Kouzine Fedor, Baranello Laura, Levens David
Laboratory of Pathology, NCI/NIH, Bldg. 10, RM 2N105, Bethesda, MD, 20892, USA.
Laboratory of Pathology, NCI/NIH, Bethesda, MD, 20892, USA.
Methods Mol Biol. 2018;1703:95-108. doi: 10.1007/978-1-4939-7459-7_7.
Proteins manipulating intracellular DNA necessarily impart torsional stress, which redistributes across the DNA. Overtwisting and undertwisting of the double helix result in the manifestation of positive and negative DNA supercoiling. A growing body of evidence indicates that DNA topology is an important player in the key regulatory steps of genome function, highlighting the need for biochemical techniques to detect dynamic changes in the DNA structure. Psoralen binding to DNA in vivo is proportional to the level of supercoiling, providing an excellent probe for the topological state of nuclear DNA. Here we describe a psoralen-based methodology to detect transcription-induced DNA supercoiling genome-wide. The DNA samples generated with this approach can be hybridized to microarray platforms or high-throughput sequenced to provide a topological snapshot of the whole genome.
操控细胞内DNA的蛋白质必然会施加扭转应力,该应力会在DNA上重新分布。双螺旋的过度扭曲和扭曲不足会导致正、负DNA超螺旋的出现。越来越多的证据表明,DNA拓扑结构在基因组功能的关键调控步骤中起着重要作用,这凸显了需要生化技术来检测DNA结构的动态变化。补骨脂素在体内与DNA的结合与超螺旋水平成正比,为核DNA的拓扑状态提供了一个极佳的探针。在此,我们描述了一种基于补骨脂素的方法,用于全基因组范围内检测转录诱导的DNA超螺旋。用这种方法生成的DNA样本可与微阵列平台杂交或进行高通量测序,以提供全基因组的拓扑快照。