The DOI matches its Crossref record; 109 of the 109 references it cites were found in a registry or an index.
Higher-Order Inter-chromosomal Hubs Shape 3D Genome Organization in the Nucleus
Open accessPublished version of a preprint
Abstract
Eukaryotic genomes are packaged into a 3-dimensional structure in the nucleus. Current methods for studying genome-wide structure are based on proximity ligation. However, this approach can fail to detect known structures, such as interactions with nuclear bodies, because these DNA regions can be too far apart to directly ligate. Accordingly, our overall understanding of genome organization remains incomplete. Here, we develop split-pool recognition of interactions by tag extension (SPRITE), a method that enables genome-wide detection of higher-order interactions within the nucleus. Using SPRITE, we recapitulate known structures identified by proximity ligation and identify additional interactions occurring across larger distances, including two hubs of inter-chromosomal interactions that are arranged around the nucleolus and nuclear speckles. We show that a substantial fraction of the genome exhibits preferential organization relative to these nuclear bodies. Our results generate a global model whereby nuclear bodies act as inter-chromosomal hubs that shape the overall packaging of DNA in the nucleus.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“While both methods could successfully reveal multi-way contacts across TADs and chromosomes, their resolution currently limits robust detection of individual CRUs.”
From Transcriptional enhancers and their communication with gene promoters (2021) · cites this paper as [403]
Experimental — accuracy not yet measuredIn the citing paper
“In the last decade, proximity ligation methods have played an important role in identifying these key interactions, such as promoter and enhancer associations (Kempfer and Pombo, 2020; Oudelaar et al., 2018; Quinodoz et al., 2018).”
From Unraveling Hematopoiesis through the Lens of Genomics (2020) · cites this paper as Quinodoz et al., 2018
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
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
Master Transcription Factors and Mediator Establish Super-Enhancers at Key Cell Identity Genes
Whyte, W. A., Orlando, D. A., Hnisz, D., Abraham, B. J., Lin, C. Y., Kagey, M. H., Rahl, P. B., Lee, T. I., & Young, R. A. (2013) · Cell · doi:10.1016/j.cell.2013.03.035 · Cited by 4,143
Capturing Chromosome Conformation
Dekker, J., Rippe, K., Dekker, M., & Kleckner, N. (2002) · Science · doi:10.1126/science.1067799 · Cited by 3,652
Spatial partitioning of the regulatory landscape of the X-inactivation centre
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., et al. (2012) · Nature · doi:10.1038/nature11049 · Cited by 2,895
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
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
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
Boisvert, F., van Koningsbruggen, S., de Navascués, J., & Lamond, A. I. (2007) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm2184 · Cited by 1,671
Chromatin architecture reorganization during stem cell differentiation
Dixon, J. R., Jung, I., Selvaraj, S., Shen, Y., Antosiewicz-Bourget, J. E., Lee, A. Y., Ye, Z., Kim, A., Rajagopal, N., Xie, W., et al. (2015) · Nature · doi:10.1038/nature14222 · Cited by 1,646
Chromosome TerritoriesPreprint
Cremer, T. J., & Cremer, M. (2010) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a003889 · Cited by 1,195
Architectural protein subclasses shape 3D organization of genomes during lineage commitment
Phillips-Cremins, J. E., Sauria, M. E. G., Sanyal, A., Gerasimova, T. I., Lajoie, B. R., Bell, J. S. K., Ong, C.-T., Hookway, T. A., Guo, C., Sun, Y., et al. (2013) · Cell · doi:10.1016/j.cell.2013.04.053 · Cited by 1,187
Lichter, P., Cremer, T., Borden, J., Manuelidis, L., & Ward, D. C. (1988) · Human Genetics · doi:10.1007/bf01790090 · Cited by 1,160
Charting histone modifications and the functional organization of mammalian genomes
Zhou, V. W., Goren, A., & Bernstein, B. E. (2011) · Nature Reviews Genetics · doi:10.1038/nrg2905 · Cited by 1,147
The Xist lncRNA interacts directly with SHARP to silence transcription through HDAC3
McHugh, C. A., Chen, C., Chow, A. Y., Surka, C., Tran, C., McDonel, P. E., Pandya‐Jones, A., Blanco, M. R., Burghard, C. P., Moradian, A., et al. (2015) · Nature · doi:10.1038/nature14443 · Cited by 1,139
HiChIP: efficient and sensitive analysis of protein-directed genome architecture
Mumbach, M. R., Rubin, A. J., Flynn, R. A., Dai, C., Khavari, P. A., Greenleaf, W. J., & Chang, H. Y. (2016) · Nature Methods · doi:10.1038/nmeth.3999 · Cited by 1,139
Molecular 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
Hutchinson, J. N., Ensminger, A. W., Clemson, C., Lynch, C. R., Lawrence, J. B., & Chess, A. J. (2007) · BMC Genomics · doi:10.1186/1471-2164-8-39 · Cited by 1,017
The Xist lncRNA Exploits Three-Dimensional Genome Architecture to Spread Across the X Chromosome
Engreitz, J., Pandya‐Jones, A., McDonel, P. E., Shishkin, A., Sirokman, K., Surka, C., Kadri, S., Xing, J. C., Goren, A., Lander, E. S., et al. (2013) · Science · doi:10.1126/science.1237973 · Cited by 1,008
Super-resolution imaging reveals distinct chromatin folding for different epigenetic states
Boettiger, A. N., Bintu, B., Moffitt, J. R., Wang, S., Beliveau, B. J., Fudenberg, G., Imakaev, M., Mirny, L. A., Wu, C.-T., & Zhuang, X. (2016) · Nature · doi:10.1038/nature16496 · Cited by 871
Nuclear SpecklesPreprint
Spector, D. L., & Lamond, A. I. (2010) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a000646 · Cited by 842
P-Bodies and Stress Granules: Possible Roles in the Control of Translation and mRNA DegradationPreprint
Decker, C. J., & Parker, R. (2012) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a012286 · Cited by 806
A long nuclear‐retained non‐coding RNA regulates synaptogenesis by modulating gene expression
Bernard, D., Prasanth, K. V., Tripathi, V., Colasse, S., Nakamura, T., Xuan, Z., Zhang, M. Q., Sedel, F., Jourdren, L., Coulpier, F., et al. (2010) · The EMBO Journal · doi:10.1038/emboj.2010.199 · Cited by 750
Interchromosomal associations between alternatively expressed loci
Spilianakis, C. G., Lalioti, M. D., Town, T., Lee, G. R., & Flavell, R. A. (2005) · Nature · doi:10.1038/nature03574 · Cited by 742
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
The Hierarchy of the 3D Genome
Gibcus, J. H., & Dekker, J. (2013) · Molecular Cell · doi:10.1016/j.molcel.2013.02.011 · Cited by 727
Complex multi-enhancer contacts captured by genome architecture mapping
Beagrie, R. A., Scialdone, A., Schueler, M., Kraemer, D. C. A., Chotalia, M., Xie, S. Q., Barbieri, M., de Santiago, I., Lavitas, L.-M., Branco, M. R., et al. (2017) · Nature · doi:10.1038/nature21411 · Cited by 715
Branco, M. R., & Pombo, A. (2006) · PLoS Biology · doi:10.1371/journal.pbio.0040138 · Cited by 685
RNA motif discovery by SHAPE and mutational profiling (SHAPE-MaP)
Siegfried, N. A., Busan, S., Rice, G. M., Nelson, J. A. E., & Weeks, K. M. (2014) · Nature Methods · doi:10.1038/nmeth.3029 · Cited by 675
Topological organization of multichromosomal regions by the long intergenic noncoding RNA Firre
Hacisuleyman, E., Goff, L. A., Trapnell, C., Williams, A., Henao‐Mejia, J., Sun, L., McClanahan, P. D., Hendrickson, D. G., Sauvageau, M., Kelley, D. R., et al. (2014) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.2764 · Cited by 644
Interchromosomal Interactions and Olfactory Receptor Choice
Lomvardas, S., Barnea, G., Pisapia, D. J., Mendelsohn, M. M., Kirkland, J., & Axel, R. (2006) · Cell · doi:10.1016/j.cell.2006.06.035 · Cited by 641
Spatial organization of chromatin domains and compartments in single chromosomes
Wang, S., Su, J.-H., Beliveau, B. J., Bintu, B., Moffitt, J. R., Wu, C.-T., & Zhuang, X. (2016) · Science · doi:10.1126/science.aaf8084 · Cited by 617
Three-dimensional genome architecture: players and mechanisms
Pombo, A., & Dillon, N. (2015) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3965 · Cited by 603
Jonkers, I., Kwak, H., & Lis, J. T. (2014) · eLife · doi:10.7554/elife.02407 · Cited by 581
PML Nuclear BodiesPreprint
Lallemand-Breitenbach, V., & de Thé, H. (2010) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a000661 · Cited by 561
Massively multiplex single-cell Hi-C
Ramani, V., Deng, X., Qiu, R., Gunderson, K. L., Steemers, F. J., Distèche, C. M., Noble, W. S., Duan, Z., & Shendure, J. (2017) · Nature Methods · doi:10.1038/nmeth.4155 · Cited by 545
Engreitz, J., Sirokman, K., McDonel, P. E., Shishkin, A. A., Surka, C., Russell, P. H., Grossman, S. R., Chow, A. Y., Guttman, M., & Lander, E. S. (2014) · Cell · doi:10.1016/j.cell.2014.08.018 · Cited by 514
The Human and Mouse Replication-Dependent Histone Genes
Marzluff, W. F., Gongidi, P., Woods, K., Jin, J., & Maltais, L. J. (2002) · Genomics · doi:10.1006/geno.2002.6850 · Cited by 489
Meuleman, W., Peric-Hupkes, D., Kind, J., Beaudry, J.-B., Pagie, L., Kellis, M., Reinders, M., Wessels, L., & van Steensel, B. (2013) · Genome Research · doi:10.1101/gr.141028.112 · Cited by 462
Pederson, T. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a000638 · Cited by 455
CTCF Mediates Interchromosomal Colocalization Between Igf2/H19 and Wsb1/Nf1
Ling, J. Q., Li, T., Hu, J., Vu, T. H., Chen, H. L., Qiu, X. W., Cherry, A. M., & Hoffman, A. R. (2006) · Science · doi:10.1126/science.1123191 · Cited by 437
The Role of Chromosome Domains in Shaping the Functional Genome
Sexton, T., & Cavalli, G. (2015) · Cell · doi:10.1016/j.cell.2015.02.040 · Cited by 427
Functional implications of genome topology
Cavalli, G., & Misteli, T. (2013) · Nature Structural & Molecular Biology · doi:10.1038/nsmb.2474 · Cited by 415
Initial Genomics of the Human Nucleolus
Németh, A., Conesa, A., Santoyo‐López, J., Medina, I., Montaner, D. A., Péterfia, B. F., Solovei, I. V., Cremer, T. J., Dopazo, J., & Längst, G. (2010) · PLoS Genetics · doi:10.1371/journal.pgen.1000889 · Cited by 399
The 3D genome in transcriptional regulation and pluripotency
Gorkin, D. U., Leung, D., & Ren, B. (2014) · Cell Stem Cell · doi:10.1016/j.stem.2014.05.017 · Cited by 391
Meaburn, K. J., & Misteli, T. (2007) · Nature · doi:10.1038/445379a · Cited by 367
Golgi Bypass: Skirting Around the Heart of Classical SecretionPreprint
Grieve, A. G., & Rabouille, C. (2011) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a005298 · Cited by 355
Highly multiplexed simultaneous detection of RNAs and proteins in single cells
Frei, A. P., Bava, F.-A., Zunder, E. R., Hsieh, E. W. Y., Chen, S.-Y., Nolan, G. P., & Gherardini, P. F. (2016) · Nature Methods · doi:10.1038/nmeth.3742 · Cited by 330
Long noncoding RNAs: an emerging link between gene regulation and nuclear organization
Quinodoz, S. A., & Guttman, M. (2014) · Trends in Cell Biology · doi:10.1016/j.tcb.2014.08.009 · Cited by 327
RNA Polymerase II Targets Pre-mRNA Splicing Factors to Transcription Sites In Vivo
Misteli, T., & Spector, D. L. (1999) · Molecular Cell · doi:10.1016/s1097-2765(01)80002-2 · Cited by 326
IP3 Receptors: Toward Understanding Their ActivationPreprint
Taylor, C. W., & Tovey, S. C. (2010) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a004010 · Cited by 304
Mahy, N. L., Perry, P. E., & Bickmore, W. A. (2002) · The Journal of Cell Biology · doi:10.1083/jcb.200207115 · Cited by 302
Simultaneous generation of many RNA-seq libraries in a single reaction
Shishkin, A. A., Giannoukos, G., Küçükural, A., Ciulla, D., Busby, M., Surka, C., Chen, J., Bhattacharyya, R. P., Rudy, R. F., Patel, M. M., et al. (2015) · Nature Methods · doi:10.1038/nmeth.3313 · Cited by 288
The DNA sequence and analysis of human chromosome 6
Mungall, A. J. J., Palmer, S., Sims, S. K., Edwards, C. A., Ashurst, J. L., Wilming, L. G., Jones, M. C., Horton, R., Hunt, S. E., Scott, C., et al. (2003) · Nature · doi:10.1038/nature02055 · Cited by 287
Brown, J. M., Green, J., das Neves, R. P., Wallace, H. A. C., Smith, A. J. H., Hughes, J. R., Gray, N., Taylor, S., Wood, W. G., Higgs, D. R., et al. (2008) · The Journal of Cell Biology · doi:10.1083/jcb.200803174 · Cited by 285
Blecher‐Gonen, R., Barnett‐Itzhaki, Z., Jaitin, D. A., Amann‐Zalcenstein, D., Lara‐Astiaso, D., & Amit, I. (2013) · Nature Protocols · doi:10.1038/nprot.2013.023 · Cited by 281
The Cajal Body and Histone Locus BodyPreprint
Nizami, Z. F., Deryusheva, S., & Gall, J. G. (2010) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a000653 · Cited by 276
Deletion of DXZ4 on the human inactive X chromosome alters higher-order genome architecture
Darrow, E. M., Huntley, M. H., Dudchenko, O., Stamenova, E. K., Durand, N. C., Sun, Z., Huang, S.-C., Sanborn, A. L., Machol, I., Shamim, M., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1609643113 · Cited by 276
Biogenesis of Nuclear BodiesPreprint
Dundr, M., & Misteli, T. (2010) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a000711 · Cited by 274
Nucleolar organizer regions: genomic ‘dark matter’ requiring illuminationPreprint
McStay, B. (2016) · Genes & Development · doi:10.1101/gad.283838.116 · Cited by 264
Xist recruits the X chromosome to the nuclear lamina to enable chromosome-wide silencing
Chen, C., Blanco, M. R., Jackson, C., Aznauryan, E. I., Ollikainen, N., Surka, C., Chow, A. Y., Cerase, A., McDonel, P. E., & Guttman, M. (2016) · Science · doi:10.1126/science.aae0047 · Cited by 262
Williamson, I., Berlivet, S., Eskeland, R., Boyle, S., Illingworth, R. S., Paquette, D., Dostie, J., & Bickmore, W. A. (2014) · Genes & Development · doi:10.1101/gad.251694.114 · Cited by 239
Miyagawa, R., Tano, K., Mizuno, R., Nakamura, Y., Ijiri, K., Rakwal, R., Shibato, J., Masuo, Y., Mayeda, A., Hirose, T., et al. (2012) · RNA · doi:10.1261/rna.028639.111 · Cited by 237
An Overview of Genome Organization and How We Got There: from FISH to Hi-C
Fraser, J., Williamson, I., Bickmore, W. A., & Dostie, J. (2015) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.00006-15 · Cited by 232
Genome organization in and around the nucleolus
Németh, A., & Längst, G. (2011) · Trends in Genetics · doi:10.1016/j.tig.2011.01.002 · Cited by 216
Clustering of multiple specific genes and gene-rich R-bands around SC-35 domains
Shopland, L. S., Johnson, C. V., Byron, M., McNeil, J. A., & Lawrence, J. B. (2003) · The Journal of Cell Biology · doi:10.1083/jcb.200303131 · Cited by 209
Concerted copy number variation balances ribosomal DNA dosage in human and mouse genomes
Gibbons, J. G., Branco, A. T., Godinho, S. A., Yu, S., & Lemos, B. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1416878112 · Cited by 201
Erratum: Organization and function of the 3D genome
Bonev, B., & Cavalli, G. (2016) · Nature Reviews Genetics · doi:10.1038/nrg.2016.147 · Cited by 184
Cajal bodies and coilin—moving towards function
Ogg, S. C., & Lamond, A. I. (2002) · The Journal of Cell Biology · doi:10.1083/jcb.200206111 · Cited by 182
Population-based 3D genome structure analysis reveals driving forces in spatial genome organization
Tjong, H., Li, W., Kalhor, R., Dai, C., Hao, S., Gong, K. Q., Zhou, Y., Li, H., Zhou, X. J., Gros, M. A. L., et al. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1512577113 · Cited by 181
Nucleolus and nuclear periphery: Velcro for heterochromatin
Padeken, J., & Heun, P. (2014) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2014.03.001 · Cited by 179
Kruhlak, M. J., Lever, M. A., Fischle, W., Verdin, E. M., Bazett‐Jones, D. P., & Hendzel, M. J. (2000) · The Journal of Cell Biology · doi:10.1083/jcb.150.1.41 · Cited by 174
HSP70 Transgene Directed Motion to Nuclear Speckles Facilitates Heat Shock Activation
Khanna, N., Hu, Y., & Belmont, A. S. (2014) · Current Biology · doi:10.1016/j.cub.2014.03.053 · Cited by 170
Chromosome crosstalk in three dimensions
Göndör, A., & OHLSSON, R. I. (2009) · Nature · doi:10.1038/nature08453 · Cited by 152
“Cat’s Cradling” the 3D Genome by the Act of LncRNA Transcription
Melé, M., & Rinn, J. L. (2016) · Molecular Cell · doi:10.1016/j.molcel.2016.05.011 · Cited by 152
U1 and U2 small nuclear RNAs are present in nuclear speckles.
Huang, S., & Spector, D. L. (1992) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.89.1.305 · Cited by 149
Capturing pairwise and multi-way chromosomal conformations using chromosomal walks
Olivares‐Chauvet, P., Mukamel, Z., Lifshitz, A., Schwartzman, O., Elkayam, N. O., Lubling, Y., Deikus, G. Y., Sebra, R., & Tanay, A. (2016) · Nature · doi:10.1038/nature20158 · Cited by 141
FISH-ing for captured contacts: towards reconciling FISH and 3C
Fudenberg, G., & Imakaev, M. (2017) · Nature Methods · doi:10.1038/nmeth.4329 · Cited by 141
Immuno-PCR: An ultrasensitive immunoassay for biomolecular detection
Chang, L., Li, J., & Wang, L. (2016) · Analytica Chimica Acta · doi:10.1016/j.aca.2015.12.039 · Cited by 139
Closing the loop: 3C versus DNA FISH
Giorgetti, L., & Heard, E. (2016) · Genome Biology · doi:10.1186/s13059-016-1081-2 · Cited by 131
RNA and dynamic nuclear organization
Rinn, J. L., & Guttman, M. (2014) · Science · doi:10.1126/science.1252966 · Cited by 129
Molenaar, C., Abdulle, A., Gena, A., Tanke, H. J., & Dirks, R. W. (2004) · The Journal of Cell Biology · doi:10.1083/jcb.200310139 · Cited by 125
Rajapakse, I., & Groudine, M. T. (2011) · The Journal of Cell Biology · doi:10.1083/jcb.201010129 · Cited by 123
NUCLEOLUS ORGANIZERS IN MUS MUSCULUS SUBSPECIES AND IN THE RAG MOUSE CELL LINE
Dev, V. G., Tantravahi, R. V., Miller, D. A., & Miller, O. J. (1977) · Genetics · doi:10.1093/genetics/86.2.389 · Cited by 115
Gheldof, N., Smith, E. M., Tabuchi, T. M., Koch, C. M., Dunham, I., Stamatoyannopoulos, J. A., & Dekker, J. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq175 · Cited by 114
Newport, J. W., & Dunphy, W. G. (1992) · The Journal of Cell Biology · doi:10.1083/jcb.116.2.295 · Cited by 109
The Coilin Interactome Identifies Hundreds of Small Noncoding RNAs that Traffic through Cajal Bodies
Machyna, M., Kehr, S., Straube, K., Kappei, D., Buchholz, F., Butter, F., Ule, J., Jana Hertel, A., Stadler, P. F., & Neugebauer, K. M. (2014) · Molecular Cell · doi:10.1016/j.molcel.2014.10.004 · Cited by 107
The Nucleoplasmin Homolog NLP Mediates Centromere Clustering and Anchoring to the Nucleolus
Padeken, J., Mendiburo, M. J., Chlamydas, S., Schwarz, H.-J., Kremmer, E., & Heun, P. (2013) · Molecular Cell · doi:10.1016/j.molcel.2013.03.002 · Cited by 100
ChIA-PET analysis of transcriptional chromatin interactions
Zhang, J., Poh, H. M., Peh, S. Q., Sia, Y. Y., Li, G., Mulawadi, F. H., Goh, Y., Fullwood, M. J., Sung, W.-K. K., Ruan, X., et al. (2012) · Methods · doi:10.1016/j.ymeth.2012.08.009 · Cited by 96
Formation of nuclear heterochromatin
Guetg, C., & Santoro, R. (2012) · Epigenetics · doi:10.4161/epi.21072 · Cited by 96
The Human and Mouse Replication-Dependent Histone Genes
Marzluff, W. F., Gongidi, P., Woods, K., et al. (2002) · Genomics · doi:10.1016/s0888-7543(02)96850-3 · Cited by 91
3C-based technologies to study the shape of the genome
de Laat, W., & Dekker, J. (2012) · Methods · doi:10.1016/j.ymeth.2012.11.005 · Cited by 84
Multiplexed Dynamic Imaging of Genomic Loci by Combined CRISPR Imaging and DNA Sequential FISH
Takei, Y., Shah, S., Harvey, S. C., Qi, L. S., & Cai, L. (2017) · Biophysical Journal · doi:10.1016/j.bpj.2017.03.024 · Cited by 84
Structure and Epigenetics of Nucleoli in Comparison With Non-nucleolar Compartments
Bártová, E., Horáková, A. H., Uhlířová, R., Raška, I., Galiová, G., Orlova, D. Y., & Kozubek, S. (2009) · Journal of Histochemistry & Cytochemistry · doi:10.1369/jhc.2009.955435 · Cited by 71
Hi-Corrector: a fast, scalable and memory-efficient package for normalizing large-scale Hi-C data
Li, W., Gong, K. Q., Li, Q., Alber, F., & Zhou, X. J. (2014) · Bioinformatics · doi:10.1093/bioinformatics/btu747 · Cited by 71
The Perinucleolar CompartmentPreprint
Pollock, C. B., & Huang, S. (2010) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a000679 · Cited by 67
Chromosome intermingling—the physical basis of chromosome organization in differentiated cells
Maharana, S., Iyer, K. V., Jain, N., Nagarajan, M., Wang, Y., & Shivashankar, G. V. (2016) · Nucleic Acids Research · doi:10.1093/nar/gkw131 · Cited by 66
Britton-Davidian, J., Cazaux, B., & Catalan, J. (2012) · Heredity · doi:10.1038/hdy.2011.105 · Cited by 65
Suzuki, H., Kurihara, Y., Kanehisa, T., & Moriwaki, K. (1990) · Molecular Biology and Evolution · doi:10.1093/oxfordjournals.molbev.a040598 · Cited by 64
Mapping the 3D genome: Aiming for consilience
Dekker, J. (2016) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm.2016.151 · Cited by 58
Hsp70 gene association with nuclear speckles is Hsp70 promoter specific
Hu, Y., Plutz, M., & Belmont, A. S. (2010) · The Journal of Cell Biology · doi:10.1083/jcb.201004041 · Cited by 57
The statistical-mechanics of chromosome conformation capture
O'Sullivan, J. M., Hendy, M. D., Pichugina, T., Wake, G. C., & Langowski, J. (2013) · Nucleus · doi:10.4161/nucl.26513 · Cited by 54
Chromosomal locations of Ag-NORs and clusters of ribosomal DNA in laboratory strains of mice
Kurihara, Y., Suh, D., Suzuki, H., & Moriwaki, K. (1994) · Mammalian Genome · doi:10.1007/bf00360550 · Cited by 43
Gene associations: true romance or chance meeting in a nuclear neighborhood?
Lawrence, J. B., & Clemson, C. (2008) · The Journal of Cell Biology · doi:10.1083/jcb.200808121 · Cited by 37
Pollock, C. B., & Huang, S. (2009) · Journal of Cellular Biochemistry · doi:10.1002/jcb.22107 · Cited by 31
Nucleolar tethering mediates pairing between theIgHandMycloci
Strongin, D. E., Groudine, M. T., & Politz, J. C. R. (2014) · Nucleus · doi:10.4161/nucl.36233 · Cited by 17
Heterogeneity and Intrinsic Variation in Spatial Genome OrganizationPreprint
Finn, E. H., Pegoraro, G., Brandão, H. B., Valton, A.-L., Oomen, M. E., Dekker, J., Mirny, L. A., & Misteli, T. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/171801 · Cited by 14
Centromeres in nuclear architecture
Padeken, J., & Heun, P. (2013) · Cell Cycle · doi:10.4161/cc.26697 · Cited by 7
Flagged first, then by citations
Cited by
Sorted by citations
Super-resolution chromatin tracing reveals domains and cooperative interactions in single cells
Bintu, B., Mateo, L. J., Su, J.-H., Sinnott-Armstrong, N. A., Parker, M., Kinrot, S., Yamaya, K., Boettiger, A. N., & Zhuang, X. (2018) · Science · doi:10.1126/science.aau1783 · Cited by 976
The role of 3D genome organization in development and cell differentiation
Zheng, H., & Xie, W. (2019) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-019-0132-4 · Cited by 742
The Self-Organizing Genome: Principles of Genome Architecture and Function
Misteli, T. (2020) · Cell · doi:10.1016/j.cell.2020.09.014 · Cited by 742
Liquid Nuclear Condensates Mechanically Sense and Restructure the Genome
Shin, Y., Chang, Y.-C., Lee, D. S. W., Berry, J., Sanders, D. W., Ronceray, P., Wingreen, N. S., Haataja, M., & Brangwynne, C. P. (2018) · Cell · doi:10.1016/j.cell.2018.10.057 · Cited by 676
Pol II phosphorylation regulates a switch between transcriptional and splicing condensates
Guo, Y. E., Manteiga, J. C., Henninger, J. E., Sabari, B. R., Dall’Agnese, A., Hannett, N. M., Spille, J.-H., Afeyan, L. K., Zamudio, A. V., Shrinivas, K., et al. (2019) · Nature · doi:10.1038/s41586-019-1464-0 · Cited by 674
Metadata
- Authors
- Quinodoz, S. A., Ollikainen, N., Tabak, B., Palla, A., Schmidt, J. M., Detmar, E., Lai, M. M., Shishkin, A. A., Bhat, P., Takei, Y., Trinh, V., Aznauryan, E., Russell, P., Cheng, C., Jovanovic, M., Chow, A., Cai, L., McDonel, P., Garber, M., & Guttman, M.
- Affiliations
- California Institute of Technology (US)
- University of Massachusetts Chan Medical School (US)
- Colorado School of Public Health (US)
- Boston University (US)
- Corresponding author
- Guttman, Mitchell
- ORCID
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2018-07
- Volume
- 174
- Issue
- 3
- Pages
- 744-757.e24
- ISSN
- 0092-8674 (ISSN-L)
- PMC
- PMC6548320
- OpenAlex
- W2806123558
- Cited by
- 892
- References
- 108
- Citations by year
- 2026: 78 · 2025: 101 · 2024: 107 · 2023: 115 · 2022: 118 · 2021: 131 · 2020: 112 · 2019: 100 · 2018: 28
- FWCI
- 33.35
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell (publishedVersion)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- CaltechAUTHORS (California Institute of Technology) (submittedVersion)
- The Journal of the American Medical Association (JAMA) Network (American Medical Association) (submittedVersion)
- Funders
- HHMI Gilliam Fellowship
- NSF GRFP Fellowship
- NIGMS (T32 GM008042)
- UCLA-Caltech MSTP (NIGMS T32 GM008042)
- NIH 4DN Program (U01 DA040612, U01 HL130007)
- NHGRI GGR Program (U01 HG007910)
- New York Stem Cell Foundation (NYSCF-R-I13)
- Sontag Foundation
- Caltech
- 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 › Genetics › Chromosomal and Genetic Variations
- Keywords
- 3D genome organization, interchromosomal interactions, nuclear bodies, nucleolus, nuclear speckles, sprites, long-range chromatin interactions, DNA packaging
- MeSH terms
- Cell Nucleolus, Cell Nucleus, Chromosome Mapping, Chromosomes, DNA, Humans, Structure-Activity Relationship, Genome, Eukaryota
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review