An efficient targeted nuclease strategy for high-resolution mapping of DNA binding sites.
Peter J SkeneSteven HenikoffPublished in: eLife (2017)
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.
Keyphrases
- transcription factor
- high resolution
- dna binding
- genome wide
- single cell
- circulating tumor
- dna damage
- cell free
- gene expression
- single molecule
- circulating tumor cells
- high throughput
- endothelial cells
- mass spectrometry
- rna seq
- dna methylation
- high speed
- tandem mass spectrometry
- cancer therapy
- protein protein
- amino acid
- optical coherence tomography
- liquid chromatography