TY - JOUR
T1 - Cistrome and Epicistrome Features Shape the Regulatory DNA Landscape
AU - O'Malley, Ronan C.
AU - Huang, Shao Shan Carol
AU - Song, Liang
AU - Lewsey, Mathew G.
AU - Bartlett, Anna
AU - Nery, Joseph R.
AU - Galli, Mary
AU - Gallavotti, Andrea
AU - Ecker, Joseph R.
N1 - Funding Information:
Betty Moore Foundation (GBMF3034)
Funding Information:
We thank Andrew Kuruzar for assistance with images ( p40design@gmail.com ). We thank Chris Benner, Ian Quigley, Debra Fulton, Robert Schmitz, and Yue Zhao for their critical reading of the manuscript. We thank Rosa Castanon for sharing biological materials. A.G. acknowledges funding from NSF (IOS-0820729/IOS-1114484). This work was supported by grants from the NSF (MCB1024999) and the Gordon and Betty Moore Foundation (GBMF3034) (to J.R.E.). J.R.E. is an Investigator of the Howard Hughes Medical Institute.
Publisher Copyright:
© 2016 Elsevier Inc.
PY - 2016/5/19
Y1 - 2016/5/19
N2 - 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.
AB - 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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U2 - 10.1016/j.cell.2016.04.038
DO - 10.1016/j.cell.2016.04.038
M3 - Article
C2 - 27203113
AN - SCOPUS:84975134214
SN - 0092-8674
VL - 165
SP - 1280
EP - 1292
JO - Cell
JF - Cell
IS - 5
ER -