Combinatorial binding predicts spatio-temporal cis-regulatory activity

被引:307
作者
Zinzen, Robert P. [1 ]
Girardot, Charles [1 ]
Gagneur, Julien [1 ]
Braun, Martina [1 ]
Furlong, Eileen E. M. [1 ]
机构
[1] European Mol Biol Lab, D-69117 Heidelberg, Germany
关键词
TRANSCRIPTION FACTOR-BINDING; MUSCLE-CELL LINEAGES; GENOME-WIDE ANALYSIS; MESODERM DEVELOPMENT; GENE MEF2; DROSOPHILA; INTEGRATION; ELEMENTS; TINMAN; TWIST;
D O I
10.1038/nature08531
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Development requires the establishment of precise patterns of gene expression, which are primarily controlled by transcription factors binding to cis-regulatory modules. Although transcription factor occupancy can now be identified at genome-wide scales, decoding this regulatory landscape remains a daunting challenge. Here we used a novel approach to predict spatio-temporal cis-regulatory activity based only on in vivo transcription factor binding and enhancer activity data. We generated a high-resolution atlas of cis-regulatory modules describing their temporal and combinatorial occupancy during Drosophila mesoderm development. The binding profiles of cis-regulatory modules with characterized expression were used to train support vector machines to predict five spatio-temporal expression patterns. In vivo transgenic reporter assays demonstrate the high accuracy of these predictions and reveal an unanticipated plasticity in transcription factor binding leading to similar expression. This data-driven approach does not require previous knowledge of transcription factor sequence affinity, function or expression, making it widely applicable.
引用
收藏
页码:65 / U72
页数:8
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