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首页> 外文期刊>Journal of Molecular Biology >Lac and lambda repressors relieve silencing of the Escherichia coli bgl promotor. Activation by alteration of a repressing nucleoprotein complex
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Lac and lambda repressors relieve silencing of the Escherichia coli bgl promotor. Activation by alteration of a repressing nucleoprotein complex

机译:Lac和λ阻遏物可缓解大肠杆菌bgl启动子的沉默。通过改变抑制性核蛋白复合物激活

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摘要

The Escherichia coli bgl promoter is kept in a repressed state by silencer sequences which flank the promoter and by the histone-like protein H-NS. Silencing of the bgl promoter is likely due to the formation of a repressing nucleoprotein complex of which H-NS is an essential component. Here, we show that silencing is abolished by the binding of Lac or lambda repressors to their respective operators that were inserted within the bgl upstream silencer. Efficient activation of bgl operon transcription by Lac and lambda repressors was independent of the position and phasing of the operators with respect to the promoter. Activation by Lac and lambda repressors as shown here is unprecedented. We conclude that the activation of bgl transcription by both repressors is achieved by a novel mechanism, that is by alteration of the repressing nucleoprotein complex rather than by protein-protein interactions with RNA polymerase and the catabolite activator protein, CAP. (C) 1998 Academic Press. [References: 59]
机译:大肠杆菌bgl启动子通过位于启动子侧面的沉默子序列和组蛋白样蛋白H-NS保持在受阻状态。 bgl启动子的沉默可能是由于形成了一种抑制性核蛋白复合物,其中H-NS是必需成分。在这里,我们显示通过将Lac或lambda阻遏物与其各自的插入bgl上游消音器的操纵子的结合而消除了沉默。 Lac和lambda阻遏物对bgl操纵子转录的有效激活独立于操纵子相对于启动子的位置和阶段。如图所示,Lac和lambda阻遏物的激活是前所未有的。我们得出的结论是,两个阻遏物均可通过一种新颖的机制来实现bgl转录的激活,即通过改变阻遏核蛋白复合物而不是通过蛋白质与RNA聚合酶和分解代谢物激活蛋白CAP的相互作用来实现。 (C)1998年学术出版社。 [参考:59]

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