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Spatial partitioning of the regulatory landscape of the X-inactivation centre
Open accessAbstract
In eukaryotes transcriptional regulation often involves multiple long-range elements and is influenced by the genomic environment. A prime example of this concerns the mouse X-inactivation centre (Xic), which orchestrates the initiation of X-chromosome inactivation (XCI) by controlling the expression of the non-protein-coding Xist transcript. The extent of Xic sequences required for the proper regulation of Xist remains unknown. Here we use chromosome conformation capture carbon-copy (5C) and super-resolution microscopy to analyse the spatial organization of a 4.5-megabases (Mb) region including Xist. We discover a series of discrete 200-kilobase to 1 Mb topologically associating domains (TADs), present both before and after cell differentiation and on the active and inactive X. TADs align with, but do not rely on, several domain-wide features of the epigenome, such as H3K27me3 or H3K9me2 blocks and lamina-associated domains. TADs also align with coordinately regulated gene clusters. Disruption of a TAD boundary causes ectopic chromosomal contacts and long-range transcriptional misregulation. The Xist/Tsix sense/antisense unit illustrates how TADs enable the spatial segregation of oppositely regulated chromosomal neighbourhoods, with the respective promoters of Xist and Tsix lying in adjacent TADs, each containing their known positive regulators. We identify a novel distal regulatory region of Tsix within its TAD, which produces a long intervening RNA, Linx. In addition to uncovering a new principle of cis-regulatory architecture of mammalian chromosomes, our study sets the stage for the full genetic dissection of the X-inactivation centre.
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“Consistent with prior studies16, we found that genes in the same domain correlate across samples, but that genes separated by a boundary show lower correlation (Fig. 1e).”
From Insulator dysfunction and oncogene activation in IDH mutant gliomas (2016) · cites this paper as [16]
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
“Consistent with prior studies16, we found that genes in the same domain correlate across samples, but that genes separated by a boundary show lower correlation (Fig. 1e).”
From Insulator dysfunction and oncogene activation in IDH mutant gliomas (2016) · cites this paper as [16]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“metazoan genomes are organised into megabase-scale segregated domains that are often invariant between cell types, termed topologically associating domains (TADs) [432–434].”
From Transcriptional enhancers and their communication with gene promoters (2021) · cites this paper as [433]
The cited source says what the claim attributes to it.
In the citing paper
“Second, it was demonstrated that eukaryotic chromosomes are partitioned into so-called topologically associated domains (TADs) [35,36,37], which appear to restrict the areas of enhancer action [38,39,40,41].”
From Enhancer Function in the 3D Genome (2023) · cites this paper as [35]
In the citing paper
“Indeed, the genome is now known to be hierarchically organized in a series of 3D structures, starting from nucleosome clutches, to chromatin loops, to chromosomal domains called topologically associating domains (TADs), and finally to active or repressive compartments and chromosome territories 15,46,[48][49][50] .”
From Advances in epigenetics link genetics to the environment and disease (2019) · cites this paper as [48]
In the citing paper
“These changes enable proceeding through the 3C protocol in a single tube per sample, allow handling of over 20 samples in parallel, reduce the amount of cells needed by a factor 5 to 10 and cut down the time needed to complete the protocol from 8 days (Nora et al. 2012) to 4 days.”
From Targeted Degradation of CTCF Decouples Local Insulation of Chromosome Domains from Genomic Compartmentalization (2017) · cites this paper as Nora et al. 2012
In the citing paper
“loop extrusion mediated by cohesin and CTCF mediates the formation of chromatin loops and self-interacting Topologically Associating Domains (TADs)”
From Neuronal DNA double-strand breaks lead to genome structural variations and 3D genome disruption in neurodegeneration (2023) · cites this paper as [85]
In the citing paper
“Mammalian genomes are organized into a hierarchy of Megabase (Mb)-scale topologically associating domains (TADs) (Dixon et al., 2012; Nora et al., 2012) and smaller, nested subTADs (Dixon et al., 2012; Nora et al., 2012; Phillips-Cremins et al., 2013; Rao et al., 2014).”
From Disease-Associated Short Tandem Repeats Co-localize with Chromatin Domain Boundaries (2018) · cites this paper as Nora et al., 2012
In the citing paper
“Consistent with previous reports, we found enrichment for the architectural protein CCCTC-binding factor (CTCF) at human ES cell boundaries compared to loci internal to domains (Figure S6A-B) (Dixon et al., 2012; Nora et al., 2012; Phillips-Cremins et al., 2013).”
From Disease-Associated Short Tandem Repeats Co-localize with Chromatin Domain Boundaries (2018) · cites this paper as Nora et al., 2012
In the citing paper
“The deposition of chromatin marks is thought to contribute to this process (Dixon et al., 2015, Nora et al., 2012)”
From Multiscale 3D Genome Rewiring during Mouse Neural Development (2017) · cites this paper as Nora et al., 2012
In the citing paper
“At intermediate scales (100 kb to 1 Mb), a major discovery is the existence of topologically associating domains (TADs) (Dixon et al., 2012, Nora et al., 2012, Sexton et al., 2012).”
From Multiscale 3D Genome Rewiring during Mouse Neural Development (2017) · cites this paper as Nora et al., 2012
In the citing paper
“Recent chromosome conformation studies have revealed that mammalian chromosomes are structured into largely tissue-invariant TADs in which the DNA interactions are more frequent within a given domain than with regions in other domains4,5.”
From Disruption of chromatin folding domains by somatic genomic rearrangements in human cancer (2020) · cites this paper as [5]
In the citing paper
“The disruption of domain boundaries can result in ectopic interactions between neighboring domains and affect the regulation of nearby genes5,9.”
From Disruption of chromatin folding domains by somatic genomic rearrangements in human cancer (2020) · cites this paper as [5]
In the citing paper
“TADs were identified through Hi-C3,4 and their existence have since been confirmed by alternative methods such as intrinsic 3C (i3C),18 which avoids the cross-linking step and Genome Architecture Mapping (GAM),19 which avoids the ligation step.”
From Recent evidence that TADs and chromatin loops are dynamic structures (2018) · cites this paper as [3]
In the citing paper
“First, chromatin is organized into Topological Associating Domains (TADs) that are characterized by preferential contacts between loci inside the same TAD and insulation from loci in adjacent TADs.3,4”
From Recent evidence that TADs and chromatin loops are dynamic structures (2018) · cites this paper as [3]
In the citing paper
“A large body of evidence suggests that TADs correspond to functional regulatory domains by primarily restricting contact between enhancers and promoters to occur within the same TAD3,21–25”
From Recent evidence that TADs and chromatin loops are dynamic structures (2018) · cites this paper as [3]
In the citing paper
“Accordingly, deletion of a boundary between two TADs causes ectopic contacts between previously insulated loci3 and can cause aberrant gene expression through improper enhancer-promoter contact.27,28”
From Recent evidence that TADs and chromatin loops are dynamic structures (2018) · cites this paper as [3]
In the citing paper
“suggesting an important functional role of CTCF and cohesin in TAD formation and maintenance (Fig. 2A).”
From Recent evidence that TADs and chromatin loops are dynamic structures (2018) · cites this paper as [3]
In the citing paper
“Both DNA FISH3,9,36–39 and single-cell Hi-C40,41 studies show that genome organization is highly variable between cells and that even strong Hi-C loop anchors only contact in a small subset of cells”
From Recent evidence that TADs and chromatin loops are dynamic structures (2018) · cites this paper as [3]
In the citing paper
“After TADs were discovered through Hi-C studies, it quickly became clear that TAD boundaries are near universally enriched in CTCF and cohesin ChIP-Seq peaks,3,4,16”
From Recent evidence that TADs and chromatin loops are dynamic structures (2018) · cites this paper as [3]
In the citing paper
“The CTCF/cohesin anchored loop domain matching the Hi-C corner-peak actually only exists in a small subset of cells, which is also consistent with the high levels of cell-to-cell variability in contact probability observed in DNA FISH studies.3,9,36–39”
From Recent evidence that TADs and chromatin loops are dynamic structures (2018) · cites this paper as [3]
In the citing paper
“Furthermore, individual chromosomes are partitioned into megabase- sized topologically associating domains (TADs), regions with relatively high intradomain DNA interaction frequencies as measured by Hi-C chromosome conformation capture data (Dixon et al., 2012; Nora et al., 2012).”
From Insulated Neighborhoods: Structural and Functional Units of Mammalian Gene Control (2016) · cites this paper as Nora et al., 2012
In the citing paper
“Nonetheless, the TADs identified by processing Hi-C data with the Hidden Markov algorithm (Dixon et al., 2012; Nora et al., 2012) can also be identified when this algorithm is used to process cohesin ChIA-PET data (Ji et al., 2016).”
From Insulated Neighborhoods: Structural and Functional Units of Mammalian Gene Control (2016) · cites this paper as Nora et al., 2012
In the citing paper
“genome-wide, high-resolution understanding of chromosome cell-cycle dynamics11 is still limited by current technologies”
From Cell-cycle dynamics of chromosomal organization at single-cell resolution (2017) · cites this paper as [4]
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Cites
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
Chromatin signature reveals over a thousand highly conserved large non-coding RNAs in mammals
Guttman, M., Amit, I., Garber, M., French, C., Lin, M. F., Feldser, D., Huarte, M., Zuk, O., Carey, B. W., Cassady, J. P., et al. (2009) · Nature · doi:10.1038/nature07672 · Cited by 4,098
Khalil, A. M., Guttman, M., Huarte, M., Garber, M., Raj, A., Rivea Morales, D., Thomas, K., Presser, A., Bernstein, B. E., van Oudenaarden, A., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0904715106 · Cited by 2,872
Three-dimensional folding and functional organization principles of the Drosophila genome
Sexton, T., Yaffe, E., Kenigsberg, E., Bantignies, F., Leblanc, B., Hoichman, M., Parrinello, H., Tanay, A., & Cavalli, G. (2012) · Cell · doi:10.1016/j.cell.2012.01.010 · Cited by 1,983
Mediator and cohesin connect gene expression and chromatin architecture
Kagey, M. H., Newman, J. J., Bilodeau, S., Zhan, Y., Orlando, D. A., van Berkum, N. L., Ebmeier, C. C., Goossens, J., Rahl, P. B., Levine, S. S., et al. (2010) · Nature · doi:10.1038/nature09380 · Cited by 1,939
Self-citationDostie, J., Richmond, T., Arnaout, R., Selzer, R. R., Lee, W. L., Honan, T., Rubio, E. D., Krumm, A., Lamb, J., Nusbaum, C., et al. (2006) · Genome Research · doi:10.1101/gr.5571506 · Cited by 1,237
Self-citationMolecular Maps of the Reorganization of Genome-Nuclear Lamina Interactions during Differentiation
Peric-Hupkes, D., Meuleman, W., Pagie, L., Bruggeman, S. W. M., Solovei, I., Brugman, W., Gräf, S., Flicek, P., Kerkhoven, R. M., van Lohuizen, M., et al. (2010) · Molecular Cell · doi:10.1016/j.molcel.2010.03.016 · Cited by 1,050
Distinct epigenomic landscapes of pluripotent and lineage-committed human cells
Hawkins, R. D., Hon, G. C., Lee, L. K., Ngo, Q., Lister, R., Pelizzola, M., Edsall, L. E., Kuan, S., Luu, Y., Klugman, S., et al. (2010) · Cell stem cell · doi:10.1016/j.stem.2010.03.018 · Cited by 806
The Human Transcriptome Map: Clustering of Highly Expressed Genes in Chromosomal Domains
Caron, H. N., van Schaik, B. D. C., van der Mee, M., Baas, F., Riggins, G. J., Sluis, P. V., Hermus, M.-C., van Asperen, R., Boon, K., Voûte, P. A., et al. (2001) · Science · doi:10.1126/science.1056794 · Cited by 730
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HiFive: a tool suite for easy and efficient HiC and 5C data analysis
Sauria, M. E. G., Phillips‐Cremins, J. E., Corces, V. G., & Taylor, J. (2015) · Genome biology · doi:10.1186/s13059-015-0806-y · Cited by 60
Junier, I., Boccard, F., & Espéli, O. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt1005 · Cited by 59
Spectral identification of topological domains
Chen, J., Hero, A. O., & Rajapakse, I. (2016) · Bioinformatics · doi:10.1093/bioinformatics/btw221 · Cited by 59
Dong, P., Tu, X., Liang, Z., Kang, B., & Zhong, S. (2020) · Journal of Experimental Botany · doi:10.1093/jxb/eraa220 · Cited by 60
Iwasaki, O., Tanizawa, H., Kim, K.-D., Kossenkov, A., Nacarelli, T., Tashiro, S., Majumdar, S., Showe, L. C., Zhang, R., & Noma, K.-I. (2019) · Nature Communications · doi:10.1038/s41467-019-13604-5 · Cited by 58
Yeung, J., & Naef, F. (2018) · Trends in Genetics · doi:10.1016/j.tig.2018.09.005 · Cited by 61
Understanding Spatial Genome Organization: Methods and Insights
Ramani, V., Shendure, J., & Duan, Z. (2016) · Genomics Proteomics & Bioinformatics · doi:10.1016/j.gpb.2016.01.002 · Cited by 66
Lee, D. P., Tan, W. L. W., Anene-Nzelu, C. G., Lee, C. J. M., Li, P. Y., Luu, T. D. A., Chan, C. X., Tiang, Z., Ng, S. L., Huang, X., et al. (2019) · Circulation · doi:10.1161/circulationaha.118.036726 · Cited by 61
The genome-wide multi-layered architecture of chromosome pairing in early Drosophila embryos
Erceg, J., Abed, J. A., Goloborodko, A. A., Lajoie, B. R., Fudenberg, G., Abdennur, N. A., Imakaev, M., McCole, R. B., Nguyen, S. C., Saylor, W., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-12211-8 · Cited by 59
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Norton, H. K., & Phillips-Cremins, J. E. (2017) · Journal of Cell Biology · doi:10.1083/jcb.201611001 · Cited by 57
Recent advances in X-chromosome inactivation research
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LncRNA Jpx induces Xist expression in mice using both trans and cis mechanisms
Carmona, S., Lin, B., Chou, T., Arroyo, K., & Sun, S. (2018) · PLoS Genetics · doi:10.1371/journal.pgen.1007378 · Cited by 57
Pan-3D genome analysis reveals structural and functional differentiation of soybean genomes
Ni, L., Liu, Y.-C., Ma, X., Liu, T.-F., Yang, X., Wang, Z., Liang, Q.-J., Liu, S.-L., Zhang, M., Wang, Z., et al. (2023) · Genome Biology · doi:10.1186/s13059-023-02854-8 · Cited by 53
Zhong, J., Niu, L., Lin, Z., Bai, X., Chen, Y., Luo, F., Hou, C., & Xiao, C. (2023) · Nature Communications · doi:10.1038/s41467-023-36899-x · Cited by 58
Multiplex-GAM: genome-wide identification of chromatin contacts yields insights overlooked by Hi-C
Beagrie, R. A., Thieme, C. J., Annunziatella, C., Baugher, C., Zhang, Y., Schueler, M., Kukalev, A., Kempfer, R., Chiariello, A. M., Bianco, S., et al. (2023) · Nature Methods · doi:10.1038/s41592-023-01903-1 · Cited by 61
Breaking TADs: Insights into Hierarchical Genome Organization
Rocha, P. P., Raviram, R., Bonneau, R., & Skok, J. A. (2015) · Epigenomics · doi:10.2217/epi.15.25 · Cited by 58
Multiple dimensions of epigenetic gene regulation in the malaria parasite Plasmodium falciparum
Ay, F., Bunnik, E. M., Varoquaux, N., Vert, J., Noble, W. S., & Roch, K. G. L. (2014) · BioEssays · doi:10.1002/bies.201400145 · Cited by 60
Barutcu, A. R., Fritz, A. J., Zaidi, S. K., van Wijnen, A. J., Lian, J. B., Stein, J. L., Nickerson, J. A., Imbalzano, A. N., & Stein, G. S. (2015) · Journal of Cellular Physiology · doi:10.1002/jcp.25062 · Cited by 63
Zhang, B., & Wolynes, P. G. (2016) · Biophysical Journal · doi:10.1016/j.bpj.2016.08.046 · Cited by 57
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Sartorelli, V., & Puri, P. (2018) · Molecular Cell · doi:10.1016/j.molcel.2018.04.025 · Cited by 59
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Sikorska, N., & Sexton, T. (2019) · Journal of Molecular Biology · doi:10.1016/j.jmb.2019.12.006 · Cited by 65
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dos Santos, Á., & Toseland, C. P. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22063178 · Cited by 59
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Sood, V., & Misteli, T. (2021) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2021.10.004 · Cited by 53
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Rafique, S., Thomas, J. S. J., Sproul, D., & Bickmore, W. A. (2015) · Genome biology · doi:10.1186/s13059-015-0719-9 · Cited by 60
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Jerković, I., Szabo, Q., Bantignies, F., & Cavalli, G. (2019) · Journal of Molecular Biology · doi:10.1016/j.jmb.2019.10.014 · Cited by 57
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Tena, J. J., & Santos-Pereira, J. M. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.702787 · Cited by 65
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Pachano, T., Haro, E., & Rada-Iglesias, Á. (2022) · Development · doi:10.1242/dev.186536 · Cited by 57
tDNA insulators and the emerging role of TFIIIC in genome organization
Bortle, K. V., & Corces, V. G. (2012) · Transcription · doi:10.4161/trns.21579 · Cited by 55
Furlan, G., & Rougeulle, C. (2016) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1359 · Cited by 55
X chromosome inactivation: silencing, topology and reactivation
Robert-Finestra, T., & Gribnau, J. H. (2017) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2017.01.007 · Cited by 59
Self-citationDoynova, M., Markworth, J. F., Cameron‐Smith, D., Vickers, M. H., & O'Sullivan, J. M. (2017) · Skeletal Muscle · doi:10.1186/s13395-017-0122-1 · Cited by 55
Račko, D., Benedetti, F., Dorier, J., & Stasiak, A. (2018) · Nucleic Acids Research · doi:10.1093/nar/gky1091 · Cited by 58
Amat, R., Böttcher, R., Dily, F. L., Vidal, E., Quilez, J., Cuartero, Y., Beato, M., de Nadal, E., & Posas, F. (2018) · Genome Research · doi:10.1101/gr.238527.118 · Cited by 58
Three-dimensional organization and dynamics of the genome
Szałaj, P., & Plewczyński, D. (2018) · Cell Biology and Toxicology · doi:10.1007/s10565-018-9428-y · Cited by 59
Soochit, W., Sleutels, F., Stik, G., Bartkuhn, M., Basu, S., Hernández, S. C., Merzouk, S., Vidal, E., Boers, R., Boers, J., et al. (2021) · Nature Cell Biology · doi:10.1038/s41556-021-00722-w · Cited by 55
Self-citationChromatin Architectures and Hox Gene Collinearity
Noordermeer, D., & Duboule, D. (2013) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/b978-0-12-416027-9.00004-8 · Cited by 54
Chromatin organization: form to function
de Graaf, C. A., & van Steensel, B. (2012) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2012.11.011 · Cited by 59
Fritz, A. J., Ghule, P. N., Boyd, J. R., Tye, C., Page, N., Hong, D., Shirley, D. J., Weinheimer, A. S., Barutcu, A. R., Gerrard, D., et al. (2017) · Journal of Cellular Physiology · doi:10.1002/jcp.25996 · Cited by 44
3D genome organization: a role for phase separation and loop extrusion?
Stam, M. E., Tark‐Dame, M., & Fransz, P. F. (2019) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2019.03.008 · Cited by 54
Chromosome disentanglement driven via optimal compaction of loop-extruded brush structures
Brahmachari, S., & Marko, J. F. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1906355116 · Cited by 54
Epigenetic editing: Dissecting chromatin function in context
Policarpi, C., Dabin, J., & Hackett, J. A. (2021) · BioEssays · doi:10.1002/bies.202000316 · Cited by 54
Bauer, M., Vidal, E., Zorita, E. V., Üresin, N., Pinter, S. F., Filion, G. J. P., & Payer, B. (2021) · Nature Communications · doi:10.1038/s41467-021-23610-1 · Cited by 54
Chromatin architecture reorganization during neuronal cell differentiation in Drosophila genomePreprint
Chathoth, K. T., & Zabet, N. R. (2019) · Genome Research · doi:10.1101/gr.246710.118 · Cited by 56
Renschler, G., Richard, G., Valsecchi, C. I. K., Toscano, S., Arrigoni, L., Ramírez, F., & Akhtar, A. (2019) · Genes & Development · doi:10.1101/gad.328971.119 · Cited by 54
Old cells, new tricks: chromatin structure in senescence
Parry, A. J., & Narita, M. (2016) · Mammalian Genome · doi:10.1007/s00335-016-9628-9 · Cited by 53
Feng, Y., Cai, L., Hong, W., Zhang, C., Tan, N., Wang, M., Wang, C., Liu, F., Wang, X., Ma, J., et al. (2022) · Circulation · doi:10.1161/circulationaha.121.055781 · Cited by 56
Gene regulation on extrachromosomal DNA
Hung, K. L., Mischel, P. S., & Chang, H. Y. (2022) · Nature Structural & Molecular Biology · doi:10.1038/s41594-022-00806-7 · Cited by 56
Showpnil, I. A., Selich‐Anderson, J., Taslim, C., Boone, M. A., Crow, J. C., Theisen, E. R., & Lessnick, S. L. (2022) · Nucleic Acids Research · doi:10.1093/nar/gkac747 · Cited by 59
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Zhang, P., & Wu, H. (2023) · IEEE Journal of Biomedical and Health Informatics · doi:10.1109/jbhi.2023.3292299 · Cited by 53
Calandrelli, R., Wen, X., Richard, J. L. C., Luo, Z., Nguyen, T. C., Chen, C.-J., Qi, Z., Xue, S., Chen, W., Yan, Z., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-42274-7 · Cited by 55
Spatial Regulation of V–(D)J Recombination at Antigen Receptor Loci
Ebert, A., Hill, L., & Busslinger, M. (2015) · Advances in immunology · doi:10.1016/bs.ai.2015.07.006 · Cited by 61
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Wolle, D. G., Cléard, F., Aoki, T., Deshpande, G., Schedl, P. D., & Karch, F. (2015) · Molecular and Cellular Biology · doi:10.1128/mcb.00456-15 · Cited by 53
Wachsmuth, M., Knoch, T., & Rippe, K. (2016) · Epigenetics & Chromatin · doi:10.1186/s13072-016-0093-1 · Cited by 55
Predicting chromatin architecture from models of polymer physics
Bianco, S., Chiariello, A. M., Annunziatella, C., Esposito, A., & Nicodemi, M. (2017) · Chromosome Research · doi:10.1007/s10577-016-9545-5 · Cited by 53
Computational 3D genome modeling using Chrom3D
Paulsen, J., Ali, T. M. L., & Collas, P. (2018) · Nature Protocols · doi:10.1038/nprot.2018.009 · Cited by 55
Rhie, S., Schreiner, S., Witt, H., Armoskus, C., Lay, F. D., Camarena, A., Spitsyna, V. N., Guo, Y., Berman, B. P., Evgrafov, O., et al. (2018) · Science Advances · doi:10.1126/sciadv.aav8550 · Cited by 50
de Wit, E. (2019) · Journal of Molecular Biology · doi:10.1016/j.jmb.2019.09.026 · Cited by 57
Chromatin topology and the timing of enhancer function at the HoxD locus
Rodríguez-Carballo, E., Lopez‐Delisle, L., Willemin, A., Beccari, L. L., Gitto, S., Mascrez, B., & Duboule, D. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2015083117 · Cited by 54
Chromatin Remodelers in the 3D Nuclear Compartment
Magaña‐Acosta, M., & Valadéz-Graham, V. (2020) · Frontiers in Genetics · doi:10.3389/fgene.2020.600615 · Cited by 58
TGFβ promotes widespread enhancer chromatin opening and operates on genomic regulatory domains
Guerrero-Martinez, J. A., Ceballos-Chávez, M., Koehler, F., Peiró, S., & Reyes, J. C. (2020) · Nature Communications · doi:10.1038/s41467-020-19877-5 · Cited by 56
3D chromatin architecture and epigenetic regulation in cancer stem cells
Feng, Y., Liu, X., & Pauklin, S. (2021) · Protein & Cell · doi:10.1007/s13238-020-00819-2 · Cited by 55
Collas, P., Lund, E. G., & Oldenburg, A. R. (2013) · BioEssays · doi:10.1002/bies.201300138 · Cited by 55
3D genome, on repeat: Higher-order folding principles of the heterochromatinized repetitive genome
Haws, S. A., Simándi, Z., Barnett, R. J., & Phillips‐Cremins, J. E. (2022) · Cell · doi:10.1016/j.cell.2022.06.052 · Cited by 55
Minkovsky, A., Barakat, T. S., Sellami, N., Chin, M. H., Gunhanlar, N., Gribnau, J. H., & Plath, K. (2013) · Cell Reports · doi:10.1016/j.celrep.2013.02.018 · Cited by 51
Self-citationA mechanistic link between gene regulation and genome architecture in mammalian development
Bonora, G., Plath, K., & Denholtz, M. (2014) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2014.05.002 · Cited by 52
Chen, C., Chang, I., Hsiung, C. A., & Wasserman, W. W. (2014) · BMC Medical Genomics · doi:10.1186/1755-8794-7-34 · Cited by 51
Neems, D. S., Garza-Gongora, A. G., Smith, E. D., & Kosak, S. T. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1521826113 · Cited by 51
Anderson, E. C., Frankino, P. A., Higuchi‐Sanabria, R., Yang, Q., Bian, Q., Podshivalova, K., Shin, A., Kenyon, C. J., Dillin, A. G., & Meyer, B. J. (2019) · Developmental Cell · doi:10.1016/j.devcel.2019.08.004 · Cited by 51
Abnormal X chromosome inactivation and tumor development
Wang, D., Tang, L. M., Wu, Y., Fan, C., Zhang, S., Xiang, B., Zhou, M., Li, X., Li, Y., Li, G., et al. (2020) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-020-03469-z · Cited by 51
A WIZ/Cohesin/CTCF Complex Anchors DNA Loops to Define Gene Expression and Cell Identity
Justice, M., Carico, Z. M., Stefan, H. C., & Dowen, J. M. (2020) · Cell Reports · doi:10.1016/j.celrep.2020.03.067 · Cited by 51
Epigenomics and the structure of the living genomePreprint
Friedman, N., & Rando, O. J. (2015) · Genome Research · doi:10.1101/gr.190165.115 · Cited by 54
The Molecular and Nuclear Dynamics of X-Chromosome InactivationPreprint
Dossin, F., & Heard, É. (2021) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a040196 · Cited by 59
Watson, L. A., & Tsai, L. (2016) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2016.12.002 · Cited by 52
Cohesin mediates DNA loop extrusion and sister chromatid cohesion by distinct mechanisms
Nagasaka, K., Davidson, I. F., Stocsits, R. R., Tang, W., Wutz, G., Batty, P., Panarotto, M., Litos, G., Schleiffer, A., Gerlich, D. W., et al. (2023) · Molecular Cell · doi:10.1016/j.molcel.2023.07.024 · Cited by 53
Epigenetics in the modern era of crop improvements
Xue, Y., Cao, X., Chen, X., Deng, X. M., Deng, X. W., Ding, Y., Dong, A., Duan, C., Fang, X., Gong, L., et al. (2025) · Science China Life Sciences · doi:10.1007/s11427-024-2784-3 · Cited by 52
Regulation of Chromatin Structure During Neural Development
Kishi, Y., & Gotoh, Y. (2018) · Frontiers in Neuroscience · doi:10.3389/fnins.2018.00874 · Cited by 51
Rennie, S., Dalby, M., van Duin, L., & Andersson, R. (2018) · Nature Communications · doi:10.1038/s41467-017-02798-1 · Cited by 55
Polymer physics of nuclear organization and function
Amitai, A., & Holcman, D. (2017) · Physics Reports · doi:10.1016/j.physrep.2017.02.002 · Cited by 53
RNA proximity sequencing reveals the spatial organization of the transcriptome in the nucleus
Morf, J., Wingett, S., Farabella, I., Cairns, J., Furlan-Magaril, M., Jiménez‐García, L. F., Liu, X., Craig, F. F., Walker, S. A., Segonds-Pichon, A., et al. (2019) · Nature Biotechnology · doi:10.1038/s41587-019-0166-3 · Cited by 51
The 3D Genome Structure of Single Cells
Zhou, T., Zhang, R., & Ma, J. (2021) · Annual Review of Biomedical Data Science · doi:10.1146/annurev-biodatasci-020121-084709 · Cited by 51
Flexible and dynamic nucleosome fiber in living mammalian cells
Nozaki, T., Kaizu, K., Pack, C., Tamura, S., Tani, T., Hihara, S., Nagai, T., Takahashi, K., & Maeshima, K. (2013) · Nucleus · doi:10.4161/nucl.26053 · Cited by 50
Szałaj, P., Tang, Z., Michalski, P. J., Pietal, M. J., Luo, O. J., Sadowski, M., Li, X., Radew, K., Ruan, Y., & Plewczyński, D. (2016) · Genome Research · doi:10.1101/gr.205062.116 · Cited by 50
Franke, M., Daly, A., Palmeira, L., Tirosh, A., Stigliano, A., Trifan, E., Faucz, F. R., Abboud, D., Pétrossians, P., Tena, J. J., et al. (2022) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2022.02.002 · Cited by 50
Range extender mediates long-distance enhancer activity
Bower, G., Hollingsworth, E. W., Jacinto, S. H., Alcantara, J. A., Clock, B., Cao, K., Liu, M., Dziulko, A., Alcaina-Caro, A., Xu, Q., et al. (2025) · Nature · doi:10.1038/s41586-025-09221-6 · Cited by 49
Schwarzer, W., & Spitz, F. (2014) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2014.03.014 · Cited by 52
From single genes to entire genomes: the search for a function of nuclear organization
Pueschel, R., Coraggio, F., & Meister, P. (2016) · Development · doi:10.1242/dev.129007 · Cited by 52
The Emerging Role of the Cytoskeleton in Chromosome Dynamics
Spichal, M., & Fabre, E. (2017) · Frontiers in Genetics · doi:10.3389/fgene.2017.00060 · Cited by 54
Bortle, K. V., Phanstiel, D. H., & Snyder, M. P. (2017) · Genome biology · doi:10.1186/s13059-017-1310-3 · Cited by 53
The long-range interaction map of ribosomal DNA arrays
Yu, S., & Lemos, B. (2018) · PLoS Genetics · doi:10.1371/journal.pgen.1007258 · Cited by 53
Function and regulation of chromatin insulators in dynamic genome organization
Chen, D., & Lei, E. P. (2019) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2019.02.001 · Cited by 52
Dynamics of sister chromatid resolution during cell cycle progression
Stanytė, R., Nuebler, J., Blaukopf, C., Hoefler, R., Stocsits, R. R., Peters, J., & Gerlich, D. W. (2018) · The Journal of Cell Biology · doi:10.1083/jcb.201801157 · Cited by 49
Amândio, A. R., Beccari, L. L., Lopez‐Delisle, L., Mascrez, B., Zákány, J., Gitto, S., & Duboule, D. (2021) · Genes & Development · doi:10.1101/gad.348934.121 · Cited by 49
Chovanec, P., Collier, A. J., Krueger, C., Várnai, C., Semprich, C. I., Schoenfelder, S., Corcoran, A. E., & Rugg‐Gunn, P. J. (2021) · Nature Communications · doi:10.1038/s41467-021-22201-4 · Cited by 48
The 3D enhancer network of the developing T cell genome is shaped by SATB1
Ζελένκα, Τ., Klonizakis, A., Tsoukatou, D., Papamatheakis, D.-A., Franzenburg, S., Tzerpos, P., Tzonevrakis, I.-R., Papadogkonas, G., Kapsetaki, M., Nikolaou, C., et al. (2022) · Nature Communications · doi:10.1038/s41467-022-34345-y · Cited by 50
Evolution of 3D chromatin organization at different scales
Acemel, R. D., & Lupiáñez, D. G. (2023) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2022.102019 · Cited by 50
Metadata
- Authors
- Nora, E. P., Lajoie, B. R., Schulz, E. G., Giorgetti, L., Okamoto, I., Servant, N., Piolot, T., van Berkum, N. L., Meisig, J., Sedat, J., Gribnau, J., Barillot, E., Blüthgen, N., Dekker, J., & Heard, E.
- Affiliations
- Institut Curie (FR)
- University of Massachusetts Chan Medical School (US)
- Centre National de la Recherche Scientifique (FR)
- Inserm (FR)
- Humboldt-Universität zu Berlin (DE)
- University of California, San Francisco (US)
- Erasmus MC (NL)
- Corresponding author
- Dekker, Job
- ORCID
- Venue
- Nature
- Published
- 2012-04-11
- Volume
- 485
- Issue
- 7398
- Pages
- 381-385
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC3555144
- OpenAlex
- W2161212572
- Cited by
- 2,895
- References
- 32
- Citations by year
- 2026: 145 · 2025: 168 · 2024: 181 · 2023: 213 · 2022: 241 · 2021: 276 · 2020: 255 · 2019: 300 · 2018: 247 · 2017: 241 · 2016: 201 · 2015: 173 · 2014: 112 · 2013: 103 · 2012: 34
- FWCI
- 50.79
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (publishedVersion)
- PubMed Central (acceptedVersion)
- MPG.PuRe (Max Planck Society) (submittedVersion, other-oa)
- The Journal of the American Medical Association (JAMA) Network (American Medical Association) (submittedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (submittedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Max Planck Digital Library (submittedVersion, other-oa)
- Funders
- W. M. Keck Foundation
- European Commission (257082, 242129)
- Agence Nationale de la Recherche (ANR-10-INBS-0009)
- Bundesministerium für Bildung und Forschung
- National Institutes of Health
- National Human Genome Research Institute (R01HG003143)
- FP7 Ideas: European Research Council (250367)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Chromosomal and Genetic Variations
- Keywords
- X inactivation center, XIST, Tsix, topologically associating domains, 3D genome organization, long-range transcriptional regulation, X chromosome inactivation, chromatin interactions, embryonic stem cells, cell differentiation, lamina-associated domains, distal regulatory regions
- MeSH terms
- Animals, Cell Differentiation, Female, Fibroblasts, Gene Expression Regulation, Histones, Male, Methylation, Molecular Sequence Data, Promoter Regions, Genetic, X Chromosome, In Situ Hybridization, Fluorescence, DNA, Intergenic, RNA, Untranslated, Epigenesis, Genetic, X Chromosome Inactivation, Mice, Embryonic Stem Cells, Epigenomics, Transcriptome, RNA, Long Noncoding
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