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Small RNA sX13: A Multifaceted Regulator of Virulence in the Plant Pathogen Xanthomonas

机译:小RNA sX13:植物病原体黄单胞菌中毒力的多方面调节者。

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摘要

Small noncoding RNAs (sRNAs) are ubiquitous posttranscriptional regulators of gene expression. Using the model plant-pathogenic bacterium Xanthomonas campestris pv. vesicatoria (Xcv), we investigated the highly expressed and conserved sRNA sX13 in detail. Deletion of sX13 impinged on Xcv virulence and the expression of genes encoding components and substrates of the Hrp type III secretion (T3S) system. qRT-PCR analyses revealed that sX13 promotes mRNA accumulation of HrpX, a key regulator of the T3S system, whereas the mRNA level of the master regulator HrpG was unaffected. Complementation studies suggest that sX13 acts upstream of HrpG. Microarray analyses identified 63 sX13-regulated genes, which are involved in signal transduction, motility, transcriptional and posttranscriptional regulation and virulence. Structure analyses of in vitro transcribed sX13 revealed a structure with three stable stems and three apical C-rich loops. A computational search for putative regulatory motifs revealed that sX13-repressed mRNAs predominantly harbor G-rich motifs in proximity of translation start sites. Mutation of sX13 loops differentially affected Xcv virulence and the mRNA abundance of putative targets. Using a GFP-based reporter system, we demonstrated that sX13-mediated repression of protein synthesis requires both the C-rich motifs in sX13 and G-rich motifs in potential target mRNAs. Although the RNA-binding protein Hfq was dispensable for sX13 activity, the hfq mRNA and Hfq::GFP abundance were negatively regulated by sX13. In addition, we found that G-rich motifs in sX13-repressed mRNAs can serve as translational enhancers and are located at the ribosome-binding site in 5% of all protein-coding Xcv genes. Our study revealed that sX13 represents a novel class of virulence regulators and provides insights into sRNA-mediated modulation of adaptive processes in the plant pathogen Xanthomonas.
机译:小型非编码RNA(sRNA)是基因表达的普遍转录后调节因子。使用模型植物病原细菌Xanthomonas campestris pv。 vesicatoria(Xcv),我们详细研究了高表达和保​​守的sRNA sX13。 sX13的删除影响Xcv毒力和编码Hrp III型分泌(T3S)系统的成分和底物的基因的表达。 qRT-PCR分析表明,sX13促进HrpX的mRNA积累,HrpX是T3S系统的关键调控因子,而主调控因子HrpG的mRNA水平则不受影响。补充研究表明,sX13在HrpG的上游起作用。微阵列分析确定了63个sX13调控的基因,这些基因参与信号转导,运动性,转录和转录后调控以及毒力。体外转录的sX13的结构分析显示,该结构具有三个稳定的茎和三个顶部富含C的环。通过计算机搜索推定的调控基序,发现sX13抑制的mRNA在翻译起始位点附近主要带有富含G的基序。 sX13环的突变差异影响Xcv毒力和推定目标的mRNA丰度。使用基于GFP的报告系统,我们证明了sX13介导的蛋白合成阻遏既需要sX13中的富含C的基序,也需要潜在目标mRNA中的富含G的基序。尽管RNA结合蛋白Hfq对于sX13活性是必需的,但sX13负调控hfq mRNA和Hfq :: GFP的丰度。此外,我们发现sX13抑制的mRNA中富含G的基序可以充当翻译增强子,并且位于所有蛋白质编码Xcv基因的5%中的核糖体结合位点。我们的研究表明,sX13代表一类新型的毒力调节剂,并为植物病原体黄单胞菌中sRNA介导的适应性过程调节提供了见识。

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