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Chromatin structure dynamics during the mitosis-to-G1 phase transition
Open accessAbstract
Features of higher-order chromatin organization-such as A/B compartments, topologically associating domains and chromatin loops-are temporarily disrupted during mitosis 1,2. Because these structures are thought to influence gene regulation, it is important to understand how they are re-established after mitosis. Here we examine the dynamics of chromosome reorganization by Hi-C after mitosis in highly purified, synchronous mouse erythroid cell populations. We observed rapid establishment of A/B compartments, followed by their gradual intensification and expansion. Contact domains form from the 'bottom up'-smaller subTADs are formed initially, followed by convergence into multi-domain TAD structures. CTCF is partially retained on mitotic chromosomes and immediately resumes full binding in ana/telophase. By contrast, cohesin is completely evicted from mitotic chromosomes and regains focal binding at a slower rate. The formation of CTCF/cohesin co-anchored structural loops follows the kinetics of cohesin positioning. Stripe-shaped contact patterns-anchored by CTCF-grow in length, which is consistent with a loop-extrusion process after mitosis. Interactions between cis-regulatory elements can form rapidly, with rates exceeding those of CTCF/cohesin-anchored contacts. Notably, we identified a group of rapidly emerging transient contacts between cis-regulatory elements in ana/telophase that are dissolved upon G1 entry, co-incident with the establishment of inner boundaries or nearby interfering chromatin loops. We also describe the relationship between transcription reactivation and architectural features. Our findings indicate that distinct but mutually influential forces drive post-mitotic chromatin reconfiguration.
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“Cis-regulatory contacts were also shown to emerge prior to the formation of TADs in murine cells exiting mitosis [455].”
From Transcriptional enhancers and their communication with gene promoters (2021) · cites this paper as [455]
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Cites
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
Topological 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
Formation of chromosomal domains by loop extrusion
Fudenberg, G., Imakaev, M., Lu, C., Goloborodko, A., Abdennur, N., & Mirny, L. A. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.04.085 · Cited by 2,003
Sanborn, A. L., Rao, S. S. P., Huang, S.-C., Durand, N. C., Huntley, M. H., Jewett, A. I., Bochkov, I. D., Chinnappan, D., Cutkosky, A., Li, J., et al. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1518552112 · Cited by 1,730
Two independent modes of chromatin organization revealed by cohesin removal
Schwarzer, W., Abdennur, N., Goloborodko, A., Pekowska, A., Fudenberg, G., Loe-Mie, Y., Fonseca, N. A., Huber, W., Haering, C. H., Mirny, L., et al. (2017) · Nature · doi:10.1038/nature24281 · Cited by 1,196
YY1 Is a Structural Regulator of Enhancer-Promoter Loops
Weintraub, A. S., Li, C. H., Zamudio, A. V., Sigova, A. A., Hannett, N. M., Day, D. S., Abraham, B. J., Cohen, M. A., Nabet, B., Buckley, D. L., et al. (2017) · Cell · doi:10.1016/j.cell.2017.11.008 · Cited by 992
Organization of the mitotic chromosome
Naumova, N., Imakaev, M., Fudenberg, G., Zhan, Y., Lajoie, B. R., Mirny, L. A., & Dekker, J. (2013) · Science · doi:10.1126/science.1236083 · Cited by 976
Cell-cycle dynamics of chromosomal organization at single-cell resolution
Nagano, T., Lubling, Y., Várnai, C., Dudley, C., Leung, W., Baran, Y., Mendelson Cohen, N., Wingett, S., Fraser, P., & Tanay, A. (2017) · Nature · doi:10.1038/nature23001 · Cited by 794
Cohesin and CTCF differentially affect chromatin architecture and gene expression in human cells
Zuin, J., Dixon, J. R., van der Reijden, M. I. J. A., Ye, Z., Kolovos, P., Brouwer, R. W. W., van de Corput, M. P. C., van de Werken, H. J. G., Knoch, T. A., van IJcken, W. F. J., et al. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1317788111 · Cited by 779
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Thiecke, M. J., Wutz, G., Muhar, M., Tang, W., Bevan, S., Malysheva, V., Stocsits, R., Neumann, T., Zuber, J., Fraser, P., et al. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.107929 · Cited by 177
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Maksimenko, O. G., Фурсенко, Д. В., Belova, E., & Georgiev, P. G. (2021) · Acta Naturae · doi:10.32607/actanaturae.11206 · Cited by 32
Chai, H., Huang, X., Xiong, G., Huang, J., Pels, K. K., Meng, L., Han, J., Tang, D., Pan, G., Deng, L., et al. (2025) · Nature Methods · doi:10.1038/s41592-025-02658-7 · Cited by 35
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Sabaté, T., Lelandais, B., Robert, M.-C., Szalay, M., Tinevez, J.-Y., Bertrand, E., & Zimmer, C. (2025) · Nature Genetics · doi:10.1038/s41588-025-02406-9 · Cited by 32
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Malachowski, T., Chandradoss, K. R., Boya, R., Zhou, L., Cook, A. L., Chuanbin, S., Pham, K., Haws, S. A., Kim, J. H., Ryu, H.-S., et al. (2023) · Cell · doi:10.1016/j.cell.2023.11.019 · Cited by 32
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Qiu, Y., & Huang, S. (2020) · Leukemia · doi:10.1038/s41375-020-0906-x · Cited by 32
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Wiegard, A., Kuzin, V., Cameron, D. P., Grosser, J., Ceribelli, M., Mehmood, R., Ballarino, R., Valant, F., Grochowski, R., Karabogdan, I., et al. (2021) · Molecular Cell · doi:10.1016/j.molcel.2021.10.015 · Cited by 31
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Alagna, N. S., Thomas, T. I., Wilson, K. L., & Reddy, K. L. (2023) · FEBS Letters · doi:10.1002/1873-3468.14771 · Cited by 31
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Goel, V. Y., Aboreden, N. G., Jusuf, J. M., Zhang, H., Mori, L., Mirny, L. A., Blobel, G. A., Banigan, E. J., & Hansen, A. S. (2025) · Nature Structural & Molecular Biology · doi:10.1038/s41594-025-01687-2 · Cited by 35
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Rullens, P. M. J., & Kind, J. (2020) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2020.11.006 · Cited by 26
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Naso, F. D., Sterbini, V., Crecca, E., Asteriti, I. A., Russo, A. D., Giubettini, M., Cundari, E., Lindon, C., Rosa, A., & Guarguaglini, G. (2020) · Cells · doi:10.3390/cells9020374 · Cited by 30
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Li, D., Wu, F., Zhou, S., Huang, X., & Lee, H. (2023) · Nature Structural & Molecular Biology · doi:10.1038/s41594-023-00939-3 · Cited by 28
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Oji, A., Choubani, L., Miura, H., & Hiratani, I. (2024) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2024.102406 · Cited by 28
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Liu, N. Q., Magnitov, M. D., Schijns, M. M. G. A., van Schaik, T., Teunissen, H., van Steensel, B., & de Wit, E. (2025) · Nucleic Acids Research · doi:10.1093/nar/gkaf549 · Cited by 33
Precise measurements of chromatin diffusion dynamics by modeling using Gaussian processes
Oliveira, G. M., Oravecz, A., Kobi, D., Maroquenne, M., Bystricky, K., Sexton, T., & Molina, N. (2021) · Nature Communications · doi:10.1038/s41467-021-26466-7 · Cited by 23
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Zhou, R., Tian, K., Huang, J. S., Duan, W., Fu, H., Feng, Y., Wang, H., Jiang, Y., Li, Y., Wang, R., et al. (2022) · iScience · doi:10.1016/j.isci.2022.105011 · Cited by 26
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Chervova, A. A., Festuccia, N., Altamirano‐Pacheco, L., Dubois, A., & Navarro, P. (2022) · EMBO Reports · doi:10.15252/embr.202256075 · Cited by 27
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Brunner, A., Morero, N. R., Zhang, W., Hossain, M. J., Lampe, M., Pflaumer, H., Halavatyi, A. A., Peters, J., Beckwith, K. S., & Ellenberg, J. (2024) · The Journal of Cell Biology · doi:10.1083/jcb.202405169 · Cited by 24
Bonora, G., Ramani, V., Singh, R., Fang, H., Jackson, D. L., Srivatsan, S. R., Qiu, R., Lee, C., Trapnell, C., Shendure, J., et al. (2021) · Genome biology · doi:10.1186/s13059-021-02432-w · Cited by 26
Genome folding principles uncovered in condensin-depleted mitotic chromosomes
Zhao, H., Lin, Y., Lin, E., Liu, F., Shu, L., Jing, D., Wang, B., Wang, M., Shan, F., Zhang, L., et al. (2024) · Nature Genetics · doi:10.1038/s41588-024-01759-x · Cited by 26
Self-citationConformational state switching and pathways of chromosome dynamics in cell cycle
Chu, X., & Wang, J. (2020) · Applied Physics Reviews · doi:10.1063/5.0007316 · Cited by 24
Rappoport, N., Chomsky, E., Nagano, T., Seibert, C., Lubling, Y., Baran, Y., Lifshitz, A., Leung, W., Mukamel, Z., Ron Shamir, A., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-39549-4 · Cited by 25
Xu, J., Xu, X., Huang, D., Luo, Y., Lin, L., Bai, X., Zheng, Y., Yang, Q., Cheng, Y., Huang, A., et al. (2024) · Nature Communications · doi:10.1038/s41467-024-48593-7 · Cited by 25
Building the genome architecture during the maternal to zygotic transition
Zhang, Y., & Xie, W. (2021) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2021.11.002 · Cited by 25
Ramos-Alonso, L., Holland, P., Gras, S. L., Zhao, X., Jost, B., Bjørås, M., Barral, Y., Enserink, J. M., & Chymkowitch, P. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2210593120 · Cited by 24
Dynamics and regulation of mitotic chromatin accessibility bookmarking at single-cell resolution
Yu, Q., Liu, X., Fang, J., Wu, H., Guo, C., Zhang, W., Liu, N., Jiang, C., Sha, Q., Yuan, X. N., et al. (2023) · Science Advances · doi:10.1126/sciadv.add2175 · Cited by 26
Metadata
- Authors
- Zhang, H., Emerson, D. J., Gilgenast, T. G., Titus, K. R., Lan, Y., Huang, P., Zhang, D., Wang, H., Keller, C. A., Giardine, B., Hardison, R. C., Phillips-Cremins, J. E., & Blobel, G. A.
- Affiliations
- Children's Hospital of Philadelphia (US)
- University of Pennsylvania (US)
- Pennsylvania State University (US)
- Corresponding author
- Blobel, Gerd A.
- ORCID
- Venue
- Nature
- Published
- 2019-11-27
- Volume
- 576
- Issue
- 7785
- Pages
- 158-162
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC6895436
- OpenAlex
- W2990380375
- Cited by
- 271
- References
- 27
- Citations by year
- 2026: 31 · 2025: 57 · 2024: 28 · 2023: 45 · 2022: 31 · 2021: 48 · 2020: 29 · 2019: 2
- FWCI
- 9.68
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- National Institutes of Health
- National Heart, Lung, and Blood Institute (U01HL129998)
- National Institute of Mental Health (DP2MH110247)
- National Institute of Diabetes and Digestive and Kidney Diseases (R37DK058044, R01DK058044, R24DK106766)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Chromatin Remodeling and Cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nuclear Structure and Function
- Keywords
- chromatin reorganization, A/B compartments, topologically associating domains, CTCF, cohesin, chromatin looping, loop extrusion, erythroid cells
- MeSH terms
- Cohesins, Animals, Chromatin, Chromosomal Proteins, Non-Histone, Mitosis, G1 Phase, Cell Cycle Proteins, Mice
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