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真核生物拓扑异构酶通过优先与DNA交叉相互作用来识别核酸拓扑结构。

Eukaryotic topoisomerases recognize nucleic acid topology by preferentially interacting with DNA crossovers.

作者信息

Zechiedrich E L, Osheroff N

机构信息

Department of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN 37232-0146.

出版信息

EMBO J. 1990 Dec;9(13):4555-62. doi: 10.1002/j.1460-2075.1990.tb07908.x.

Abstract

Eukaryotic topoisomerases recognize DNA topology and preferentially react with positively or negatively supercoiled molecules over relaxed substrates. To elucidate the mechanism of this recognition, we examined the interaction of topoisomerases with DNA by electron microscopy. Under all conditions employed, approximately 90% of the bound type I or II enzyme was observed at points of helix--helix juxtaposition on negatively supercoiled plasmids which contained as few as four crossovers. Recognition was independent of torsional stress, as enzyme molecules were also found at crossovers on linear DNA. Since juxtaposed helices are more prevalent in supercoiled compared with relaxed nucleic acids, we propose that eukaryotic topoisomerases I and II recognize underwound or overwound substrates by interacting preferentially with DNA crossovers. This may represent a general mechanism for the recognition of DNA topology by proteins.

摘要

真核生物拓扑异构酶能够识别DNA拓扑结构,并且相较于松弛的底物,它们更倾向于与正超螺旋或负超螺旋分子发生反应。为了阐明这种识别机制,我们通过电子显微镜研究了拓扑异构酶与DNA的相互作用。在所有使用的条件下,在含有少至四个交叉点的负超螺旋质粒的螺旋 - 螺旋并列处,观察到约90%的结合的I型或II型酶。识别与扭转应力无关,因为在线性DNA的交叉点处也发现了酶分子。由于与松弛的核酸相比,并列的螺旋在超螺旋中更为普遍,我们提出真核生物拓扑异构酶I和II通过优先与DNA交叉点相互作用来识别解旋或过度缠绕的底物。这可能代表了蛋白质识别DNA拓扑结构的一种普遍机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aade/552253/56fe666d3a32/emboj00240-0338-a.jpg

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