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Two independent modes of chromatin organization revealed by cohesin removal
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Abstract
Imaging and chromosome conformation capture studies have revealed several layers of chromosome organization, including segregation into megabase-sized active and inactive compartments, and partitioning into sub-megabase domains (TADs). It remains unclear, however, how these layers of organization form, interact with one another and influence genome function. Here we show that deletion of the cohesin-loading factor Nipbl in mouse liver leads to a marked reorganization of chromosomal folding. TADs and associated Hi-C peaks vanish globally, even in the absence of transcriptional changes. By contrast, compartmental segregation is preserved and even reinforced. Strikingly, the disappearance of TADs unmasks a finer compartment structure that accurately reflects the underlying epigenetic landscape. These observations demonstrate that the three-dimensional organization of the genome results from the interplay of two independent mechanisms: cohesin-independent segregation of the genome into fine-scale compartments, defined by chromatin state; and cohesin-dependent formation of TADs, possibly by loop extrusion, which helps to guide distant enhancers to their target genes.
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“Surprisingly however, deletion or degradation of cohesin or CTCF in differentiated cells has only mild effects on gene expression [344–349].”
From Transcriptional enhancers and their communication with gene promoters (2021) · cites this paper as [348]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“The A/B compartment structure does not disappear (and is in fact even strengthened) upon cohesin/CTCF depletion [344, 346–348], but, like TADs, dissolves in mitosis [459].”
From Transcriptional enhancers and their communication with gene promoters (2021) · cites this paper as [348]
Experimental — accuracy not yet measuredIn the citing paper
“complementary polymer simulation studies and Hi-C studies employing acute depletion of CTCF and cohesin, which also support such a dynamic model.”
From Recent evidence that TADs and chromatin loops are dynamic structures (2018) · cites this paper as [11]
In the citing paper
“Since multiple studies show that TADs and chromatin loops disappear without CTCF10,14 and cohesin,11,13–15 we reasoned that the most stable protein of CTCF and cohesin should set an upper limit on the stability of TADs and chromatin loops.”
From Recent evidence that TADs and chromatin loops are dynamic structures (2018) · cites this paper as [11]
In the citing paper
“In contrast, cohesin loss leads to disappearance of TADs because extrusion no longer takes place.11,13–15”
From Recent evidence that TADs and chromatin loops are dynamic structures (2018) · cites this paper as [11]
In the citing paper
“although CTCF and cohesin both appear absolutely required for the formation of most TADs10-15”
From Recent evidence that TADs and chromatin loops are dynamic structures (2018) · cites this paper as [11]
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Cites
Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2
Love, M. I., Huber, W., & Anders, S. (2014) · Genome Biology · doi:10.1186/s13059-014-0550-8 · Cited by 95,106
Self-citationSTAR: ultrafast universal RNA-seq aligner
Dobin, A., Davis, C. A., Schlesinger, F., Drenkow, J., Zaleski, C., Jha, S., Batut, P., Chaisson, M., & Gingeras, T. R. (2013) · Bioinformatics · doi:10.1093/bioinformatics/bts635 · Cited by 51,709
HISAT: a fast spliced aligner with low memory requirements
Kim, D., Langmead, B., & Salzberg, S. L. (2015) · Nature Methods · doi:10.1038/nmeth.3317 · Cited by 24,112
HTSeq—a Python framework to work with high-throughput sequencing data
Anders, S., Pyl, P. T., & Huber, W. (2015) · Bioinformatics · doi:10.1093/bioinformatics/btu638 · Cited by 21,464
Self-citationCommunity structure in social and biological networks
Girvan, M., & Newman, M. E. J. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.122653799 · Cited by 15,502
A 3D Map of the Human Genome at Kilobase Resolution Reveals Principles of Chromatin Looping
Rao, S. S. P., Huntley, M. H., Durand, N. C., Stamenova, E. K., Bochkov, I. D., Robinson, J. T., Sanborn, A. L., Machol, I., Omer, A. D., Lander, E. S., et al. (2014) · Cell · doi:10.1016/j.cell.2014.11.021 · Cited by 9,212
Comprehensive Mapping of Long-Range Interactions Reveals Folding Principles of the Human Genome
Lieberman-Aiden, E., van Berkum, N. L., Williams, L., Imakaev, M., Ragoczy, T., Telling, A., Amit, I., Lajoie, B. R., Sabo, P. J., Dorschner, M. O., et al. (2009) · Science · doi:10.1126/science.1181369 · Cited by 8,898
Self-citationTopological domains in mammalian genomes identified by analysis of chromatin interactions
Dixon, J. R., Selvaraj, S., Yue, F., Kim, A., Li, Y., Shen, Y., Hu, M., Liu, J. S., & Ren, B. (2012) · Nature · doi:10.1038/nature11082 · Cited by 6,829
GENCODE: The reference human genome annotation for The ENCODE Project
Harrow, J., Frankish, A., Gonzalez, J. M., Tapanari, E., Diekhans, M., Kokocinski, F., Aken, B. L., Barrell, D., Zadissa, A., Searle, S., et al. (2012) · Genome Research · doi:10.1101/gr.135350.111 · Cited by 4,585
Mapping and analysis of chromatin state dynamics in nine human cell types
Ernst, J., Kheradpour, P., Mikkelsen, T. S., Shoresh, N., Ward, L. D., Epstein, C. B., Zhang, X., Wang, L., Issner, R., Coyne, M., et al. (2011) · Nature · doi:10.1038/nature09906 · Cited by 2,898
Flagged first, then by citations
Research works printed but not linked: 2
- Wutz, G. et al. CTCF, WAPL and PDS5 proteins control the formation of TADs and loops by cohesin. Preprint at https://www.biorxiv.org/content/early/2017/08/18/177444 (2017) · DOI
- Bishop, C. M. Pattern Recognition and Machine Learning (Springer, 2006)
Cited by
Sorted by citations
Items 101–200 of 998
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Editing the Epigenome: Reshaping the Genomic Landscape
Holtzman, L., & Gersbach, C. A. (2018) · Annual Review of Genomics and Human Genetics · doi:10.1146/annurev-genom-083117-021632 · Cited by 147
Diverse silent chromatin states modulate genome compartmentalization and loop extrusion barriers
Spracklin, G., Abdennur, N. A., Imakaev, M., Chowdhury, N., Pradhan, S., Mirny, L. A., & Dekker, J. (2022) · Nature Structural & Molecular Biology · doi:10.1038/s41594-022-00892-7 · Cited by 144
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Self-citationWapl repression by Pax5 promotes V gene recombination by Igh loop extrusion
Hill, L., Ebert, A., Jaritz, M., Wutz, G., Nagasaka, K., Tagoh, H., Kostanova‐Poliakova, D., Schindler, K., Sun, Q., Bönelt, P., et al. (2020) · Nature · doi:10.1038/s41586-020-2454-y · Cited by 143
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Fudenberg, G., & Imakaev, M. (2017) · Nature Methods · doi:10.1038/nmeth.4329 · Cited by 141
Self-citationLiquid chromatin Hi-C characterizes compartment-dependent chromatin interaction dynamics
Belaghzal, H., Borrman, T. M., Stephens, A. D., Lafontaine, D. L. J., Venev, S. V., Weng, Z., Marko, J. F., & Dekker, J. (2021) · Nature Genetics · doi:10.1038/s41588-021-00784-4 · Cited by 136
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Arzate‐Mejía, R. G., Targa, F. R., & Corces, V. G. (2018) · Development · doi:10.1242/dev.137729 · Cited by 144
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Doğan, E. S., & Liu, C. (2018) · Nature Plants · doi:10.1038/s41477-018-0199-5 · Cited by 147
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Williamson, I., Kane, L., Devenney, P. S., Flyamer, I. M., Anderson, E., Kilanowski, F. M., Hill, R. E., Bickmore, W. A., & Lettice, L. A. (2019) · Development · doi:10.1242/dev.179523 · Cited by 148
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Luppino, J. M., Park, D. S., Nguyen, S. C., Lan, Y., Xu, Z., Yunker, R., & Joyce, E. F. (2020) · Nature Genetics · doi:10.1038/s41588-020-0647-9 · Cited by 122
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Chakraborty, S., Kopitchinski, N., Zuo, Z., Eraso, A., Awasthi, P., Chari, R., Mitra, A., Tobias, I. C., Moorthy, S. D., Dale, R. K., et al. (2023) · Nature Genetics · doi:10.1038/s41588-022-01295-6 · Cited by 120
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Mitter, M., Gasser, C., Takács, Z., Langer, C. C. H., Tang, W., Jessberger, G., Beales, C. T., Neuner, E., Ameres, S. L., Peters, J., et al. (2020) · Nature · doi:10.1038/s41586-020-2744-4 · Cited by 111
Self-citationCTCF and R-loops are boundaries of cohesin-mediated DNA looping
Zhang, H., Shi, Z., Banigan, E. J., Kim, Y., Yu, H., Bai, X., & Finkelstein, I. J. (2023) · Molecular Cell · doi:10.1016/j.molcel.2023.07.006 · Cited by 123
Emerging themes in cohesin cancer biology
Waldman, T. A. (2020) · Nature reviews. Cancer · doi:10.1038/s41568-020-0270-1 · Cited by 117
Liu, Y., Nanni, L., Sungalee, S., Zufferey, M., Tavernari, D., Mina, M., Ceri, S., Oricchio, E., & Ciriello, G. (2021) · Nature Communications · doi:10.1038/s41467-021-22666-3 · Cited by 112
Cohesin residency determines chromatin loop patterns
Costantino, L., Hsieh, T.-H. S., Lamothe, R. C., Darzacq, X., & Koshland, D. E. (2020) · eLife · doi:10.7554/elife.59889 · Cited by 125
The role of chromatin loop extrusion in antibody diversification
Zhang, Y., Zhang, X., Dai, H., Hu, H., & Alt, F. W. (2022) · Nature reviews. Immunology · doi:10.1038/s41577-022-00679-3 · Cited by 106
Barrington, C., Georgopoulou, D., Pezic, D., Varsally, W., Herrero, J., & Hadjur, S. (2019) · Nature Communications · doi:10.1038/s41467-019-10725-9 · Cited by 102
Laugsch, M., Bartusel, M., Rehimi, R., Alirzayeva, H., Karaolidou, A., Crispatzu, G., Zentis, P., Nikolić, M., Bleckwehl, T., Kolovos, P., et al. (2019) · Cell stem cell · doi:10.1016/j.stem.2019.03.004 · Cited by 106
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Zhang, S., Übelmesser, N., Josipović, N., Forte, G., Slotman, J. A., Chiang, M., Gothe, H. J., Gusmao, E. G., Becker, C., Altmüller, J., et al. (2021) · Science Advances · doi:10.1126/sciadv.abg8205 · Cited by 114
Račko, D., Benedetti, F., Dorier, J., & Stasiak, A. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkx1123 · Cited by 120
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Neguembor, M. V., Martin, L., Castells-García, Á., Gómez-García, P. A., Vicario, C., Carnevali, D., Abed, J. A., Granados, A., Sebastián-Pérez, R., Sottile, F., et al. (2021) · Molecular Cell · doi:10.1016/j.molcel.2021.06.009 · Cited by 106
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Surdez, D., Zaïdi, S., Grossetête, S., Laud-Duval, K., Ferre, A. S., Mous, L., Vourc’h, T., Tirode, F., Pierron, G., Raynal, V., et al. (2021) · Cancer Cell · doi:10.1016/j.ccell.2021.04.001 · Cited by 106
Crispatzu, G., Rehimi, R., Pachano, T., Bleckwehl, T., Cruz-Molina, S., Xiao, C., Mahabir, E., Bazzi, H., & Rada-Iglesias, A. (2021) · Nature Communications · doi:10.1038/s41467-021-24641-4 · Cited by 97
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Lin, X., Qi, Y., Latham, A. P., & Zhang, B. (2021) · The Journal of Chemical Physics · doi:10.1063/5.0044150 · Cited by 93
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Yokoshi, M., Kazuma, S., & Fukaya, T. (2020) · Molecular Cell · doi:10.1016/j.molcel.2020.02.007 · Cited by 89
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de Wit, E., & Nora, E. P. (2022) · Nature Reviews Genetics · doi:10.1038/s41576-022-00530-4 · Cited by 91
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Wang, R.-Y., Lee, J.-H., Kim, J., Xiong, F., Hasani, L. A., Shi, Y., Simpson, E. N., Zhu, X., Chen, Y.-T., Shivshankar, P., et al. (2023) · Nature Microbiology · doi:10.1038/s41564-023-01344-8 · Cited by 61
Conte, M., Irani, E., Chiariello, A. M., Abraham, A., Bianco, S., Esposito, A., & Nicodemi, M. (2022) · Nature Communications · doi:10.1038/s41467-022-31856-6 · Cited by 98
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van Ruiten, M. S., & Rowland, B. D. (2018) · Trends in Genetics · doi:10.1016/j.tig.2018.03.003 · Cited by 86
Visualizing the genome in high resolution challenges our textbook understanding
Lakadamyali, M., & Cosma, M. P. (2020) · Nature Methods · doi:10.1038/s41592-020-0758-3 · Cited by 92
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Chang, L., Ghosh, S., & Noordermeer, D. (2019) · Journal of Molecular Biology · doi:10.1016/j.jmb.2019.11.025 · Cited by 97
Tóthová, Z., Valton, A.-L., Gorelov, R. A., Vallurupalli, M., Krill-Burger, J. M., Holmes, A. L., Landers, C. C., Haydu, J. E., Małolepsza, E., Hartigan, C. R., et al. (2020) · JCI Insight · doi:10.1172/jci.insight.142149 · Cited by 90
BRD4 orchestrates genome folding to promote neural crest differentiation
Linares-Saldana, R., Kim, W., Bolar, N. A., Zhang, H., Koch-Bojalad, B. A., Yoon, S., Shah, P. P., Karnay, A. M., Park, D. S., Luppino, J. M., et al. (2021) · Nature Genetics · doi:10.1038/s41588-021-00934-8 · Cited by 91
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Hug, C. B., & Vaquerizas, J. M. (2018) · Trends in Genetics · doi:10.1016/j.tig.2018.09.002 · Cited by 90
Computational methods for analysing multiscale 3D genome organization
Zhang, Y., Boninsegna, L., Yang, M., Misteli, T., Alber, F., & Ma, J. (2023) · Nature Reviews Genetics · doi:10.1038/s41576-023-00638-1 · Cited by 97
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Wang, C., Colognori, D., Sunwoo, H., Wang, D., & Lee, J. T. (2019) · Nature Communications · doi:10.1038/s41467-019-10755-3 · Cited by 84
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Cajigas, I., Chakraborty, A., Swyter, K. R., Luo, H., Bastidas, M., Nigro, M., Morris, E. R., Chen, S., VanGompel, M. J. W., Leib, D., et al. (2018) · Molecular Cell · doi:10.1016/j.molcel.2018.07.024 · Cited by 82
Forces driving the three‐dimensional folding of eukaryotic genomes
Rada-Iglesias, Á., Grosveld, F. G., & Papantonis, A. (2018) · Molecular Systems Biology · doi:10.15252/msb.20188214 · Cited by 84
Metadata
- Authors
- Schwarzer, W., Abdennur, N., Goloborodko, A., Pekowska, A., Fudenberg, G., Loe-Mie, Y., Fonseca, N. A., Huber, W., Haering, C. H., Mirny, L., & Spitz, F.
- Affiliations
- European Molecular Biology Laboratory (DE)
- Massachusetts Institute of Technology (US)
- Centre National de la Recherche Scientifique (FR)
- European Bioinformatics Institute (GB)
- Corresponding author
- Mirny, Leonid
- ORCID
- Venue
- Nature
- Published
- 2017-09-27
- Volume
- 551
- Issue
- 7678
- Pages
- 51-56
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC5687303
- OpenAlex
- W2757387674
- Cited by
- 1,196
- References
- 78
- Citations by year
- 2026: 83 · 2025: 121 · 2024: 114 · 2023: 120 · 2022: 142 · 2021: 158 · 2020: 153 · 2019: 159 · 2018: 113 · 2017: 32
- FWCI
- 51.52
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Nature (publishedVersion)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- HAL (submittedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- DSpace@MIT (Massachusetts Institute of Technology) (submittedVersion, cc-by-nc)
- Funders
- National Science Foundation (1504942)
- European Molecular Biology Laboratory
- European Commission (305626)
- Deutsche Forschungsgemeinschaft (1331/3-1, SP 1331/3-1)
- National Institutes of Health (DK 107980)
- National Institute of General Medical Sciences (R01GM114190)
- National Institute of Diabetes and Digestive and Kidney Diseases (U54DK107980)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nuclear Structure and Function
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Chromatin Remodeling and Cancer
- Keywords
- chromatin organization, topologically associating domains, cohesin, NIPBL, loop extrusion, enhancer-promoter interactions, 3D genome organization, chromatin state, CTCF, interphase chromosomes, hepatocytes, genome compartmentalization
- MeSH terms
- Cohesins, Animals, Chromatin, Chromosomal Proteins, Non-Histone, Enhancer Elements, Genetic, Liver, Transcription Factors, Transcription, Genetic, Cell Cycle Proteins, Epigenesis, Genetic, Chromosome Positioning, Mice
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