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肠球菌 PrgU 提供了额外的调节信息素诱导的可育质粒。

Enterococcal PrgU Provides Additional Regulation of Pheromone-Inducible Conjugative Plasmids.

机构信息

Department of Medical Biochemistry and Biophysics, Umeå University, Umeå, Sweden.

Department of Microbiology and Molecular Genetics, McGovern Medical School, Houston, Texas, USA.

出版信息

mSphere. 2021 Jun 30;6(3):e0026421. doi: 10.1128/mSphere.00264-21. Epub 2021 Jun 9.

Abstract

Efficient horizontal gene transfer of the conjugative plasmid pCF10 from Enterococcus faecalis depends on the expression of its type 4 secretion system (T4SS) genes, controlled by the P promoter. Transcription from the P promoter is tightly regulated, partially to limit cell toxicity caused by overproduction of PrgB, a T4SS adhesin. PrgU plays an important role in regulating this toxicity by decreasing PrgB levels. PrgU has an RNA-binding fold, prompting us to test whether PrgU exerts its regulatory control through binding of transcripts. We used a combination of methods to quantify PrgU effects on transcripts at both single-cell and population levels. PrgU function requires a specific RNA sequence within an intergenic region (IGR) about 400 bp downstream of P. PrgU interaction with the IGR reduces levels of downstream transcripts. Single-cell expression analysis showed that cells expressing decreased transcript levels more rapidly than isogenic -minus cells. PrgU bound RNA without sequence specificity, suggesting that PrgU requires a specific RNA structure or one or more host factors for selective binding . PrgU binding to its IGR target might recruit RNase(s) for targeted degradation of downstream transcripts or reduce elongation of nascent transcripts beyond the IGR. Bacteria utilize type 4 secretion systems (T4SS) to efficiently transfer DNA between donor and recipient cells, thereby spreading genes encoding antibiotic resistance as well as various virulence factors. Regulation of expression of the T4SS proteins and surface adhesins in Gram-positive bacteria is crucial, as some of these are highly toxic to the cell. The significance of our research lies in identifying the novel mechanism by which PrgU performs its delicate fine-tuning of the expression levels. As orthologs are present in various conjugative plasmids and transposons, our results are likely relevant to understanding of diverse clinically important transfer systems.

摘要

从屎肠球菌中高效水平转移的接合质粒 pCF10 依赖于其类型 4 分泌系统 (T4SS) 基因的表达,这些基因受 P 启动子控制。P 启动子的转录受到严格调控,部分原因是为了限制 T4SS 黏附素 PrgB 过表达引起的细胞毒性。PrgU 通过降低 PrgB 水平在调节这种毒性方面发挥重要作用。PrgU 具有 RNA 结合折叠结构,这促使我们测试 PrgU 是否通过结合 转录物来发挥其调节控制作用。我们使用了一系列方法来定量分析 PrgU 在单细胞和群体水平上对 转录物的影响。PrgU 功能需要 P 下游约 400bp 的基因间区 (IGR) 内的特定 RNA 序列。PrgU 与 IGR 的相互作用降低了下游转录物的水平。单细胞表达分析表明,表达 的细胞比同基因 -minus 细胞更快地降低了转录物水平。PrgU 与 RNA 结合没有序列特异性,这表明 PrgU 需要特定的 RNA 结构或一个或多个宿主因子来进行选择性结合 。PrgU 与它的 IGR 靶标结合可能会招募 RNase(s) 来靶向降解下游转录物,或者减少 IGR 下游新生转录物的延伸。细菌利用类型 4 分泌系统 (T4SS) 在供体和受体细胞之间有效地转移 DNA,从而传播编码抗生素抗性以及各种毒力因子的基因。革兰氏阳性菌中 T4SS 蛋白和表面黏附素的表达调控至关重要,因为其中一些对细胞具有高度毒性。我们研究的意义在于确定 PrgU 精细调节表达水平的新机制。由于 同源物存在于各种接合质粒和转座子中,因此我们的研究结果可能与理解各种临床重要的转移系统有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc59/8265641/2716f6ed0b27/msphere.00264-21-f001.jpg

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