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噬菌体μ溶原性阻遏的调控

Control of bacteriophage mu lysogenic repression.

作者信息

Ranquet Caroline, Toussaint Ariane, de Jong Hidde, Maenhaut-Michel Geneviève, Geiselmann Johannes

机构信息

Laboratoire du Contrôle de l'Expression Génique, Institut Jean Roget-Faculté de Médecine-Pharmacie, Domaine de la Merci, F-38700 La Tronche, France.

出版信息

J Mol Biol. 2005 Oct 14;353(1):186-95. doi: 10.1016/j.jmb.2005.08.015.

Abstract

The transposable and temperate phage Mu infects Escherichia coli where it can enter the lytic life-cycle or reside as a repressed and integrated prophage. The repressor protein Rep is the key element in the lysis-lysogeny decision. We have analyzed the fate of Rep in different mutants by Western blotting under two conditions that can induce a lysogen: high temperature and stationary phase. We show that, unexpectedly, Rep accumulates under all conditions where the prophage is completely derepressed, and that this accumulation is ClpX-dependent. An analysis of the degradation kinetics shows that Rep is a target of two protease systems: inactivation of either the clpP or lon gene results in a stabilization of Rep. Such a reaction scheme explains the counterintuitive observation that derepression is correlated with high repressor concentration. We conclude that under all conditions of phage induction the repressor is sequestered in a non-active form. A quantitative simulation accounts for our experimental data. It provides a model that captures the essential features of Mu induction and explains some of the mechanisms by which the physiological signals affecting the lysis-lysogeny decision converge onto Rep.

摘要

可转座的温和噬菌体Mu感染大肠杆菌后,它可以进入裂解生命周期,也可以作为受抑制的整合原噬菌体存在。阻遏蛋白Rep是裂解-溶原决定的关键因素。我们通过蛋白质免疫印迹法,在两种可诱导溶原菌的条件下(高温和稳定期),分析了不同突变体中Rep的命运。我们发现,出乎意料的是,在原噬菌体完全去阻遏的所有条件下,Rep都会积累,并且这种积累依赖于ClpX。对降解动力学的分析表明,Rep是两种蛋白酶系统的作用靶点:clpP或lon基因的失活都会导致Rep的稳定。这样的反应模式解释了去阻遏与高阻遏物浓度相关这一违反直觉的观察结果。我们得出结论,在噬菌体诱导的所有条件下,阻遏物都以无活性形式被隔离。定量模拟解释了我们的实验数据。它提供了一个模型,该模型抓住了Mu诱导的基本特征,并解释了一些影响裂解-溶原决定的生理信号汇聚到Rep上的机制。

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