Zawadzki Pawel, Stracy Mathew, Ginda Katarzyna, Zawadzka Katarzyna, Lesterlin Christian, Kapanidis Achillefs N, Sherratt David J
Department of Biochemistry, University of Oxford, South Parks Road, Oxford OX1 3QU, UK.
Biological Physics Research Group, Clarendon Laboratory, Department of Physics, University of Oxford, Parks Road, Oxford OX1 3PU, UK.
Cell Rep. 2015 Dec 22;13(11):2587-2596. doi: 10.1016/j.celrep.2015.11.034. Epub 2015 Dec 10.
The type II topoisomerase TopoIV, which has an essential role in Escherichia coli chromosome decatenation, interacts with MukBEF, an SMC (structural maintenance of chromosomes) complex that acts in chromosome segregation. We have characterized the intracellular dynamics of individual TopoIV molecules and the consequences of their interaction with MukBEF clusters by using photoactivated-localization microscopy. We show that ~15 TopoIV molecules per cell are associated with MukBEF clusters that are preferentially localized to the replication origin region (ori), close to the long axis of the cell. A replication-dependent increase in the fraction of immobile molecules, together with a proposed catalytic cycle of ~1.8 s, is consistent with the majority of active TopoIV molecules catalyzing decatenation, with a minority maintaining steady-state DNA supercoiling. Finally, we show that the MukB-ParC interaction is crucial for timely decatenation and segregation of newly replicated ori DNA.
II型拓扑异构酶TopoIV在大肠杆菌染色体解连环过程中起关键作用,它与MukBEF相互作用,MukBEF是一种参与染色体分离的SMC(染色体结构维持)复合体。我们通过使用光激活定位显微镜,对单个TopoIV分子的细胞内动力学及其与MukBEF簇相互作用的后果进行了表征。我们发现,每个细胞中约有15个TopoIV分子与MukBEF簇相关联,这些簇优先定位于复制起始区域(ori),靠近细胞的长轴。与约1.8秒的推测催化循环一起,固定分子比例的复制依赖性增加与大多数活性TopoIV分子催化解连环一致,少数分子维持稳态DNA超螺旋。最后,我们表明MukB-ParC相互作用对于新复制的ori DNA的及时解连环和分离至关重要。