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Unlinking of supercoiled DNA catenanes by type IIA topoisomerases.

机译:IIA型拓扑异构酶使超螺旋DNA链烯解链。

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It was found recently that DNA catenanes, formed during replication of circular plasmids, become positively (+) supercoiled, and the unlinking of such catenanes by type IIA topoisomerases proceeds much more efficiently than the unlinking of negatively (-) supercoiled catenanes. In an attempt to explain this striking finding we studied, by computer simulation, conformational properties of supercoiled DNA catenanes. Although the simulation showed that conformational properties of (+) and (-) supercoiled replication catenanes are very different, these properties per se do not give any advantage to (+) supercoiled over (-) supercoiled DNA catenanes for unlinking. An advantage became evident, however, when we took into account the established features of the enzymatic reaction catalyzed by the topoisomerases. The enzymes create a sharp DNA bend in the first bound DNA segment and allow for the transport of the second segment only from inside the bend to its outside. We showed that in (-) supercoiled DNA catenanes this protein-bound bent segment becomes nearly inaccessible for segments of the other linked DNA molecule, inhibiting the unlinking.
机译:最近发现,在环状质粒复制过程中形成的DNA链烯变成正(+)超螺旋,并且通过IIA型拓扑异构酶进行的此类链的解链比负(-)超螺旋链的解链更为有效。为了解释这一惊人发现,我们通过计算机模拟研究了超螺旋DNA链烯的构象性质。尽管模拟显示(+)和(-)超螺旋复制链的构象性质非常不同,但与(-)超螺旋DNA链相比,这些性质本身对(+)超螺旋的链没有任何优势。但是,当我们考虑拓扑异构酶催化的酶促反应的既定特征时,优势就变得显而易见。这些酶在第一个结合的DNA片段中产生了一个尖锐的DNA弯曲,仅允许第二个片段从弯曲内部向其外部运输。我们显示,在(-)超螺旋DNA链烯中,该蛋白质结合的弯曲片段几乎变得无法连接到其他链接的DNA分子的片段,从而抑制了未链接。

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