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An epigenomic role of Fe65 in the cellular response to DNA damage.

ABSTRACT: In this study, we hypothesized that the transcriptional activity of Fe65 may contribute to DNA damage pathways by regulating gene expression patterns activated in response to genotoxic stress. To address this hypothesis, we mapped the global binding profile of Fe65 by chromatin immunoprecipitation (ChIP)-sequencing in the SK-N-SH cells exposed to genotoxic stress. Unexpectedly, the genome-wide location analysis showed a substantial enrichment of Fe65 in the promoter regions of coding genes linked to DNA damage signaling pathways.

ORGANISM(S): Homo sapiens

PROVIDER: GSE97149 | GEO | 2017/03/29

SECONDARY ACCESSION(S): PRJNA380811

REPOSITORIES: GEO

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