Krüger R, Konieczny I, Filutowicz M
Department of Bacteriology, University of Wisconsin, Madison, WI 53706, USA.
J Mol Biol. 2001 Mar 9;306(5):945-55. doi: 10.1006/jmbi.2000.4426.
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.
DNA解旋是通过凯恩斯复制模式起始复制的关键步骤。在γ ori系统中,利用质粒R6K编码的起始蛋白pi的高活性变体研究了解旋反应。在超螺旋模板的两条链中,当同时添加野生型pi、DnaA和整合宿主因子(IHF)时,γ ori DNA内对高锰酸钾的反应性(表明解旋)出现,已知每种蛋白质都能特异性结合γ ori。单独检测时,IHF增强了对高锰酸钾的反应性。然而,依赖IHF的反应性残基与依赖pi(野生型和高活性变体)的反应性残基不同。值得注意的是,当使用pi的高活性变体而非野生型蛋白时,DNA螺旋解旋不需要IHF和/或DnaA。我们提供了三条证据,支持以下假设:尽管该蛋白的单体和二聚体都能与重复序列(pi结合位点)结合,但pi单体促进了DNA链的分离。综上所述,我们的数据表明,pi在DNA螺旋解旋步骤发挥其调节质粒拷贝数的能力。