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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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 |
work_keys_str_mv |
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