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Hfq 和 sRNA179 抑制铜绿假单胞菌 cAMP-Vfr 和 III 型分泌调节子的表达。

Hfq and sRNA 179 Inhibit Expression of the Pseudomonas aeruginosa cAMP-Vfr and Type III Secretion Regulons.

机构信息

Department of Microbiology and Immunology, University of Iowa, Iowa City, Iowa, USA.

Department of Medicine, Yale University School of Medicine, New Haven, Connecticut, USA.

出版信息

mBio. 2020 Jun 16;11(3):e00363-20. doi: 10.1128/mBio.00363-20.

Abstract

is a Gram-negative opportunistic pathogen causing skin and soft tissue, respiratory, and bloodstream infections. The type III secretion system (T3SS) is one important virulence factor. Production of the T3SS is controlled by ExsA, a transcription factor that activates expression of the entire T3SS regulon. Global regulators including Vfr, RsmA, and Hfq also contribute to regulation of the T3SS. Vfr is a cAMP-responsive transcription factor that activates transcription. RsmA, an RNA-binding protein, inversely controls expression of the T3SS and the type VI secretion system (T6SS). Hfq is an RNA chaperone that functions by stabilizing small noncoding RNAs (sRNAs) and/or facilitating base pairing between sRNAs and mRNA targets. A previous study identified sRNA 1061, which directly targets the mRNA and likely inhibits ExsA synthesis. In this study, we screened an sRNA expression library and identified sRNA 179 as an Hfq-dependent inhibitor of T3SS gene expression. Further characterization revealed that sRNA 179 inhibits the synthesis of both ExsA and Vfr. The previous finding that RsmA stimulates ExsA and Vfr synthesis suggested that sRNA 179 impacts the Gac/Rsm system. Consistent with that idea, the inhibitory activity of sRNA 179 is suppressed in a mutant lacking and , and sRNA 179 expression stimulates transcription. RsmY and RsmZ are small noncoding RNAs that sequester RsmA from target mRNAs. Our combined findings show that Hfq and sRNA 179 indirectly regulate ExsA and Vfr synthesis by reducing the available pool of RsmA, leading to reduced expression of the T3SS and cAMP-Vfr regulons. Control of gene expression by small noncoding RNA (sRNA) is well documented but underappreciated. Deep sequencing of mRNA preparations from suggests that >500 sRNAs are generated. Few of those sRNAs have defined roles in gene expression. To address that knowledge gap, we constructed an sRNA expression library and identified sRNA 179 as a regulator of the type III secretion system (T3SS) and the cAMP-Vfr regulons. The T3SS- and cAMP-Vfr-controlled genes are critical virulence factors. Increased understanding of the signals and regulatory mechanisms that control these important factors will enhance our understanding of disease progression and reveal potential approaches for therapeutic intervention.

摘要

是一种革兰氏阴性机会性病原体,可引起皮肤和软组织、呼吸道和血流感染。III 型分泌系统(T3SS)是一种重要的毒力因子。T3SS 的产生受转录因子 ExsA 控制,该转录因子激活整个 T3SS 调节子的表达。全局调节剂包括 Vfr、RsmA 和 Hfq 也有助于 T3SS 的调节。Vfr 是一种 cAMP 反应性转录因子,可激活转录。RsmA,一种 RNA 结合蛋白,可反向控制 T3SS 和 VI 型分泌系统(T6SS)的表达。Hfq 是一种 RNA 伴侣,通过稳定小非编码 RNA(sRNA)和/或促进 sRNA 与 mRNA 靶标之间的碱基配对起作用。先前的研究鉴定了 sRNA 1061,它直接靶向 mRNA,并可能抑制 ExsA 的合成。在这项研究中,我们筛选了 sRNA 表达文库,并鉴定出 sRNA 179 是 T3SS 基因表达的 Hfq 依赖性抑制剂。进一步的表征表明,sRNA 179 抑制 ExsA 和 Vfr 的合成。先前的研究表明,RsmA 刺激 ExsA 和 Vfr 的合成,表明 sRNA 179 影响 Gac/Rsm 系统。这一观点一致,sRNA 179 的抑制活性在缺乏和的突变体中受到抑制,并且 sRNA 179 的表达刺激转录。RsmY 和 RsmZ 是小非编码 RNA,可将 RsmA 与靶 mRNA 隔离。我们的综合研究结果表明,Hfq 和 sRNA 179 通过减少可用的 RsmA 池间接调节 ExsA 和 Vfr 的合成,导致 T3SS 和 cAMP-Vfr 调节子的表达减少。小非编码 RNA(sRNA)对基因表达的控制已有充分的记录,但认识不足。对的 mRNA 制剂进行深度测序表明,生成了>500 个 sRNA。其中很少有 sRNA 在基因表达中具有明确的作用。为了解决这一知识差距,我们构建了 sRNA 表达文库,并鉴定出 sRNA 179 是 III 型分泌系统(T3SS)和 cAMP-Vfr 调节子的调节剂。T3SS 和 cAMP-Vfr 控制的基因是关键的毒力因子。增加对控制这些重要因子的信号和调节机制的理解将增强我们对疾病进展的理解,并揭示潜在的治疗干预方法。

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