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Dynamic Escherichia coli SeqA complexes organize the newly replicated DNA at a considerable distance from the replisome

机译:动态大肠杆菌SeqA复合体在距复制体相当远的距离处组织新复制的DNA

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摘要

The Escherichia coli SeqA protein binds to newly replicated, hemimethylated DNA behind replication forks and forms structures consisting of several hundred SeqA molecules bound to about 100 kb of DNA. It has been suggested that SeqA structures either direct the new sister DNA molecules away from each other or constitute a spacer that keeps the sisters together. We have developed an image analysis script that automatically measures the distance between neighboring foci in cells. Using this tool as well as direct stochastic optical reconstruction microscopy (dSTORM) we find that in cells with fluorescently tagged SeqA and replisome the sister SeqA structures were situated close together (less than about 30 nm apart) and relatively far from the replisome (on average 200–300 nm). The results support the idea that newly replicated sister molecules are kept together behind the fork and suggest the existence of a stretch of DNA between the replisome and SeqA which enjoys added stabilization. This could be important in facilitating DNA transactions such as recombination, mismatch repair and topoisomerase activity. In slowly growing cells without ongoing replication forks the SeqA protein was found to reside at the fully methylated origins prior to initiation of replication.
机译:大肠杆菌SeqA蛋白在复制叉后与新复制的半甲基化DNA结合,并形成由数百个SeqA分子结合约100 kb DNA组成的结构。已经提出,SeqA结构或者使新的姐妹DNA分子彼此远离,或者构成使姐妹保持在一起的间隔物。我们已经开发了一种图像分析脚本,可以自动测量细胞中相邻病灶之间的距离。使用该工具以及直接随机光学重建显微镜(dSTORM),我们发现在带有荧光标记SeqA和复制体的细胞中,姐妹SeqA结构彼此靠近(相距小于30 nm),并且相对于复制体相对较远(平均200–300 nm)。结果支持了新复制的姐妹分子在叉子后面保持在一起的想法,并表明在复制体和SeqA之间存在一段DNA片段,该片段具有增强的稳定性。这对促进DNA交易(例如重组,错配修复和拓扑异构酶活性)可能很重要。在没有进行中的复制叉的缓慢生长的细胞中,发现SeqA蛋白在复制开始之前位于完全甲基化的起点。

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