Trigueros Sonia, Salceda Javier, Bermúdez Ignacio, Fernández Xavier, Roca Joaquim
Instituto de Biología Molecular de Barcelona, Consejo Superior de Investigaciones Científicas, Barcelona 08034, Spain.
J Mol Biol. 2004 Jan 16;335(3):723-31. doi: 10.1016/j.jmb.2003.11.011.
Type-IIA topoisomerases consume ATP as they catalyse the interconversion of DNA topoisomers by transporting one DNA segment through a transient break in another. It remains unclear how their activity simplifies the topology of DNA below equilibrium values. Here we report that eukaryotic topoisomerase II narrows the thermal distribution of DNA supercoils, by mainly removing negative DNA crossings. Surprisingly, this asymmetry in supercoil removal is not due to deformation of the DNA before strand passage. Topoisomerase II neither bends nor alters the helical conformation of the interacting DNA. Rather, it appears to interact with a third DNA segment, in addition to the gated and the transported segments. Remarkably, the simultaneous interaction with three DNA segments accounts for the asymmetric removal of supercoils in relaxed DNA and gives a clue to how topoisomerase II simplifies the topology of DNA against the thermal drive.
IIA型拓扑异构酶在催化DNA拓扑异构体的相互转化时会消耗ATP,它们通过将一个DNA片段穿过另一个片段中的瞬时断裂来实现这一转化。目前尚不清楚它们的活性是如何将DNA的拓扑结构简化到平衡值以下的。在这里,我们报告真核生物拓扑异构酶II通过主要去除负向DNA交叉来缩小DNA超螺旋的热分布。令人惊讶的是,超螺旋去除中的这种不对称性并非由于链通过前DNA的变形。拓扑异构酶II既不弯曲也不改变相互作用DNA的螺旋构象。相反,除了门控片段和转运片段外,它似乎还与第三个DNA片段相互作用。值得注意的是,与三个DNA片段的同时相互作用解释了松弛DNA中超螺旋的不对称去除,并为拓扑异构酶II如何克服热驱动力简化DNA拓扑结构提供了线索。