eLife · 2017 · 1.9K citations · 54 references
Life SciencesCell BiologyMolecular BiologyChromatin BiologyChromatin StructureGenomicsChromatinChromatin InteractionsDna SequencingLong-range Chromatin InteractionsCtcf Binding SitesMicrococcal Nuclease SequencingPaired-end SequencingProtein-dna Interactions
Unlike Chromatin Immunoprecipitation (ChIP), which fragments and solubilizes total chromatin, CUT&RUN is performed in situ, enabling quantitative high‑resolution chromatin mapping and probing of the local chromatin environment. The authors present CUT&RUN, a chromatin profiling strategy that uses antibody‑targeted micrococcal nuclease cleavage to release protein‑DNA complexes for sequencing. CUT&RUN achieves this by antibody‑targeted controlled cleavage with micrococcal nuclease, releasing the complexes into the supernatant for paired‑end DNA sequencing. Applied to yeast and human nuclei, CUT&RUN yielded precise transcription factor profiles without crosslinking or solubilization issues, proved simple and robust with extremely low background requiring only ~1/10th the sequencing depth of ChIP, and when combined with native ChIP‑seq mapped directional long‑range CTCF contact sites at high resolution, establishing it as a cost‑effective alternative to ChIP‑seq.
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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CTCF-Mediated Human 3D Genome Architecture Reveals Chromatin Topology for Transcription
Zhonghui Tang, Oscar Junhong Luo, Xingwang Li et al. · Cell · 2015 · 1.1K citations · Full text