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F 接合转移系统与 CloDF13::Tna 质粒之间的相互作用。

Interactions between the F conjugal transfer system and CloDF13::Tna plasmids.

作者信息

Willetts N

出版信息

Mol Gen Genet. 1980;180(1):213-7. doi: 10.1007/BF00267372.

DOI:10.1007/BF00267372
PMID:6255294
Abstract

It was confirmed that all the F transfer genes required for the formation of stable mating pairs, including traN and traG, are essential for transfer of the two small multicopy plasmids ColE1 and cloDF13, whereas the traM, traI and traZ genes that are required for F conjugal DNA metabolism, are not. Differences between ColE1 and CloDF13 were that the F traD gene was needed for transfer of ColE1 but not of CloDF13, and that R100-1 efficiently transferred CloDF13 but not ColE1. A copy number mutant of CloDF13 inhibited F transfer and reduced plaque formation by the F-specific RNA phage f2, but not by Q beta or by the single-strand DNA phage f1. This phenotype suggests that the inhibition system (FinC) acts on traD, mutations in which give a similar phenotype. Hybridisation experiments with lambda tra phage DNA showed that transcription of traD was not reduced, and FinC probably inhibits function of the traD product rather than its synthesis. FinC-insensitive Flac mutants were isolated and characterised. One was shown to have an uppromoter mutation resulting in increased transcription of traJ and hence of the traY leads to Z operon including traD: the raised level of the traD product presumably then counteracted FinC inhibition.

摘要

已证实,形成稳定配对所需的所有F转移基因,包括traN和traG,对于两个小多拷贝质粒ColE1和cloDF13的转移至关重要,而F接合DNA代谢所需的traM、traI和traZ基因则并非如此。ColE1和CloDF13之间的差异在于,F traD基因是ColE1转移所必需的,但不是CloDF13转移所必需的;R100-1能有效转移CloDF13,但不能转移ColE1。CloDF13的一个拷贝数突变体抑制F转移,并减少F特异性RNA噬菌体f2形成噬菌斑,但不影响Qβ或单链DNA噬菌体f1形成噬菌斑。这种表型表明抑制系统(FinC)作用于traD,traD中的突变会产生类似的表型。用λtra噬菌体DNA进行的杂交实验表明,traD的转录没有减少,FinC可能抑制traD产物的功能而不是其合成。分离并鉴定了对FinC不敏感的Flac突变体。其中一个被证明有一个上游启动子突变,导致traJ转录增加,从而导致包括traD在内的traY至Z操纵子转录增加:traD产物水平的提高大概抵消了FinC的抑制作用。

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本文引用的文献

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Transfer-deficient cointegrates of Flac and lambda prophage.弗氏志贺菌和λ原噬菌体的转移缺陷共整合体
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Characterisation of an in vivo system for nicking at the origin of conjugal DNA transfer of the sex factor F.性因子F接合DNA转移起始位点切口的体内系统特性分析
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