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首页> 外文期刊>Plasmid: An International Journal Devoted to Extrachromosomal Gene Systems >Structural analysis of the Anti-Q-Qs interaction: RNA-mediated regulation of E. faecalis plasmid pCF10 conjugation.
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Structural analysis of the Anti-Q-Qs interaction: RNA-mediated regulation of E. faecalis plasmid pCF10 conjugation.

机译:抗Q-Qs相互作用的结构分析:RNA介导的粪肠球菌质粒pCF10偶联调节。

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摘要

Conjugation of the E. faecalis plasmid pCF10 is triggered in response to peptide sex pheromone cCF10 produced by potential recipients. Regulation of this response is complex and multi-layered and includes a small regulatory RNA, Anti-Q that participates in a termination/antitermination decision controlling transcription of the conjugation structural genes. In this study, the secondary structure of the Anti-Q transcript and its sites of interaction with its target, Qs, were determined. The primary site of interaction occurred at a centrally-located loop whose sequence showed high variability in analogous molecules on other pheromone-responsive plasmids. This loop, designated the specificity loop, was demonstrated to be important but not sufficient for distinguishing between Qs molecules from pCF10 and another pheromone-responsive plasmid pAD1. A loop 5' from the specificity loop which carries a U-turn motif played no demonstrable role in Anti-Q-Qs interaction or regulation of the termination/antitermination decision. These results provide direct evidence for a critical role of Anti-Q-Qs interactions in posttranscriptional regulation of pCF10 transfer functions.
机译:粪肠球菌质粒pCF10的缀合响应于潜在受体产生的肽性信息素cCF10而触发。该反应的调节是复杂且多层的,并且包括一个小的调节RNA,即Anti-Q,参与终止/抗终止决定,该决定控制缀合结构基因的转录。在这项研究中,确定了抗Q转录本的二级结构及其与靶标Qs相互作用的位点。相互作用的主要位点发生在位于中央的环上,该环的序列在其他信息素应答质粒上的类似分子中显示出高度的变异性。该环称为特异性环,被证明是重要的,但不足以区分来自pCF10的Qs分子和另一个信息素应答质粒pAD1。来自特异性环的带有掉头基序的环5'在抗Q-Qs相互作用或终止/抗终止决定的调节中没有起到可证明的作用。这些结果提供了直接的证据证明抗Q Qs相互作用在pCF10传递功能的转录后调控中的关键作用。

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