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合作相互作用控制广宿主范围质粒RK2的接合转移:TrbA操纵子微小变化的完整效应取决于KorB。

Co-operative interactions control conjugative transfer of broad host-range plasmid RK2: full effect of minor changes in TrbA operator depends on KorB.

作者信息

Bingle Lewis E H, Zatyka Malgorzata, Manzoor Susan E, Thomas Christopher M

机构信息

School of Biosciences, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK.

出版信息

Mol Microbiol. 2003 Aug;49(4):1095-108. doi: 10.1046/j.1365-2958.2003.03620.x.

Abstract

A network of circuits, with KorB and TrbA as key regulators, controls genes for conjugative transfer of broad host range plasmid RK2. To assess the importance of the TrbA regulon, mutational analysis was applied to the TrbA operator at the trbB promoter and then to other TrbA-regulated promoters in the tra region. All identified TrbA operators are submaximal; in the case of trbBp, a G to A transition that made the operator core a perfect palindrome increased repression by about 50% compared to the wild type. When this change was introduced into the RK2 genome, decreases in transfer frequency of up to three orders of magnitude were observed, with bigger effects when Escherichia coli was the donor compared to Pseudomonas putida. Western blotting showed a significant decrease in Trb protein levels. These effects were much greater than the effect of the mutation on repression by TrbA alone. When KorB was introduced into the reporter system, the effects were closer to those observed in the whole RK2 context. These results indicate that co-operativity, previously observed between TrbA and KorB, allows big changes in transfer gene expression to result from small changes in individual regulator activities.

摘要

以KorB和TrbA作为关键调控因子的一个回路网络,控制着广宿主范围质粒RK2接合转移的相关基因。为了评估TrbA调控子的重要性,对trbB启动子处的TrbA操纵子进行了突变分析,随后又对tra区域中其他受TrbA调控的启动子进行了突变分析。所有鉴定出的TrbA操纵子都不是最佳的;就trbBp而言,一个从G到A的转变使操纵子核心成为一个完美的回文序列,与野生型相比,阻遏作用提高了约50%。当将此变化引入RK2基因组时,观察到转移频率下降了多达三个数量级,与恶臭假单胞菌相比,当大肠杆菌作为供体时影响更大。蛋白质免疫印迹法显示Trb蛋白水平显著降低。这些影响远大于该突变单独对TrbA阻遏作用的影响。当将KorB引入报告系统时,其影响更接近于在整个RK2环境中观察到的结果。这些结果表明,先前在TrbA和KorB之间观察到的协同作用,使得单个调控因子活性的微小变化能导致转移基因表达发生巨大变化。

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