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Active Promoters give rise to false positive 'Phantom Peaks' in ChIP-Seq experiments


ABSTRACT: We applied ChIP-seq to map the chromosomal binding sites for two nucleosome remodeling complexes containing the ATPase ISWI, ACF and RSF, in Drosophila embryos. Employing a panel of polyclonal and monoclonal antibodies directed against their signature subunits, ACF1 and RSF1, robust profiles were obtained indicating that both remodelers co-occupied a large set of active promoters. For further validation we repeated the mapping using chromatin of mutant embryos that do not express ACF1 or RSF1. Surprisingly, the ChIP-seq profiles were unchanged, suggesting that they were not due to specific immunoprecipitation. Conservative analysis lists about 3000 chromosomal loci, mostly active promoters that are prone to non-specific enrichment in ChIP and give rise to ‘Phantom Peaks’. These peaks are not obtained with pre-immune serum and are not prominent in input chromatin. Examination of various ACF1 and RSF1 antibodies in Drosophila melanogaster embryos which are wildtype or mutant for the antibody targets.

ORGANISM(S): Drosophila melanogaster

SUBMITTER: Tobias Straub 

PROVIDER: E-GEOD-67323 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Active promoters give rise to false positive 'Phantom Peaks' in ChIP-seq experiments.

Jain Dhawal D   Baldi Sandro S   Zabel Angelika A   Straub Tobias T   Becker Peter B PB  

Nucleic acids research 20150627 14


Chromatin immunoprecipitation (ChIP) is widely used to identify chromosomal binding sites. Chromatin proteins are cross-linked to their target sequences in living cells. The purified chromatin is sheared and the relevant protein is enriched by immunoprecipitation with specific antibodies. The co-purifying genomic DNA is then determined by massive parallel sequencing (ChIP-seq).We applied ChIP-seq to map the chromosomal binding sites for two ISWI-containing nucleosome remodeling factors, ACF and  ...[more]

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