1DA3, Vibrio mimicus VM573 and Vibrio campbellii BAA-1116) by performing in silico searches using Infernal and Rfam for the identification of putative ncRNA-encoding genes. This search method resulted in the identification of 31-38 putative ncRNA genes per species and the total ncRNA catalogue spanned an assortment of regulatory mechanisms (riboswitches, cis-encoded ncRNAs, trans-encoded ncRNAs, modulators of protein activity, ribonucleoproteins, transcription termination ncRNAs and unknown). We chose to experimentally validate the identifications for V. campbellii BAA-1116 using a microarray-based expression profiling strategy. Transcript hybridization to tiled probes targeting annotated V. campbellii BAA-1116 intergenic regions revealed that 21 of the 38 predicted ncRNA genes were expressed in mid-exponential-phase cultures grown in nutrient-rich medium. The microarray findings were confirmed by testing a subset of three highly expressed (6S, tmRNA and TPP-2) and three moderately expressed (CsrB, GcvB and purine) ncRNAs via reverse transcription PCR. Our findings provide new information on the diversity of ncRNA in environmental vibrios while simultaneously promoting a more accurate annotation of genomic intergenic regions.
非编码 RNA (ncRNA) 的发现主要局限于实验室模型系统和人类致病菌。在这项研究中,我们开始通过使用 Infernal 和 Rfam 进行计算机搜索,来探索最近测序的四种环境弧菌(Alginate-degrading bacterium 40B、Commensal bacterium 1DA3、Mimic bacterium VM573 和Campbellii bacterium BAA-1116)中的 ncRNA 多样性,以鉴定可能的 ncRNA 编码基因。这种搜索方法鉴定出每个物种的 31-38 个可能的 ncRNA 基因,总 ncRNA 目录涵盖了一系列调节机制(核糖开关、顺式编码 ncRNA、反式编码 ncRNA、蛋白质活性调节剂、核糖核蛋白、转录终止 ncRNA 和未知)。我们选择使用基于微阵列的表达谱分析策略来实验验证 Campbellii bacterium BAA-1116 的鉴定。针对注释的Campbellii bacterium BAA-1116 基因间区的靶向探针的转录杂交显示,在营养丰富的培养基中生长的指数中期培养物中表达了 38 个预测 ncRNA 基因中的 21 个。通过测试三个高度表达(6S、tmRNA 和 TPP-2)和三个中度表达(CsrB、GcvB 和嘌呤)ncRNA 的子集,通过逆转录 PCR 验证了微阵列的发现。我们的发现提供了有关环境弧菌中 ncRNA 多样性的新信息,同时促进了基因组基因间区的更准确注释。