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首页> 外文期刊>Journal of bacteriology >Three distinct chromosome replication states are induced by increasing concentrations of DnaA protein in Escherichia coli.
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Three distinct chromosome replication states are induced by increasing concentrations of DnaA protein in Escherichia coli.

机译:通过增加大肠杆菌中DnaA蛋白的浓度来诱导三个不同的染色体复制状态。

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摘要

The DnaA protein concentration in Escherichia coli was increased above the wild-type level by inducing a lacP-controlled dnaA gene located on a plasmid. In these cells with different DnaA protein levels, we measured several parameters: dnaA gene expression; cell size, amount of DNA per cell, and number of origins per cell by flow cytometry; and origin-to-terminus ratio and the frequencies of five other markers on the chromosome by Southern hybridization. The response of the cells to higher levels of DnaA protein could be divided into three states. From the normal level to a level 1.5-fold higher, DnaA protein had little effect on dnaA gene expression and the rate of DNA replication but led to nearly proportional increases in DNA and origin concentrations. Between 1.5- and 3-fold, the normal DnaA protein concentration, dnaA gene expression was gradually decreased. In this interval, the origin concentration increased significantly; however, the replication rate was severely affected, becoming slower--especially near the origin--the higher the DnaA protein concentration, and as a result, the DNA concentration was constant. Further increases in the DnaA protein concentration did not lead to an increased origin concentration. Thus, the initiation mass was set by the DnaA protein from the normal level to an at least twofold-increased level, but the increased initiation did not lead to a large increase in the amount of DNA per unit of mass because of the inhibition of replication fork velocity.
机译:通过诱导位于质粒上的lacP控制的dnaA基因,大肠杆菌中的DnaA蛋白浓度增加到野生型水平以上。在这些具有不同DnaA蛋白水平的细胞中,我们测量了几个参数:dnaA基因表达;细胞大小,每个细胞的DNA量以及通过流式细胞仪检测的每个细胞的起源数; Southern杂交检测染色体上的始端比和其他五个标记的频率。细胞对更高水平的DnaA蛋白的反应可分为三种状态。从正常水平到高1.5倍,DnaA蛋白对dnaA基因表达和DNA复制速率几乎没有影响,但导致DNA和来源浓度几乎成比例增加。在1.5至3倍之间,正常的DnaA蛋白浓度,dnaA基因表达逐渐降低。在此间隔内,原产地浓度显着增加。然而,复制速率受到严重影响,变得更慢-特别是在起点附近-DnaA蛋白浓度更高,结果DNA浓度恒定。 DnaA蛋白浓度的进一步增加并未导致起始浓度的增加。因此,通过DnaA蛋白将起始质量设定为从正常水平到至少两倍增加的水平,但是增加的起始并没有由于抑制复制而导致每单位质量DNA的大量增加。货叉速度。

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