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Cistrome and Epicistrome Features Shape the Regulatory DNA Landscape
Author(s) -
Ronan C. O’Malley,
Shaoshan Carol Huang,
Liang Song,
Mathew G. Lewsey,
Anna Bartlett,
Joseph R. Nery,
Mary Galli,
Andrea Gallavotti,
Joseph R. Ecker
Publication year - 2016
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2016.04.038
Subject(s) - biology , arabidopsis , computational biology , dna methylation , transcription factor , dna binding site , epigenomics , dna , genetics , binding site , organism , genomics , genome , gene , promoter , gene expression , mutant
The cistrome is the complete set of transcription factor (TF) binding sites (cis-elements) in an organism, while an epicistrome incorporates tissue-specific DNA chemical modifications and TF-specific chemical sensitivities into these binding profiles. Robust methods to construct comprehensive cistrome and epicistrome maps are critical for elucidating complex transcriptional networks that underlie growth, behavior, and disease. Here, we describe DNA affinity purification sequencing (DAP-seq), a high-throughput TF binding site discovery method that interrogates genomic DNA with in-vitro-expressed TFs. Using DAP-seq, we defined the Arabidopsis cistrome by resolving motifs and peaks for 529 TFs. Because genomic DNA used in DAP-seq retains 5-methylcytosines, we determined that >75% (248/327) of Arabidopsis TFs surveyed were methylation sensitive, a property that strongly impacts the epicistrome landscape. DAP-seq datasets also yielded insight into the biology and binding site architecture of numerous TFs, demonstrating the value of DAP-seq for cost-effective cistromic and epicistromic annotation in any organism.

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