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Targeted in situ genome-wide profiling with high efficiency for low cell numbers
Author(s) -
Peter J. Skene,
Jorja G. Henikoff,
Steven Henikoff
Publication year - 2018
Publication title -
nature protocols
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.471
H-Index - 245
eISSN - 1754-2189
pISSN - 1750-2799
DOI - 10.1038/nprot.2018.015
Subject(s) - micrococcal nuclease , chromatin , nuclease , dna , histone , chromatin immunoprecipitation , biology , epigenomics , computational biology , microbiology and biotechnology , genetics , nucleosome , gene , dna methylation , gene expression , promoter
Cleavage under targets and release using nuclease (CUT&RUN) is an epigenomic profiling strategy in which antibody-targeted controlled cleavage by micrococcal nuclease releases specific protein-DNA complexes into the supernatant for paired-end DNA sequencing. As only the targeted fragments enter into solution, and the vast majority of DNA is left behind, CUT&RUN has exceptionally low background levels. CUT&RUN outperforms the most widely used chromatin immunoprecipitation (ChIP) protocols in resolution, signal-to-noise ratio and depth of sequencing required. In contrast to ChIP, CUT&RUN is free of solubility and DNA accessibility artifacts and has been used to profile insoluble chromatin and to detect long-range 3D contacts without cross-linking. Here, we present an improved CUT&RUN protocol that does not require isolation of nuclei and provides high-quality data when starting with only 100 cells for a histone modification and 1,000 cells for a transcription factor. From cells to purified DNA, CUT&RUN requires less than a day at the laboratory bench and requires no specialized skills.

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