| Literature DB >> 21870262 |
Abstract
Poly(ADP-ribose) polymerase1 (PARP1) is a global regulator of different cellular mechanisms, ranging from DNA damage repair to control of gene expression. Since PARP1 protein and pADPr have been shown to persist in chromatin through cell cycle, they may both act as epigenetic markers. However, it is not known how many loci are occupied by PARP1 protein during mitosis genome-wide. To reveal the genome-wide PARP1 binding sites, we used the ChIP-seq approach, an emerging technique to study genome-wide PARP1 protein interaction with chromatin. Here, we describe how to perform ChIP-seq in the context of PARP1 binding sites identification in chromatin, using human embryonic kidney cell lines.Entities:
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Year: 2011 PMID: 21870262 PMCID: PMC3164790 DOI: 10.1007/978-1-61779-270-0_12
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745