Vologodskii Alexander
Department of Chemistry, New York University, New York, NY 10003, USA.
Nucleic Acids Res. 2009 Jun;37(10):3125-33. doi: 10.1093/nar/gkp250. Epub 2009 Apr 21.
It was discovered 12 years ago that type IIA topoisomerases can simplify DNA topology--the steady-state fractions of knots and links created by the enzymes are many times lower than the corresponding equilibrium fractions. Though this property of the enzymes made clear biological sense, it was not clear how small enzymes could selectively change the topology of very large DNA molecules, since topology is a global property and cannot be determined by a local DNA-protein interaction. A few models, suggested to explain the phenomenon, are analyzed in this review. We also consider experimental data that both support and contravene these models.
12年前人们发现,IIA型拓扑异构酶能够简化DNA拓扑结构——由这些酶产生的结和连环的稳态分数比相应的平衡分数低很多倍。尽管酶的这一特性具有明确的生物学意义,但尚不清楚小型酶如何能够选择性地改变非常大的DNA分子的拓扑结构,因为拓扑结构是一种全局特性,无法由局部的DNA-蛋白质相互作用来决定。本文综述分析了一些为解释该现象而提出的模型。我们还考量了支持和反驳这些模型的实验数据。