John Sam, Sabo Peter J, Canfield Theresa K, Lee Kristen, Vong Shinny, Weaver Molly, Wang Hao, Vierstra Jeff, Reynolds Alex P, Thurman Robert E, Stamatoyannopoulos John A
Department of Genome Sciences, University of Washington, Seattle, Washington, USA.
Curr Protoc Mol Biol. 2013 Jul;Chapter 27:Unit 21.27. doi: 10.1002/0471142727.mb2127s103.
DNase I-seq is a global and high-resolution method that uses the nonspecific endonuclease DNase I to map chromatin accessibility. These accessible regions, designated as DNase I hypersensitive sites (DHSs), define the regulatory features, (e.g., promoters, enhancers, insulators, and locus control regions) of complex genomes. In this unit, methods are described for nuclei isolation, digestion of nuclei with limiting concentrations of DNase I, and the biochemical fractionation of DNase I hypersensitive sites in preparation for high-throughput sequencing. DNase I-seq is an unbiased and robust method that is not predicated on an a priori understanding of regulatory patterns or chromatin features.
DNase I测序是一种全面且高分辨率的方法,它利用非特异性核酸内切酶DNase I来绘制染色质可及性图谱。这些可及区域,即DNase I超敏位点(DHSs),定义了复杂基因组的调控特征(例如启动子、增强子、绝缘子和基因座控制区)。在本单元中,将介绍用于细胞核分离、用有限浓度的DNase I消化细胞核以及对DNase I超敏位点进行生化分级分离以准备高通量测序的方法。DNase I测序是一种无偏差且稳健的方法,它并不依赖于对调控模式或染色质特征的先验理解。