CNRS UMR7284/INSERM U1081, Institute for Research on Cancer and Aging, Nice (IRCAN), Faculty of Medicine, University Côte d'Azur, 06107 Nice, France.
Simpson Querrey Institute, 303 E Superior, Chicago, IL 60611, USA.
Cells. 2024 Aug 15;13(16):1361. doi: 10.3390/cells13161361.
Linear unconstrained DNA cannot harbor supercoils since these supercoils can diffuse and be eliminated by free rotation of the DNA strands at the end of the molecule. Mammalian telomeres, despite constituting the ends of linear chromosomes, can hold supercoils and be subjected to topological stress. While negative supercoiling was previously observed, thus proving the existence of telomeric topological constraints, positive supercoils were never probed due to the lack of an appropriate tool. Indeed, the few tools available currently could only investigate unwound (Trioxsalen) or overwound (GapR) DNA topology (variations in twist) but not the variations in writhe (supercoils and plectonemes). To address this question, we have designed innovative tools aimed at analyzing both positive and negative DNA writhe in cells. Using them, we could observe the build-up of positive supercoils following replication stress and inhibition of Topoisomerase 2 on telomeres. TRF2 depletion caused both telomere relaxation and an increase in positive supercoils while the inhibition of Histone Deacetylase I and II by TSA only caused telomere relaxation. Moving outside telomeres, we also observed a build-up of positive supercoils on the FRA3B fragile site following replication stress, suggesting a topological model of DNA fragility for this site.
线性无约束的 DNA 不能容纳超螺旋,因为这些超螺旋可以扩散,并通过分子末端 DNA 链的自由旋转而被消除。尽管哺乳动物端粒构成了线性染色体的末端,但它们可以保持超螺旋并承受拓扑压力。虽然以前已经观察到负超螺旋,从而证明了端粒拓扑约束的存在,但由于缺乏适当的工具,从未探测到正超螺旋。事实上,目前可用的少数工具只能研究未缠绕(三氧杂苯并)或过缠绕(GapR)的 DNA 拓扑结构(扭转变化),而不能探测扭曲的变化(超螺旋和纽结)。为了解决这个问题,我们设计了创新的工具,旨在分析细胞中正负 DNA 扭曲。使用这些工具,我们可以观察到复制应激后和端粒上拓扑异构酶 2 抑制后正超螺旋的积累。TRF2 耗竭导致端粒松弛和正超螺旋增加,而 TSA 抑制组蛋白去乙酰化酶 I 和 II 仅导致端粒松弛。在端粒之外,我们还观察到复制应激后 FRA3B 脆性位点上正超螺旋的积累,这表明该位点的 DNA 脆弱性具有拓扑模型。