An efficient targeted nuclease strategy for high-resolution mapping of DNA binding sites

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 Immunoprecip...

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Main Authors: Peter J Skene, Steven Henikoff
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2017-01-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/21856
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spelling doaj-bb7be78a927f456284491ff163b499a72021-05-05T13:11:15ZengeLife Sciences Publications LtdeLife2050-084X2017-01-01610.7554/eLife.21856An efficient targeted nuclease strategy for high-resolution mapping of DNA binding sitesPeter J Skene0Steven Henikoff1https://orcid.org/0000-0002-7621-8685Howard Hughes Medical Institute, Basic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, United StatesHoward Hughes Medical Institute, Basic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, United StatesWe 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.https://elifesciences.org/articles/21856transcription factorschromatinin situ profilingDNA sequencing
collection DOAJ
language English
format Article
sources DOAJ
author Peter J Skene
Steven Henikoff
spellingShingle Peter J Skene
Steven Henikoff
An efficient targeted nuclease strategy for high-resolution mapping of DNA binding sites
eLife
transcription factors
chromatin
in situ profiling
DNA sequencing
author_facet Peter J Skene
Steven Henikoff
author_sort Peter J Skene
title An efficient targeted nuclease strategy for high-resolution mapping of DNA binding sites
title_short An efficient targeted nuclease strategy for high-resolution mapping of DNA binding sites
title_full An efficient targeted nuclease strategy for high-resolution mapping of DNA binding sites
title_fullStr An efficient targeted nuclease strategy for high-resolution mapping of DNA binding sites
title_full_unstemmed An efficient targeted nuclease strategy for high-resolution mapping of DNA binding sites
title_sort efficient targeted nuclease strategy for high-resolution mapping of dna binding sites
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2017-01-01
description 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.
topic transcription factors
chromatin
in situ profiling
DNA sequencing
url https://elifesciences.org/articles/21856
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