首页> 外文会议>2010 International Conference on Bioinformatics and Biomedical Technology (ICBBT 2010) >Computational prediction of small non-coding RNA within distal 3'region of 16SrRNA gene of Bacillus sp. strain SJ-101
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Computational prediction of small non-coding RNA within distal 3'region of 16SrRNA gene of Bacillus sp. strain SJ-101

机译:小芽孢杆菌16SrRNA基因远端3'区域内的小非编码RNA的计算预测。菌株SJ-101

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Computational ribonucleomics of heavy metal stress tolerant Bacillus sp. strain SJ-101 16SrRNA gene has led to the identification of a novel small non-coding RNA (sRNA) and promoter-like sequences within 3'' region of the gene. Using RNAz web server, a 123 bp long functional sRNA with significant thermodynamic stability (Energy contribution: −25.2) and evolutionary conservation (structure conservation index: 0.63) with a SVM RNA class probability (p) of 0.98 was predicted. The clustal W alignment revealed ∼79 % sequence homology with OxySRNA of Salmonella spp. in sRNAMap database. The Hfq binding site mapped within sRNA showed high sequence similarity with the Hfq elements in OxySRNA family. The target sites for SJ-101 sRNA were identified as ywqE, glpD, yomN and ywjE genes of Bacillus subtilis employing TargetRNA tool. Furthermore, using BPROM software, the regulatory motifs like −35 and −10 boxes were mapped at 1166 and 1187 positions, respectively. The cis-acting elements as the binding sites for transcription factors (TF) were identified at positions 1184 and 1188 within the same region. Thus, it is concluded that sRNAs are widely distributed and that these functional elements are implicated in fine tuning of gene regulatory processes under stress conditions.
机译:重金属胁迫耐受芽孢杆菌的计算核糖核酸。菌株SJ-101 16SrRNA基因已导致鉴定了该基因3英寸区域内的新型小非编码RNA(sRNA)和启动子样序列。使用RNAz Web服务器,预测了123 bp长的功能性sRNA,具有显着的热力学稳定性(能量贡献:-25.2)和进化保守性(结构保守性指数:0.63),SVM RNA类概率(p)为0.98。簇状W比对表明与沙门氏菌的OxySRNA具有约79%的序列同源性。在sRNAMap数据库中。映射到sRNA中的Hfq结合位点显示与OxySRNA家族中的Hfq元件高度相似。 SJ-101 sRNA的靶位点使用TargetRNA工具鉴定为枯草芽孢杆菌的ywqE,glpD,yomN和ywjE基因。此外,使用BPROM软件,将-35和-10框等调控基元分别定位在1166和1187位置。在相同区域内的位置1184和1188处确定了作为转录因子(TF)结合位点的顺式作用元件。因此,得出的结论是,sRNA广泛分布,并且这些功能元件与应激条件下基因调控过程的微调有关。

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