Martín-Parras L, Lucas I, Martínez-Robles M L, Hernández P, Krimer D B, Hyrien O, Schvartzman J B
Departamento de Biología Celular y del Desarrollo, CIB (CSIC), Velázquez 144, 28006 Madrid, Spain.
Nucleic Acids Res. 1998 Jul 15;26(14):3424-32. doi: 10.1093/nar/26.14.3424.
Neutral/neutral two-dimensional (2D) agarose gelelectrophoresis was used to investigate populations of the different topological conformations that pBR322 can adopt in vivo in bacterial cells as well as in Xenopus egg extracts. To help in interpretation and identification of all the different signals, undigested as well as DNA samples pretreated with DNase I, topoisomerase I and topoisomerase II were analyzed. The second dimension of the 2D gel system was run with or without ethidium bromide to account for any possible changes in the migration behavior of DNA molecules caused by intercalation of this planar agent. Finally, DNA samples were isolated from a recA-strain of Escherichia coli , as well as after direct labeling of the replication intermediates in extracts of Xenopus laevis eggs. Altogether, the results obtained demonstrated that 2D gels can be readily used to identify most of the complex topological populations that circular molecules can adopt in vivo in both bacteria and eukaryotic cells.
使用中性/中性二维(2D)琼脂糖凝胶电泳来研究pBR322在细菌细胞以及非洲爪蟾卵提取物中体内可采用的不同拓扑构象群体。为了有助于解释和识别所有不同的信号,分析了未消化的以及用DNase I、拓扑异构酶I和拓扑异构酶II预处理的DNA样品。二维凝胶系统的第二维在有或没有溴化乙锭的情况下进行电泳,以考虑这种平面试剂的嵌入对DNA分子迁移行为可能产生的任何变化。最后,从大肠杆菌的recA菌株中分离DNA样品,以及在直接标记非洲爪蟾卵提取物中的复制中间体之后进行分离。总之,所获得的结果表明,二维凝胶可很容易地用于识别环状分子在细菌和真核细胞体内可采用的大多数复杂拓扑群体。