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首页> 外文期刊>Environmental microbiology >The CarD/CarG regulatory complex is required for the action of several members of the large set of Myxococcus xanthus extracytoplasmic function σ factors
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The CarD/CarG regulatory complex is required for the action of several members of the large set of Myxococcus xanthus extracytoplasmic function σ factors

机译:CarD / CarG调节复合物是大型粘多糖球菌胞浆外功能σ因子的几个成员的作用所必需的

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摘要

Extracytoplasmic function (ECF) σ factors are critical players in signal transduction networks involved in bacterial response to environmental changes. The Myxococcus xanthus genome reveals ~45 putative ECF-σ factors, but for the overwhelming majority, the specific signals or mechanisms for selective activation and regulation remain unknown. One wellstudied ECF-σ, CarQ, binds to its anti-σ, CarR, and is inactive in the dark but drives its own expression from promoter P_(QRS) on illumination. This requires the CarD/CarG complex, the integration host factor (IHF) and a specific CarD-binding site upstream of P_(QRS). Here, we show that DdvS, a previously uncharacterized ECF-σ, activates its own expression in a CarD/CarG-dependent manner but is inhibited when specifically bound to the N-terminal zincbinding anti-σ domain of its cognate anti-σ, DdvA. Interestingly, we find that the autoregulatory action of 11 other ECF-σ factors studied here depends totally or partially on CarD/CarG but not IHF. In silico analysis revealed possible CarD-binding sites that may be involved in direct regulation by CarD/CarG of target promoter activity. CarD/CarG-linked ECF-σ regulation likely recurs in other myxobacteria with CarD/CarG orthologous pairs and could underlie, at least in part, the global regulatory effect of the complex on M. xanthus gene expression.
机译:细胞外功能(ECF)σ因子是参与细菌对环境变化的反应的信号转导网络的关键参与者。黄色粘球菌基因组揭示了〜45个推定的ECF-σ因子,但对于绝大多数人而言,选择性激活和调节的特定信号或机制仍不清楚。一个经过充分研究的ECF-σCarQ与其抗σCarR结合,并且在黑暗中不活跃,但在照明下由启动子P_(QRS)驱动其自身表达。这需要CarD / CarG复合体,整合宿主因子(IHF)和P_(QRS)上游的特定CarD结合位点。在这里,我们显示DdvS(先前未表征的ECF-σ)以CarD / CarG依赖性方式激活其自身的表达,但在与其同源抗σDdvA的N端锌结合抗σ结构域特异性结合时受到抑制。有趣的是,我们发现这里研究的其他11个ECF-σ因子的自调节作用完全或部分取决于CarD / CarG,而不取决于IHF。计算机分析表明,可能的CarD结合位点可能参与了CarD / CarG对靶启动子活性的直接调控。 CarD / CarG连锁的ECF-σ调节可能会在其他带有CarD / CarG直系同源对的黏菌中重现,并且可能至少部分地取决于该复合物对黄腐支原体基因表达的整体调节作用。

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