High-resolution TADs reveal DNA sequences underlying genome organization in flies

被引:569
作者
Ramirez, Fidel [1 ]
Bhardwaj, Vivek [1 ,2 ]
Arrigoni, Laura [1 ]
Lam, Kin Chung [1 ]
Gruening, Bjoern A. [3 ]
Villaveces, Jose [4 ]
Habermann, Bianca [4 ]
Akhtar, Asifa [1 ]
Manke, Thomas [1 ]
机构
[1] Max Planck Inst Immunobiol & Epigenet, Stubeweg 51, D-79108 Freiburg, Germany
[2] Univ Freiburg, Fac Biol, Schanzlestr 1, D-79104 Freiburg, Germany
[3] Univ Freiburg, Dept Comp Sci, Georges Kohler Allee 106, D-79110 Freiburg, Germany
[4] Max Planck Inst Biochem & Computat Biol, Klopferspitz 18, D-82152 Martinsried, Germany
关键词
3D CHROMATIN ORGANIZATION; CHIP-SEQ DATA; TRANSCRIPTION FACTOR; DROSOPHILA GENOME; CHROMOSOME ORGANIZATION; ARCHITECTURAL PROTEINS; INSULATOR PROTEINS; GENE-REGULATION; BINDING SITES; GAGA-FACTOR;
D O I
10.1038/s41467-017-02525-w
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
Despite an abundance of new studies about topologically associating domains (TADs), the role of genetic information in TAD formation is still not fully understood. Here we use our software, HiCExplorer (hicexplorer. readthedocs. io) to annotate > 2800 high-resolution (570 bp) TAD boundaries in Drosophila melanogaster. We identify eight DNA motifs enriched at boundaries, including a motif bound by the M1BP protein, and two new boundary motifs. In contrast to mammals, the CTCF motif is only enriched on a small fraction of boundaries flanking inactive chromatin while most active boundaries contain the motifs bound by the M1BP or Beaf-32 proteins. We demonstrate that boundaries can be accurately predicted using only the motif sequences at open chromatin sites. We propose that DNA sequence guides the genome architecture by allocation of boundary proteins in the genome. Finally, we present an interactive online database to access and explore the spatial organization of fly, mouse and human genomes, available at http://chorogenome.ie-freiburg.mpg.de.
引用
收藏
页数:15
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