生物
拟南芥
计算生物学
DNA甲基化
转录因子
DNA结合位点
表观遗传学
DNA
遗传学
结合位点
有机体
基因组学
基因
基因组
发起人
基因表达
突变体
作者
Ronan C. O’Malley,Shao‐shan Carol Huang,Liang Song,Mathew G. Lewsey,Anna Bartlett,Joseph R. Nery,Mary Galli,Andrea Gallavotti,Joseph R. Ecker
出处
期刊:Cell
[Cell Press]
日期:2016-05-01
卷期号:165 (5): 1280-1292
被引量:1420
标识
DOI:10.1016/j.cell.2016.04.038
摘要
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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