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| Status |
Public on Nov 22, 2017 |
| Title |
Sub-kb resolution Hi-C in D. melanogaster reveals conserved characteristics of TADs between insect and mammalian cells |
| Organism |
Drosophila melanogaster |
| Experiment type |
Expression profiling by high throughput sequencing
Other
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| Summary |
Topologically associating domains (TADs) are widely recognized as fundamental elements of the 3D structure of the eukaryotic genome. However, while the structural importance of the insulator protein CTCF together with cohesin at TAD borders in mammalian cells is well established, the absence of such co-localization at most TAD borders in recent Hi-C studies of D. melanogaster is enigmatic, raising the possibility that these TAD border elements are not generally conserved among metazoans. Using in situ Hi-C with sub-kb resolution, we show that the genome of D. melanogaster is almost completely partitioned into more than 4,000 TADs (median size, 13 kb), nearly 7-fold more than previously identified. The overwhelming majority of these TADs are demarcated by pairs of Drosophila-specific insulator proteins, BEAF-32/CP190 or BEAF-32/Chromator, indicating that these proteins may play an analogous role in Drosophila as that of the CTCF/cohesin pair in mammals. Moreover, we find that previously identified TADs enriched for inactive chromatin are predominantly assembled from the higher-level interactions between smaller TADs. In contrast, the closely-spaced small TADs in regions previously thought to be unstructured “inter-TADs” are organized in an open configuration with far fewer TAD-TAD interactions. Such structures can also be identified in some “inter-TAD” regions of the mammalian genome, suggesting that larger assemblages of small self-interacting TADs separated by a “burst” of adjacent small, weakly interacting TADs may be a conserved, basic characteristic of the higher order folding of the metazoan genome.
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| Overall design |
The genome-wide interactome with sub-kb resolution were generated using in-situ Hi-C method in both asychonous Drosophola cell line S2R+ and the cells that were arrest at G1/S
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| Contributor(s) |
Wang Q, Shao Z |
| Citation missing |
Has this study been published? Please login to update or notify GEO. |
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| Submission date |
Jul 12, 2017 |
| Last update date |
Apr 14, 2020 |
| Contact name |
Qi Wang |
| E-mail(s) |
rubbyqi@sjtu.edu.cn
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| Organization name |
Shanghai Jiaotong University
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| Street address |
800 Dong Chuan Rd.
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| City |
Shanghai |
| State/province |
Shanghai |
| ZIP/Postal code |
200240 |
| Country |
China |
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| Platforms (1) |
| GPL23702 |
HiSeq X Ten (Drosophila melanogaster) |
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| Samples (6)
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| Relations |
| BioProject |
PRJNA393992 |
| SRA |
SRP111713 |
| Supplementary file |
Size |
Download |
File type/resource |
| GSE101317_G1S_genes.txt.gz |
319.7 Kb |
(ftp)(http) |
TXT |
| GSE101317_S2Rplus_G1S_domain.txt.gz |
29.5 Kb |
(ftp)(http) |
TXT |
| GSE101317_combined_read_pairs.txt.gz |
1.9 Gb |
(ftp)(http) |
TXT |
SRA Run Selector |
| Raw data are available in SRA |
| Processed data are available on Series record |
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