Determination and inference of eukaryotic transcription factor sequence specificity.

Determination and inference of eukaryotic transcription factor sequence specificity.
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DOI:
10.1016/j.cell.2014.08.009
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发表时间:
2014-09-11
期刊:
影响因子:
64.5
通讯作者:
Hughes TR
Hughes TR
中科院分区:
生物学1区
文献类型:
--
作者:
Weirauch MT;Yang A;Albu M;Cote AG;Montenegro-Montero A;Drewe P;Najafabadi HS;Lambert SA;Mann I;Cook K;Zheng H;Goity A;van Bakel H;Lozano JC;Galli M;Lewsey MG;Huang E;Mukherjee T;Chen X;Reece-Hoyes JS;Govindarajan S;Shaulsky G;Walhout AJM;Bouget FY;Ratsch G;Larrondo LF;Ecker JR;Hughes TR

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Transcription factor (TF) DNA sequence preferences direct their regulatory activity, but are currently known for only ~1% of all eukaryotic TFs. Broadly sampling DNA-binding domain (DBD) types from multiple eukaryotic clades, we determined DNA sequence preferences for >1,000 TFs encompassing 54 different DBD classes from 131 diverse eukaryotes. We find that closely related DBDs almost always have very similar DNA sequence preferences, enabling inference of motifs for ~34% of the ~170,000 known or predicted eukaryotic TFs. Sequences matching both measured and inferred motifs are enriched in ChIP-seq peaks and upstream of transcription start sites in diverse eukaryotic lineages. SNPs defining expression quantitative trait loci in Arabidopsis promoters are also enriched for predicted TF binding sites. Importantly, our motif “library” (http://cisbp.ccbr.utoronto.ca) can be used to identify specific TFs whose binding may be altered by human disease risk alleles. These data present a powerful resource for mapping transcriptional networks across eukaryotes.
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