El Sayyed Hafez, Espéli Olivier
Center for Interdisciplinary Research in Biology (CIRB), College de France, CNRS/UMR 7241 - INSERM U1050, PSL Research University, 11, Place Marcelin Berthelot, Paris Cedex 05, 75231, France.
Methods Mol Biol. 2018;1703:87-94. doi: 10.1007/978-1-4939-7459-7_6.
This methods article described a protocol aiming at mapping E. coli Topoisomerase IV (Topo IV) binding and cleavage activity sites on the genome. The approach is readily applicable to any Type II topoisomerase on a broad variety of gram-positive and gram-negative bacterial species. Conventional ChIP-seq of flag tagged Topo IV subunits and a novel method aimed at trapping only DNA bound to active Topo IV (called NorfliP) are described. NorfliP relies on the ability of norfloxacin, a quinolone drug, to cross-link the 5' ends of the DNA breaks with the catalytic tyrosine of bacterial Type II topoisomerases. These methods give complementary results and their combination brought important insights on both the function and regulation of Topo IV.
这篇方法学文章描述了一种旨在绘制大肠杆菌拓扑异构酶IV(Topo IV)在基因组上的结合和切割活性位点的方案。该方法很容易应用于多种革兰氏阳性和革兰氏阴性细菌物种中的任何II型拓扑异构酶。文中描述了对带有Flag标签的Topo IV亚基进行的传统染色质免疫沉淀测序(ChIP-seq)以及一种旨在仅捕获与活性Topo IV结合的DNA的新方法(称为NorfliP)。NorfliP依赖于喹诺酮类药物诺氟沙星将DNA断裂的5'末端与细菌II型拓扑异构酶的催化酪氨酸交联的能力。这些方法给出了互补的结果,它们的结合为Topo IV的功能和调控带来了重要的见解。