Regulatory analysis of the C. elegans genome with spatiotemporal resolution

被引:84
作者
Araya, Carlos L. [1 ]
Kawli, Trupti [1 ]
Kundaje, Anshul [2 ]
Jiang, Lixia [1 ]
Wu, Beijing [1 ]
Vafeados, Dionne [3 ]
Terrell, Robert [3 ]
Weissdepp, Peter [3 ]
Gevirtzman, Louis [3 ]
Mace, Daniel [3 ]
Niu, Wei [4 ]
Boyle, Alan P. [1 ]
Xie, Dan [1 ]
Ma, Lijia [5 ]
Murray, John I. [6 ]
Reinke, Valerie [4 ]
Waterston, Robert H. [3 ]
Snyder, Michael [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Genet, Stanford, CA 94305 USA
[2] MIT, Dept Comp Sci, Cambridge, MA 02139 USA
[3] Univ Washington, Dept Genome Sci, Seattle, WA 98195 USA
[4] Yale Univ, Sch Med, Dept Genet, New Haven, CT 06520 USA
[5] Univ Chicago, Inst Genom & Syst Biol, Chicago, IL 60637 USA
[6] Univ Penn, Perelman Sch Med, Dept Genet, Philadelphia, PA 19104 USA
关键词
CAENORHABDITIS-ELEGANS; GENE-EXPRESSION; CELL LINEAGE; CHIP-SEQ; TRANSCRIPTION FACTORS; FACTOR COLOCALIZATION; BINDING; MORPHOGENESIS; SIMILARITY; HOMOLOG;
D O I
10.1038/nature13497
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
Discovering the structure and dynamics of transcriptional regulatory events in the genome with cellular and temporal resolution is crucial to understanding the regulatory underpinnings of development and disease. We determined the genomic distribution of binding sites for 92 transcription factors and regulatory proteins across multiple stages of Caenorhabditis elegans development by performing 241 ChIP-seq (chromatin immunoprecipitation followed by sequencing) experiments. Integration of regulatory binding and cellular-resolution expression data produced a spatio-temporally resolved metazoan transcription factor binding map. Using this map, we explore developmental regulatory circuits that encode combinatorial logic at the levels of co-binding and co-expression of transcription factors, characterizing the genomic coverage and clustering of regulatory binding, the binding preferences of, and biological processes regulated by, transcription factors, the global transcription factor co-associations and genomic subdomains that suggest shared patterns of regulation, and identifying key transcription factors and transcription factor co-associations for fate specification of individual lineages and cell types.
引用
收藏
页码:400 / U363
页数:24
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