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首页> 外文期刊>The ISME journal emultidisciplinary journal of microbial ecology >A framework for the computational prediction and analysis of non-coding RNAs in microbial environmental populations and their experimental validation
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A framework for the computational prediction and analysis of non-coding RNAs in microbial environmental populations and their experimental validation

机译:微生物环境群体中非编码RNA的计算预测和分析的框架及其实验验证

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摘要

Small regulatory RNAs and antisense RNAs play important roles in the regulation of gene expression in bacteria but are underexplored, especially in natural populations. While environmentally relevant microbes often are not amenable to genetic manipulation or cannot be cultivated in the laboratory, extensive metagenomic and metatranscriptomic datasets for these organisms might be available. Hence, dedicated workflows for specific analyses are needed to fully benefit from this information. Here, we identified abundant sRNAs from oceanic environmental populations of the ecologically important primary producer Prochlorococcus starting from a metatranscriptomic differential RNA-Seq (mdRNA-Seq) dataset. We tracked their homologs in laboratory isolates, and we provide a framework for their further detailed characterization. Several of the experimentally validated sRNAs responded to ecologically relevant changes in cultivation conditions. The expression of the here newly discovered sRNA Yfr28 was highly stimulated in low-nitrogen conditions. Its predicted top targets include mRNAs encoding cell division proteins, a sigma factor, and several enzymes and transporters, suggesting a pivotal role of Yfr28 in the coordination of primary metabolism and cell division. A cis-encoded antisense RNA was identified as a possible positive regulator of atpF encoding subunit b' of the ATP synthase complex. The presented workflow will also be useful for other environmentally relevant microorganisms for which experimental validation abilities are frequently limiting although there is wealth of sequence information available.
机译:小型监管RNA和反义RNA在细菌中基因表达的调节中起重要作用,但望而轻松,特别是在天然群体中。虽然环境相关的微生物通常不适合遗传操作,但不能在实验室中培养,这些生物体的广泛的偏见和MetaTransfradomic数据集可以获得。因此,需要为特定分析进行专用工作流,以完全受益于此信息。在这里,我们从MetaTranscriptomic差异RNA-SEQ(MDRNA-SEQ)数据集开始,从生态上重要的主要生产者促核癌的海洋环境群体中鉴定了丰富的SRNA。我们在实验室孤立中追踪他们的同源物,我们提供了一个框架,以便进一步详细表征。一些实验验证的SRNA响应了培养条件的生态相关变化。这里的表达新发现的SRNA YFR28在低氮气条件下高度刺激。其预测的顶部靶标包括编码细胞分裂蛋白,Σ因素和几种酶和转运蛋白的MRNA,表明YFR28在初级代谢和细胞分裂协调中的关键作用。将CIS编码的反义RNA鉴定为ATP合酶络合物的ATPF编码亚基B'的可能阳性调节剂。虽然有丰富的序列信息,所呈现的工作流程对其他环境相关的微生物频繁限制也很有用。

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