A cis-regulatory map of the Drosophila genome

被引:397
作者
Negre, Nicolas [1 ]
Brown, Christopher D. [1 ]
Ma, Lijia [1 ]
Bristow, Christopher Aaron [2 ]
Miller, Steven W. [3 ]
Wagner, Ulrich [4 ]
Kheradpour, Pouya [2 ]
Eaton, Matthew L. [5 ]
Loriaux, Paul [6 ]
Sealfon, Rachel [2 ]
Li, Zirong [4 ]
Ishii, Haruhiko [3 ]
Spokony, Rebecca F. [1 ]
Chen, Jia [7 ]
Hwang, Lindsay [4 ]
Cheng, Chao [8 ,9 ,10 ]
Auburn, Richard P. [11 ,12 ]
Davis, Melissa B. [1 ]
Domanus, Marc [1 ]
Shah, Parantu K. [13 ]
Morrison, Carolyn A. [1 ]
Zieba, Jennifer [1 ]
Suchy, Sarah [1 ]
Senderowicz, Lionel [1 ]
Victorsen, Alec [1 ]
Bild, Nicholas A. [1 ]
Grundstad, A. Jason [1 ]
Hanley, David [7 ]
MacAlpine, David M.
Mannervik, Mattias [14 ]
Venken, Koen [15 ]
Bellen, Hugo [15 ]
White, Robert [16 ]
Gerstein, Mark [8 ,9 ]
Russell, Steven [11 ,12 ]
Grossman, Robert L. [1 ,7 ,17 ]
Ren, Bing [4 ,18 ,19 ]
Posakony, James W. [3 ]
Kellis, Manolis [2 ]
White, Kevin P. [1 ]
机构
[1] Univ Chicago, Inst Genom & Syst Biol, Dept Human Genet, Chicago, IL 60637 USA
[2] MIT, Comp Sci & Artificial Intelligence Lab, Broad Inst MIT & Harvard, Cambridge, MA 02139 USA
[3] Univ Calif San Diego, Div Biol Sci CDB, La Jolla, CA 92093 USA
[4] Ludwig Inst Canc Res, La Jolla, CA 92093 USA
[5] Duke Univ, Dept Pharmacol & Canc Biol, Med Ctr, Durham, NC 27710 USA
[6] Univ Calif San Diego, Signaling Syst Lab, Dept Chem & Biochem, La Jolla, CA 92093 USA
[7] Univ Illinois, Natl Ctr Data Min, Chicago, IL 60607 USA
[8] Yale Univ, Program Computat Biol & Bioinformat, New Haven, CT 06520 USA
[9] Yale Univ, Dept Mol Biophys & Biochem, New Haven, CT 06520 USA
[10] Yale Univ, Dept Comp Sci, New Haven, CT 06520 USA
[11] Univ Cambridge, Dept Genet, Cambridge CB2 3EH, England
[12] Univ Cambridge, Cambridge Syst Biol Ctr, Cambridge CB2 3EH, England
[13] Harvard Univ, Sch Publ Hlth, Dana Farber Canc Inst, Dept Biostat & Computat Biol, Boston, MA 02115 USA
[14] Stockholm Univ, Dept Dev Biol, Wenner Gren Inst, Arrhenius Labs E3, S-10691 Stockholm, Sweden
[15] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA
[16] Univ Cambridge, Dept Physiol Dev & Neurosci, Cambridge CB2 3DY, England
[17] Univ Chicago, Dept Med, Chicago, IL 60637 USA
[18] Inst Genom Med, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
[19] Moores Canc Ctr, La Jolla, CA 92093 USA
关键词
TRANSCRIPTION FACTOR; ENHANCERS; MELANOGASTER; EXPRESSION; BLASTODERM; PROTEINS;
D O I
10.1038/nature09990
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
Systematic annotation of gene regulatory elements is a major challenge in genome science. Direct mapping of chromatin modification marks and transcriptional factor binding sites genome-wide(1,2) has successfully identified specific subtypes of regulatory elements(3). In Drosophila several pioneering studies have provided genome-wide identification of Polycomb response elements(4), chromatin states(5), transcription factor binding sites(6-9), RNA polymerase II regulation(8) and insulator elements(10); however, comprehensive annotation of the regulatory genome remains a significant challenge. Here we describe results from the modENCODE cis-regulatory annotation project. We produced a map of the Drosophila melanogaster regulatory genome on the basis of more than 300 chromatin immunoprecipitation data sets for eight chromatin features, five histone deacetylases and thirty-eight site-specific transcription factors at different stages of development. Using these data we inferred more than 20,000 candidate regulatory elements and validated a subset of predictions for promoters, enhancers and insulators in vivo. We identified also nearly 2,000 genomic regions of dense transcription factor binding associated with chromatin activity and accessibility. We discovered hundreds of new transcription factor co-binding relationships and defined a transcription factor network with over 800 potential regulatory relationships.
引用
收藏
页码:527 / 531
页数:5
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