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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5310842/ https://www.ncbi.nlm.nih.gov/pubmed/28079019 http://dx.doi.org/10.7554/eLife.21856 |
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author | Skene, Peter J Henikoff, Steven |
author_facet | Skene, Peter J Henikoff, Steven |
author_sort | Skene, Peter J |
collection | PubMed |
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. DOI: http://dx.doi.org/10.7554/eLife.21856.001 |
format | Online Article Text |
id | pubmed-5310842 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-53108422017-02-17 An efficient targeted nuclease strategy for high-resolution mapping of DNA binding sites Skene, Peter J Henikoff, Steven eLife Genes and Chromosomes 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. DOI: http://dx.doi.org/10.7554/eLife.21856.001 eLife Sciences Publications, Ltd 2017-01-16 /pmc/articles/PMC5310842/ /pubmed/28079019 http://dx.doi.org/10.7554/eLife.21856 Text en © 2017, Skene et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Genes and Chromosomes Skene, Peter J Henikoff, Steven An efficient targeted nuclease strategy for high-resolution mapping of DNA binding sites |
title | 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_short | 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 |
topic | Genes and Chromosomes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5310842/ https://www.ncbi.nlm.nih.gov/pubmed/28079019 http://dx.doi.org/10.7554/eLife.21856 |
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