Efficient isolation of specific genomic regions and identification of associated proteins by engineered DNA-binding molecule-mediated chromatin immunoprecipitation (enChIP) using CRISPR

被引:130
作者
Fujita, Toshitsugu [1 ]
Fujii, Hodaka [1 ]
机构
[1] Osaka Univ, Combined Program Microbiol & Immunol, Microbial Dis Res Inst, Suita, Osaka 5650871, Japan
关键词
enChIP; CRISPR; dCas9; gRNA; Mass spectrometry; Locus-specific biochemical epigenetics/chromatin biochemistry; ADAPTIVE IMMUNITY; RNA; GENES; PURIFICATION; BACTERIA;
D O I
10.1016/j.bbrc.2013.08.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Isolation of specific genomic regions retaining molecular interactions is necessary for their biochemical analysis. Here, we established a novel method, engineered DNA-binding molecule-mediated chromatin immunoprecipitation (enChIP), for purification of specific genomic regions retaining molecular interactions. We showed that enChIP using the CRISPR system efficiently isolates specific genomic regions. In this form of enChIP, specific genomic regions are immunoprecipitated with antibody against a tag(s), which is fused to a catalytically inactive form of Cas9 (dCas9), which is co-expressed with a guide RNA (gRNA) and recognizes endogenous DNA sequence in the genomic regions of interest. enChIP-mass spectrometry (enChIP-MS) targeting endogenous loci identified associated proteins. enChIP using the CRISPR system would be a convenient and useful tool for dissecting chromatin structure of genomic regions of interest. (C) 2013 The Authors. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:132 / 136
页数:5
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