An sRNA overexpression library reveals AbnZ as a negative regulator of an essential translocation module in Caulobacter crescentus

被引:0
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作者
Velasco-Gomariz, Manuel [1 ]
Sulzer, Johannes [2 ,3 ]
Faber, Franziska [2 ,3 ]
Froehlich, Kathrin S. [1 ,4 ]
机构
[1] Friedrich Schiller Univ, Inst Microbiol, D-07743 Jena, Germany
[2] Julius Maximilians Univ Wurzburg, Inst Hyg & Microbiol, Fac Med, D-97080 Wurzburg, Germany
[3] Helmholtz Ctr Infect Res HZI, Helmholtz Inst RNA Based Infect Res HIRI, D-97080 Wurzburg, Germany
[4] Friedrich Schiller Univ, Microverse Cluster, D-07743 Jena, Germany
关键词
POSTTRANSCRIPTIONAL REGULATION; NONCODING RNAS; STRESS; METABOLISM; SEQUENCE; FEATURES; SYSTEM; CYAR;
D O I
10.1093/nar/gkae1139
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Small RNAs (sRNAs) play a crucial role in modulating target gene expression through short base-pairing interactions and serve as integral components of many stress response pathways and regulatory circuits in bacteria. Transcriptome analyses have facilitated the annotation of dozens of sRNA candidates in the ubiquitous environmental model bacterium Caulobacter crescentus, but their physiological functions have not been systematically investigated so far. To address this gap, we have established CauloSOEP, a multi-copy plasmid library of C. crescentus sRNAs, which can be studied in a chosen genetic background and under select conditions. Demonstrating the power of CauloSOEP, we identified sRNA AbnZ to impair cell viability and morphology. AbnZ is processed from the 3 ' end of the polycistronic abn mRNA encoding the tripartite envelope-spanning efflux pump AcrAB-NodT. A combinatorial approach revealed the essential membrane translocation module TamAB as a target of AbnZ, implying that growth inhibition by AbnZ is linked to repression of this system.
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页数:15
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