首页> 美国卫生研究院文献>Nucleic Acids Research >The integration host factor of Escherichia coli binds to multiple sites at plasmid R6K gamma origin and is essential for replication.
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The integration host factor of Escherichia coli binds to multiple sites at plasmid R6K gamma origin and is essential for replication.

机译:大肠杆菌的整合宿主因子与质粒R6Kγ起源的多个位点结合对于复制至关重要。

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摘要

Examination of the effect of the himA and himD mutants of E. coli on the maintenance of plasmid R6K has revealed that the gamma origin-containing replicons cannot be established in any of the mutants deficient in the production of E. coli Integration Host Factor (IHF). Contrary, the R6K derivatives containing other origins of the plasmid (alpha and/or beta) replicate in a host lacking functional IHF protein. We show that IHF protein binds specifically to a segment of the replication region which is essential for the activity of all three R6K origins. Mapping the IHF binding sequence with neocarzinostatin showed that the protein protects three segments of the origin: two strong binding sites reside within an AT-rich block, while the third, considerably weaker site is separated from the other two by a cluster of the seven 22 bp direct repeats. These seven repeats have been shown previously to bind the R6K-encoded initiator protein pi. We also demonstrate that the establishment of pi-origin complexes prior to IHF addition prevents the binding of the IHF protein to the gamma origin. The binding sequences of IHF and pi proteins do not overlap, therefore, we propose that the binding of pi protein alters the structure of the DNA and thereby prevents the subsequent binding of IHF protein.
机译:检查大肠杆菌的himA和himD突变体对维持质粒R6K的作用已发现,在任何缺乏大肠杆菌整合宿主因子(IHF)产生的突变体中,都无法建立含伽马来源的复制子。 )。相反,含有质粒其他来源(α和/或β)的R6K衍生物在缺乏功能性IHF蛋白的宿主中复制。我们表明,IHF蛋白特异性结合复制区域的一部分,这对于所有三个R6K起源的活动必不可少。将IHF结合序列与新卡他汀抑制素作图表明,该蛋白保护起源的三个片段:两个强结合位点位于富含AT的嵌段内,而第三个弱结合位点则由七个22的簇与其他两个分开bp直接重复。先前已显示这七个重复序列结合了R6K编码的起始蛋白pi。我们还证明,在添加IHF之前先建立pi-origin复合物可防止IHF蛋白与伽玛来源的结合。 IHF和pi蛋白的结合序列不重叠,因此,我们提出pi蛋白的结合会改变DNA的结构,从而阻止后续IHF蛋白的结合。

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