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酵母DNA拓扑异构酶II去除超螺旋和解开连环的概率。

The probabilities of supercoil removal and decatenation by yeast DNA topoisomerase II.

作者信息

Roca J, Wang J C

机构信息

Department of Molecular and Cellular Biology, Harvard University, Cambridge, Massachusetts 02138, USA.

出版信息

Genes Cells. 1996 Jan;1(1):17-27. doi: 10.1046/j.1365-2443.1996.01001.x.

Abstract

BACKGROUND

In yeast a single type II DNA topoisomerase is involved in both the removal of DNA supercoils and the unlinking of intertwined pairs of newly replicated chromosomes or plasmids; in bacteria, two type II enzymes, DNA gyrase and DNA topoisomerase IV, function separately in the passage of DNA segments in cis and in trans. To deduce the molecular characteristics of these enzyme-mediated reactions, the efficiencies of supercoil removal and decatenation by the yeast enzyme upon the addition of a nonhydrolysable ATP analogue were determined.

RESULTS

The probability that a bound enzyme transports a DNA segment in cis increases with positive or negative supercoiling of the DNA, and transport is nearly quantitative at high degrees of supercoiling. The relative probabilities of transporting a contiguous and noncontiguous DNA segment by a yeast enzyme bound to one member of a singly linked pair of 3.6-kb rings were calculated from the observed efficiency of decatenation. When the enzyme-bound ring is highly supercoiled, transport of a noncontiguous segment is more probable than a contiguous one.

CONCLUSION

A DNA-bound yeast enzyme has no intrinsic bias in its selection of a contiguous or noncontiguous DNA segment for transport, and the selection is determined by DNA conformations. For the singly linked dimeric catenane studied, a high degree of supercoiling of the enzyme-bound DNA does not make supercoil removal more favourable than decatenation. In the case of bacterial gyrase, however, wrapping of a DNA segment around the enzyme is expected to strongly favour the transport of a contiguous segment.

摘要

背景

在酵母中,单一的II型DNA拓扑异构酶参与DNA超螺旋的去除以及新复制的染色体或质粒相互缠绕对的解链;在细菌中,两种II型酶,即DNA促旋酶和DNA拓扑异构酶IV,分别在顺式和反式DNA片段的通过中发挥作用。为了推断这些酶介导反应的分子特征,测定了在添加不可水解的ATP类似物后酵母酶去除超螺旋和解链的效率。

结果

结合的酶顺式转运DNA片段的概率随着DNA的正超螺旋或负超螺旋而增加,并且在高度超螺旋时转运几乎是定量的。根据观察到的解链效率,计算了与一对3.6 kb单链环中的一个成员结合的酵母酶转运连续和非连续DNA片段的相对概率。当与酶结合的环高度超螺旋时,非连续片段的转运比连续片段更有可能。

结论

结合DNA的酵母酶在选择连续或非连续DNA片段进行转运时没有内在偏好,这种选择由DNA构象决定。对于所研究的单链二聚连环体,与酶结合的DNA的高度超螺旋并不会使超螺旋去除比解链更有利。然而,在细菌促旋酶的情况下,预计DNA片段围绕酶的缠绕会强烈有利于连续片段的转运。

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