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首页> 外文期刊>Journal of Molecular Biology >Monomer/dimer ratios of replication protein modulate the DNAstrand-opening in a replication origin
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Monomer/dimer ratios of replication protein modulate the DNAstrand-opening in a replication origin

机译:复制蛋白的单体/二聚体比例调节复制起点中的DNAstrand-opening

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摘要

DNA opening is an essential step in the initiation of replication via the Cairns mode of replication. The opening reaction was investigated in a gamma ori system by using hyperactive variants of plasmid R6K-encoded initiator protein, pi. Reactivity to KMnO4 (indicative of opening) within gamma ori DNA occurred in both strands of a superhelical template upon the combined addition of wt pi, DnaA and integration host factor (IHF), each protein known to specifically bind gamma ori. IHF, examined singly, enhanced reactivity to KMnO4. The IHF-dependent reactive residues, however, are distinct from those dependent on pi (wt and hyperactive variants). Remarkably, the DNA helix opening does not require IHF and/or DnaA when hyperactive variants of pi were used instead of wt protein. We present three lines of evidence consistent with the hypothesis that DNA strand separation is facilitated by pi monomers despite the fact that both monomers and dimers of the protein can bind to iterons (pi binding sites). Taken together, our data suggest that pi elicits its ability to modulate plasmid copy number at the DNA helix-opening step.
机译:通过凯恩斯复制模式,DNA的开放是复制过程中必不可少的步骤。通过使用质粒R6K编码的启动子蛋白pi的高活性变异体在γori系统中研究了开放反应。结合添加wt pi,DnaA和整合宿主因子(IHF)后,在超螺旋模板的两条链中都发生了与γori DNA中的KMnO4的反应(指示打开),每种蛋白质都已知与γori特异性结合。单独检查,IHF增强了对KMnO4的反应性。但是,依赖IHF的反应性残基与依赖pi的残基不同(wt和hyperactive变体)。值得注意的是,当使用pi的高活性变体代替wt蛋白时,DNA螺旋开口不需要IHF和/或DnaA。尽管存在蛋白质的单体和二聚体都可以结合到Iteron(pi结合位点)的事实,但我们提供了三条证据与pi单体促进DNA链分离的假设相符。两者合计,我们的数据表明pi激发其在DNA螺旋打开步骤调节质粒拷贝数的能力。

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