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10.1016/j.cell.2016.04.038

http://scihub22266oqcxt.onion/10.1016/j.cell.2016.04.038
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C4907330!4907330!27203113
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suck abstract from ncbi


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pmid27203113      Cell 2016 ; 165 (5): 1280-92
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  • Cistrome and Epicistrome Features Shape the Regulatory DNA Landscape #MMPMID27203113
  • O?Malley RC; Huang SsC; Song L; Lewsey MG; Bartlett A; Nery JR; Galli M; Gallavotti A; Ecker JR
  • Cell 2016[May]; 165 (5): 1280-92 PMID27203113show ga
  • 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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