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The DNA unwinding element: a novel cis-acting component that facilitates opening of the Escherichia coli replication origin.

机译:DNA解链元件:一种新型的顺式作用成分可促进大肠杆菌复制起点的打开。

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摘要

We have discovered that DNA supercoiling, in the absence of replication proteins, induces localized unwinding in the Escherichia coli replication origin (oriC) at the same sequence opened by the dnaA initiator protein. The DNA helix at the tandemly repeated, 13mer sequence is thermodynamically unstable, as evidenced by hypersensitivity to single-strand-specific nuclease in a negatively supercoiled plasmid, and demonstrated by stable DNA unwinding seen after two-dimensional gel electrophoresis of topoisomers. A replication-defective oriC mutant lacking the leftmost 13mer shows no nuclease hypersensitivity in two remaining 13mers and no detectable DNA unwinding on two-dimensional gels. The replication defect in the oriC mutant can be corrected by inserting a dissimilar DNA sequence with reduced helical stability in place of the leftmost 13mer. Thus, the helical instability of the leftmost 13mer, not the specific 13mer sequence, is essential for origin function. The rightmost 13mer exhibits helical instability but differs from the leftmost 13mer in its strict sequence conservation among related bacterial origins. The repeated 13mer region appears to serve two overlapping functions: protein recognition and helical instability. We propose that the cis-acting sequence whose helical instability is required for origin function be called the DNA unwinding element (DUE).
机译:我们已经发现,在没有复制蛋白的情况下,DNA超螺旋在dnaA启动子蛋白打开的相同序列下诱导大肠杆菌复制起点(oriC)中的局部解绕。串联重复的13mer序列的DNA螺旋是热力学不稳定的,这是由负超螺旋质粒中对单链特异性核酸酶的超敏性所证明的,并且由拓扑异构体的二维凝胶电泳后可见的稳定的DNA解旋所证明。缺少最左边的13mer的复制缺陷oriC突变体在其余两个13mer中没有核酸酶超敏反应,在二维凝胶上没有可检测到的DNA解链。 oriC突变体中的复制缺陷可以通过插入螺旋稳定性降低的不同DNA序列代替最左边的13mer来纠正。因此,最左端的13mer而不是特定的13mer序列的螺旋不稳定对于起源功能至关重要。最右端的13mer表现出螺旋不稳定,但与最左端的13mer相比,在相关细菌起源中其严格的序列保守性有所不同。重复的13mer区域似乎具有两个重叠的功能:蛋白质识别和螺旋不稳定性。我们建议将其螺旋不稳定性是起始功能所必需的顺式作用序列称为DNA解链元件(DUE)。

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