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Cnr interferes with dimerization of the replication protein α in phage-plasmid P4

机译:Cnr干扰二聚化 蛋白在噬菌体质粒中的表达 P4

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摘要

DNA replication of phage-plasmid P4 in its host Escherichia coli depends on its replication protein α. In the plasmid state, P4 copy number is controlled by the regulator protein Cnr (copy number regulation). Mutations in α (αcr) that prevent regulation by Cnr cause P4 over-replication and cell death. Using the two-hybrid system in Saccharomyces cerevisiae and a system based on λ immunity in E.coli for in vivo detection of protein–protein interactions, we found that: (i) α protein interacts with Cnr, whereas αcr proteins do not; (ii) both α–α and αcr–αcr interactions occur and the interaction domain is located within the C-terminal of α; (iii) Cnr–Cnr interaction also occurs. Using an in vivo competition assay, we found that Cnr interferes with both α–α and αcr–αcr dimerization. Our data suggest that Cnr and α interact in at least two ways, which may have different functional roles in P4 replication control.
机译:噬菌体质粒P4在其宿主大肠杆菌中的DNA复制取决于其复制蛋白α。在质粒状态下,P4拷贝数由调节蛋白Cnr控制(拷贝数调节)。阻止Cnr调控的α突变(α cr )会导致P4过度复制和细胞死亡。使用酿酒酵母中的双杂交系统和基于大肠杆菌中λ免疫力的系统进行体内蛋白质-蛋白质相互作用的检测,我们发现:(i)α蛋白质与Cnr相互作用,而α cr < / sup>蛋白质不; (ii)发生α–α和α cr –α cr 相互作用,且相互作用域位于α的C端; (iii)Cnr–Cnr相互作用也会发生。通过体内竞争分析,我们发现Cnr会干扰α–α和α cr –α cr 二聚体。我们的数据表明Cnr和α至少以两种方式相互作用,这可能在P4复制控制中具有不同的功能角色。

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