染色质
CTCF公司
染色质免疫沉淀
芯片排序
DNA
核酸酶
生物
芯片对芯片
计算生物学
转录因子
细胞生物学
分子生物学
微球菌核酸酶
遗传学
染色质重塑
核小体
基因
基因表达
发起人
增强子
作者
Peter J. Skene,Steven Henikoff
出处
期刊:eLife
[eLife Sciences Publications Ltd]
日期:2017-01-16
卷期号:6
被引量:1224
摘要
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.
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