Skene Peter J, Henikoff Steven
Howard Hughes Medical Institute, Basic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, United States.
Elife. 2017 Jan 16;6:e21856. doi: 10.7554/eLife.21856.
We describe Cleavage Under Targets and Release Using Nuclease (CUT&RUN), a chromatin profiling strategy in which antibody-targeted controlled cleavage by micrococcal nuclease releases specific protein-DNA complexes into the supernatant for paired-end DNA sequencing. Unlike Chromatin Immunoprecipitation (ChIP), which fragments and solubilizes total chromatin, CUT&RUN is performed in situ, allowing for both quantitative high-resolution chromatin mapping and probing of the local chromatin environment. When applied to yeast and human nuclei, CUT&RUN yielded precise transcription factor profiles while avoiding crosslinking and solubilization issues. CUT&RUN is simple to perform and is inherently robust, with extremely low backgrounds requiring only ~1/10th the sequencing depth as ChIP, making CUT&RUN especially cost-effective for transcription factor and chromatin profiling. When used in conjunction with native ChIP-seq and applied to human CTCF, CUT&RUN mapped directional long range contact sites at high resolution. We conclude that in situ mapping of protein-DNA interactions by CUT&RUN is an attractive alternative to ChIP-seq.
我们描述了一种名为“靶向切割并利用核酸酶释放(CUT&RUN)”的染色质分析策略,该策略中,微球菌核酸酶通过抗体靶向控制切割,将特定的蛋白质-DNA复合物释放到上清液中,用于双端DNA测序。与染色质免疫沉淀(ChIP)不同,ChIP会使总染色质片段化并溶解,而CUT&RUN是原位进行的,既能实现定量高分辨率染色质图谱绘制,又能探究局部染色质环境。当应用于酵母和人类细胞核时,CUT&RUN产生了精确的转录因子图谱,同时避免了交联和溶解问题。CUT&RUN操作简单,本质上很稳健,背景极低,测序深度仅为ChIP的约十分之一,这使得CUT&RUN在转录因子和染色质分析方面极具成本效益。当与天然ChIP-seq结合使用并应用于人类CTCF时,CUT&RUN以高分辨率绘制了定向长程接触位点。我们得出结论,通过CUT&RUN对蛋白质-DNA相互作用进行原位图谱绘制是ChIP-seq的一种有吸引力的替代方法。