The DOI matches its Crossref record; 62 of the 63 references it cites were found in a registry or an index.
The genomic landscape of cohesin-associated chromatin interactions
Open accessAbstract
Cohesin is implicated in establishing tissue-specific DNA loops that target enhancers to promoters, and also localizes to sites bound by the insulator protein CTCF, which blocks enhancer-promoter communication. However, cohesin-associated interactions have not been characterized on a genome-wide scale. Here we performed chromatin interaction analysis with paired-end tag sequencing (ChIA-PET) of the cohesin subunit SMC1A in developing mouse limb. We identified 2264 SMC1A interactions, of which 1491 (65%) involved sites co-occupied by CTCF. SMC1A participates in tissue-specific enhancer-promoter interactions and interactions that demarcate regions of correlated regulatory output. In contrast to previous studies, we also identified interactions between promoters and distal sites that are maintained in multiple tissues but are poised in embryonic stem cells and resolve to tissue-specific activated or repressed chromatin states in the mouse embryo. Our results reveal the diversity of cohesin-associated interactions in the genome and highlight their role in establishing the regulatory architecture of development.
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?
In the citing paper
“Enhancer-bound proteins are constrained such that they tend to interact only with genes within these CTCF-CTCF loops.”
From Insulated Neighborhoods: Structural and Functional Units of Mammalian Gene Control (2016) · cites this paper as DeMare et al., 2013
In the citing paper
“In the models that emerge from these data, each chromosome contains thousands of DNA loops, formed by the interaction of two CTCF molecules bound to different sites, and reinforced by a cohesin molecule (Figure 2A).”
From Insulated Neighborhoods: Structural and Functional Units of Mammalian Gene Control (2016) · cites this paper as DeMare et al., 2013
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
The Sequence Alignment/Map format and SAMtools
Li, H., Handsaker, B., Wysoker, A., Fennell, T., Ruan, J., Homer, N., Marth, G., Abecasis, G., Durbin, R., & 1000 Genome Project Data Processing Subgroup (2009) · Bioinformatics · doi:10.1093/bioinformatics/btp352 · Cited by 62,041
Cutadapt removes adapter sequences from high-throughput sequencing reads
Martin, M. (2011) · EMBnet.journal · doi:10.14806/ej.17.1.200 · Cited by 33,889
BEDTools: a flexible suite of utilities for comparing genomic features
Quinlan, A. R., & Hall, I. M. (2010) · Bioinformatics · doi:10.1093/bioinformatics/btq033 · Cited by 27,437
Ultrafast and memory-efficient alignment of short DNA sequences to the human genome.
Langmead, B., Trapnell, C., Pop, M., & Salzberg, S. L. (2009) · Genome Biology · doi:10.1186/gb-2009-10-3-r25 · Cited by 21,849
Model-based Analysis of ChIP-Seq (MACS)
Zhang, Y., Liu, T., Meyer, C. A., Eeckhoute, J., Johnson, D. S., Bernstein, B. E., Nusbaum, C., Myers, R. M., Brown, M., Li, W., et al. (2008) · Genome Biology · doi:10.1186/gb-2008-9-9-r137 · Cited by 18,386
Mapping and quantifying mammalian transcriptomes by RNA-Seq
Mortazavi, A., Williams, B. A., McCue, K., Schaeffer, L., & Wold, B. (2008) · Nature Methods · doi:10.1038/nmeth.1226 · Cited by 13,696
Gene Expression Omnibus: NCBI gene expression and hybridization array data repository
Edgar, R. (2002) · Nucleic Acids Research · doi:10.1093/nar/30.1.207 · Cited by 13,288
TopHat: discovering splice junctions with RNA-Seq
Trapnell, C., Pachter, L. S., & Salzberg, S. L. (2009) · Bioinformatics · doi:10.1093/bioinformatics/btp120 · Cited by 11,682
Circos: An information aesthetic for comparative genomicsPreprint
Krzywinski, M. I., Schein, J. E., Birol, İ., Connors, J. M., Gascoyne, R. D., Horsman, D. E., Jones, S. J. M., & Marra, M. A. (2009) · Genome Research · doi:10.1101/gr.092759.109 · Cited by 11,073
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
Flagged first, then by citations
1 of the 63 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
CTCF: an architectural protein bridging genome topology and function
Ong, C., & Corces, V. G. (2014) · Nature Reviews Genetics · doi:10.1038/nrg3663 · Cited by 1,088
Control of cell identity genes occurs in insulated neighborhoods in mammalian chromosomes
Dowen, J. M., Fan, Z. P., Hnisz, D., Ren, G., Abraham, B. J., Zhang, L. N., Weintraub, A. S., Schuijers, J., Lee, T. I., Zhao, K., et al. (2014) · Cell · doi:10.1016/j.cell.2014.09.030 · Cited by 884
Rivera, C. M., & Ren, B. (2013) · Cell · doi:10.1016/j.cell.2013.09.011 · Cited by 550
Functional and topological characteristics of mammalian regulatory domains
Symmons, O., Uslu, V. V., Tsujimura, T., Ruf, S., Nassari, S., Schwarzer, W., Ettwiller, L., & Spitz, F. (2014) · Genome Research · doi:10.1101/gr.163519.113 · Cited by 455
Insulated Neighborhoods: Structural and Functional Units of Mammalian Gene Control
Hnisz, D., Day, D. S., & Young, R. A. (2016) · Cell · doi:10.1016/j.cell.2016.10.024 · Cited by 420
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
3D Chromosome Regulatory Landscape of Human Pluripotent Cells
Ji, X., Dadon, D. B., Powell, B. E., Fan, Z. P., Borges-Rivera, D., Shachar, S., Weintraub, A. S., Hnisz, D., Pegoraro, G., Lee, T. I., et al. (2016) · Cell Stem Cell · doi:10.1016/j.stem.2015.11.007 · Cited by 400
Cohesin-mediated interactions organize chromosomal domain architecture
Sofueva, S., Yaffe, E., Chan, W., Georgopoulou, D., Vietri Rudan, M., Mira‐Bontenbal, H., Pollard, S. M., Schroth, G. P., Tanay, A., & Hadjur, S. (2013) · The EMBO Journal · doi:10.1038/emboj.2013.237 · Cited by 394
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
An atlas of dynamic chromatin landscapes in mouse fetal development
Gorkin, D. U., Barozzi, I., Zhao, Y., Zhang, Y., Huang, H., Lee, A. Y., Li, B., Chiou, J., Wildberg, A., Ding, B., et al. (2020) · Nature · doi:10.1038/s41586-020-2093-3 · Cited by 374
Wapl is an essential regulator of chromatin structure and chromosome segregation
Tedeschi, A., Wutz, G., Huet, S., Jaritz, M., Wuensche, A., Schirghuber, E., Davidson, I. F., Tang, W., Cisneros, D. A., Bhaskara, V., et al. (2013) · Nature · doi:10.1038/nature12471 · Cited by 359
Li, L., Lyu, X., Hou, C., Takenaka, N., Nguyen, H. Q., Ong, C., Cubeñas-Potts, C., Hu, M., Lei, E. P., Bosco, G., et al. (2015) · Molecular Cell · doi:10.1016/j.molcel.2015.02.023 · Cited by 315
Genome-wide map of regulatory interactions in the human genome
Heidari, N., Phanstiel, D. H., He, C., Grubert, F., Jahanbani, F., Kasowski, M., Zhang, M. Q., & Snyder, M. P. (2014) · Genome Research · doi:10.1101/gr.176586.114 · Cited by 278
Global view of enhancer–promoter interactome in human cells
He, B., Chen, C., Teng, L., & Tan, K. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1320308111 · Cited by 263
A tiling-deletion-based genetic screen for cis-regulatory element identification in mammalian cells
Diao, Y., Fang, R., Li, B., Meng, Z., Yu, J., Qiu, Y., Lin, K. C., Huang, H., Liu, T., Marina, R. J., et al. (2017) · Nature Methods · doi:10.1038/nmeth.4264 · Cited by 259
Limb development: a paradigm of gene regulation
Petit, F., Sears, K. E., & Ahituv, N. (2017) · Nature Reviews Genetics · doi:10.1038/nrg.2016.167 · Cited by 198
Ron, G., Globerson, Y., Moran, D., & Kaplan, T. (2017) · Nature Communications · doi:10.1038/s41467-017-02386-3 · Cited by 188
Clustering of Tissue-Specific Sub-TADs Accompanies the Regulation of HoxA Genes in Developing Limbs
Berlivet, S., Paquette, D., Dumouchel, A., Langlais, D., Dostie, J., & Kmita, M. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1004018 · Cited by 170
Locus-Specific Targeting to the X Chromosome Revealed by the RNA Interactome of CTCF
Kung, J. T., Kesner, B., An, J. Y., Ahn, J. Y., Cifuentes‐Rojas, C., Colognori, D., Jeon, Y., Szántó, A., Rosario, B. C. D., Pinter, S. F., et al. (2015) · Molecular Cell · doi:10.1016/j.molcel.2014.12.006 · Cited by 180
Cajal bodies are linked to genome conformation
Wang, Q., Sawyer, I. A., Sung, M.-H., Sturgill, D., Shevtsov, S. P., Pegoraro, G., Hakim, O., Baek, S., Hager, G. L., & Dundr, M. (2016) · Nature Communications · doi:10.1038/ncomms10966 · Cited by 164
Genomic Perspectives of Transcriptional Regulation in Forebrain Development
Nord, A. S., Pattabiraman, K., Visel, A., & Rubenstein, J. L. R. (2015) · Neuron · doi:10.1016/j.neuron.2014.11.011 · Cited by 152
Constructing 3D interaction maps from 1D epigenomes
Zhu, Y., Chen, Z., Zhang, K., Wang, M., Medovoy, D., Whitaker, J. W., Ding, B., Li, N., Zheng, L., & Wang, W. (2016) · Nature Communications · doi:10.1038/ncomms10812 · Cited by 146
Richard, D. J., Liu, Z., Cao, J., Kiapour, A. M., Willen, J., Yarlagadda, S., Jagoda, E., Kolachalama, V. B., Sieker, J. T., Chang, G. H., et al. (2020) · Cell · doi:10.1016/j.cell.2020.02.057 · Cited by 144
Diehl, A. G., Ouyang, N., & Boyle, A. P. (2020) · Nature Communications · doi:10.1038/s41467-020-15520-5 · Cited by 139
Long-read ChIA-PET for base-pair-resolution mapping of haplotype-specific chromatin interactions
Li, X., Luo, O. J., Wang, P., Zheng, M., Wang, D., Piecuch, E., Zhu, J. J., Tian, S. Z., Tang, Z., Li, G., et al. (2017) · Nature Protocols · doi:10.1038/nprot.2017.012 · Cited by 129
Chromatin Interaction Analysis with Paired-End Tag (ChIA-PET) sequencing technology and application
Li, G., Cai, L., Chang, H., Hong, P., Zhou, Q., Kulakova, E. V., Kolchanov, N. A., & Ruan, Y. (2014) · BMC Genomics · doi:10.1186/1471-2164-15-s12-s11 · Cited by 131
In the loop: promoter–enhancer interactions and bioinformatics
Mora, A., Sandve, G. K., Gabrielsen, O. S., & Eskeland, R. (2015) · Briefings in Bioinformatics · doi:10.1093/bib/bbv097 · Cited by 126
Emerging themes in cohesin cancer biology
Waldman, T. A. (2020) · Nature reviews. Cancer · doi:10.1038/s41568-020-0270-1 · Cited by 117
Enhancers with tissue-specific activity are enriched in intronic regionsPreprint
Borsari, B., Villegas-Mirón, P., Pérez-Lluch, S., Turpín, I., Laayouni, H., Segarra‐Casas, A., Bertranpetit, J., Guigó, R., & Acosta, S. (2021) · Genome Research · doi:10.1101/gr.270371.120 · Cited by 86
Kim, K.-D., Tanizawa, H., Iwasaki, O., & Noma, K.-I. (2016) · Nature Genetics · doi:10.1038/ng.3647 · Cited by 86
Contribution of Topological Domains and Loop Formation to 3D Chromatin Organization
Ea, V., Baudement, M.-O., Lesne, A., & Forné, T. (2015) · Genes · doi:10.3390/genes6030734 · Cited by 87
LDB1-mediated enhancer looping can be established independent of mediator and cohesin
Krivega, I. V., & Dean, A. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkx433 · Cited by 75
Gene regulation and chromatin organization: relevance of cohesin mutations to human disease
Watrin, E., Kaiser, F. J., & Wendt, K. S. (2016) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2015.12.004 · Cited by 69
Nipbl and Mediator Cooperatively Regulate Gene Expression to Control Limb Development
Muto, A., Ikeda, S., Lopez‐Burks, M. E., Kikuchi, Y., Calof, A. L., Lander, A. D., & Schilling, T. F. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004671 · Cited by 72
New themes in the biological functions of 5‐methylcytosine and 5‐hydroxymethylcytosine
Moen, E. L., Mariani, C. J., Zullow, H. J., Jeff‐Eke, M., Litwin, E., Nikitas, J. N., & Godley, L. A. (2014) · Immunological Reviews · doi:10.1111/imr.12242 · Cited by 66
Babu, D., & Fullwood, M. J. (2015) · Nucleus · doi:10.1080/19491034.2015.1106676 · Cited by 59
Next-Generation Sequencing and Epigenomics Research: A Hammer in Search of Nails
Sarda, S., & Hannenhalli, S. S. (2014) · Genomics & Informatics · doi:10.5808/gi.2014.12.1.2 · Cited by 58
Mechanisms of cohesin-mediated gene regulation and lessons learned from cohesinopathies
Ball, A. R., Chen, Y.-Y., & Yokomori, K. (2013) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2013.11.002 · Cited by 58
Bohla, D., Herold, M. V. B., Panzer, I., Buxa, M. K., Ali, T., Demmers, J., Krüger, M., Scharfe, M., Jarek, M., Bartkuhn, M., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0107765 · Cited by 58
Spatiotemporal regulation of GLI target genes in the mammalian limb bud
Lewandowski, J. P., Du, F., Zhang, S., Powell, M. B., Falkenstein, K. N., Ji, H., & Vokes, S. A. (2015) · Developmental Biology · doi:10.1016/j.ydbio.2015.07.022 · Cited by 54
Zhang, Z., Chng, K. R., Lingadahalli, S., Chen, Z., Liu, M. H., Do, H. H., Cai, S., Rinaldi, N. J., Poh, H. M., Li, G., et al. (2019) · Genome Research · doi:10.1101/gr.230243.117 · Cited by 54
Smith, O. K., & Aladjem, M. I. (2014) · Journal of Molecular Biology · doi:10.1016/j.jmb.2014.05.027 · Cited by 51
Towards genome-wide prediction and characterization of enhancers in plants
Marand, A. P., Zhang, T., Zhu, B., & Jiang, J. (2016) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2016.06.006 · Cited by 53
The Role of CCCTC-Binding Factor (CTCF) in Genomic Imprinting, Development, and Reproduction1
Franco, M. M., Prickett, A. R., & Oakey, R. J. (2014) · Biology of Reproduction · doi:10.1095/biolreprod.114.122945 · Cited by 53
TT‐seq captures enhancer landscapes immediately after T‐cell stimulation
Michel, M., Demel, C., Zacher, B., Schwalb, B., Krebs, S., Blum, H., Gagneur, J., & Cramer, P. (2017) · Molecular Systems Biology · doi:10.15252/msb.20167507 · Cited by 51
Grabbing the genome by the NADs
Matheson, T. D., & Kaufman, P. D. (2015) · Chromosoma · doi:10.1007/s00412-015-0527-8 · Cited by 46
Protein–DNA binding in high-resolution
Mahony, S., & Pugh, B. F. (2015) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.3109/10409238.2015.1051505 · Cited by 48
You, Q., Cheng, A. Y., Gu, X., Harada, B. T., Yu, M., Wu, T., Ren, B., Ouyang, Z., & He, C. (2020) · Nature Biotechnology · doi:10.1038/s41587-020-0643-8 · Cited by 46
Wong, B. K. Y., & Sutton, V. R. (2018) · American Journal of Medical Genetics Part C Seminars in Medical Genetics · doi:10.1002/ajmg.c.31658 · Cited by 44
Hi-TrAC reveals division of labor of transcription factors in organizing chromatin loops
Liu, S., Cao, Y., Cui, K., Tang, Q., & Zhao, K. (2022) · Nature Communications · doi:10.1038/s41467-022-34276-8 · Cited by 42
Improved transcription and translation with L-leucine stimulation of mTORC1 in Roberts syndrome
Xu, B., Gogol, M., Gaudenz, K., & Gerton, J. L. (2016) · BMC Genomics · doi:10.1186/s12864-015-2354-y · Cited by 40
Epigenomic and Transcriptomic Dynamics During Human Heart Organogenesis
VanOudenhove, J., Yankee, T. N., Wilderman, A. S., & Cotney, J. L. (2020) · Circulation Research · doi:10.1161/circresaha.120.316704 · Cited by 38
Self-citationEstrogen receptor-mediated long-range chromatin interactions and transcription in breast cancer
Liu, M. H., & Cheung, E. C. W. (2013) · Molecular and Cellular Endocrinology · doi:10.1016/j.mce.2013.09.019 · Cited by 40
The contribution of cohesin-SA1 to gene expression and chromatin architecture in two murine tissues
Cuadrado, A., Remeseiro, S., Graña‐Castro, O., Pisano, D. G., & Losada, A. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv144 · Cited by 38
Genome architecture: from linear organisation of chromatin to the 3D assembly in the nucleus
Sequeira‐Mendes, J., & Gutiérrez, C. (2015) · Chromosoma · doi:10.1007/s00412-015-0538-5 · Cited by 36
Kang, J. Y., Song, S., Yun, J., Jeon, M.-S., Kim, H. P., Han, S., & Kim, T. Y. (2015) · Oncogene · doi:10.1038/onc.2015.17 · Cited by 34
Haro, E., Petit, F., Pira, C. U., Spady, C., Lucas-Toca, S., Yorozuya, L. I., Gray, A. L., Escande, F., Jourdain, A., Nguyen, A., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-25844-5 · Cited by 34
Unraveling architecture of the pluripotent genome
Phillips‐Cremins, J. E. (2014) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2014.04.006 · Cited by 34
Limb-Enhancer Genie: An accessible resource of accurate enhancer predictions in the developing limb
Monti, R., Barozzi, I., Osterwalder, M., Lee, E., Kato, M., Garvin, T. H., Plajzer-Frick, I., Pickle, C. S., Akiyama, J. A., Afzal, V., et al. (2017) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1005720 · Cited by 32
Regulation and Dysregulation of Chromosome Structure in Cancer
Hnisz, D., Schuijers, J., Li, C. H., & Young, R. A. (2017) · Annual Review of Cancer Biology · doi:10.1146/annurev-cancerbio-030617-050134 · Cited by 31
Nagy, G., Czipa, E., Steiner, L., Nagy, T., Pongor, S., Nagy, L., & Barta, E. (2016) · BMC Genomics · doi:10.1186/s12864-016-2940-7 · Cited by 27
Lmx1b-targeted cis -regulatory modules involved in limb dorsalization
Haro, E., Watson, B. A., Feenstra, J. M., Tegeler, L., Pira, C. U., Mohan, S., & Oberg, K. C. (2017) · Development · doi:10.1242/dev.146332 · Cited by 28
The Yeast Genomes in Three Dimensions: Mechanisms and Functions
Noma, K.-I. (2017) · Annual Review of Genetics · doi:10.1146/annurev-genet-120116-023438 · Cited by 24
The nature of meiotic chromosome dynamics and recombination in budding yeast
Hong, S., Joo, J. H., Yun, H., & Kim, K. (2019) · The Journal of Microbiology · doi:10.1007/s12275-019-8541-9 · Cited by 25
Quintin, J., Péron, C. L., Palierne, G., Bizot, M., Cunha, S., Sérandour, A. A., Avner, S., Henry, C., Percevault, F., Belaud‐Rotureau, M., et al. (2014) · Molecular and Cellular Biology · doi:10.1128/mcb.00918-13 · Cited by 28
SMC complexes link gene expression and genome architecture
Dowen, J. M., & Young, R. A. (2014) · Current Opinion in Genetics & Development · doi:10.1016/j.gde.2013.11.009 · Cited by 25
Genome Editing in Neurosciences
Jaenisch, R., Gage, F. H., & Zhang, F. (2017) · Research and perspectives in neurosciences · doi:10.1007/978-3-319-60192-2 · Cited by 23
Li, X., Zeng, S., Chen, L., Zhang, Y., Li, X., Zhang, B., Su, D., Du, Q., Zhang, J., Wang, H., et al. (2023) · Cell Proliferation · doi:10.1111/cpr.13552 · Cited by 23
Zhang, H., Li, F., Jia, Y., Xu, B., Zhang, Y., Li, X., & Zhang, Z. (2017) · Nucleic Acids Research · doi:10.1093/nar/gkx885 · Cited by 18
Sarro, R., Kocher, A. A., Emera, D., Uebbing, S., Dutrow, E. V., Weatherbee, S. D., Nottoli, T., & Noonan, J. P. (2018) · Development · doi:10.1242/dev.158550 · Cited by 20
Self-citationLosa, M., Barozzi, I., Osterwalder, M., Hermosilla-Aguayo, V., Morabito, A., Chacón, B., Zarrineh, P., Girdziusaite, A., Benazet, J.-D., Zhu, J.-J., et al. (2022) · bioRxiv · doi:10.1038/s41467-023-39443-z · Cited by 15
Delta: a new web-based 3D genome visualization and analysis platform
Tang, B., Li, F., Li, J., Zhao, W., & Zhang, Z. (2017) · Bioinformatics · doi:10.1093/bioinformatics/btx805 · Cited by 16
Copy-number variants and candidate gene mutations in isolated split hand/foot malformation
Carter, T. C., Sicko, R. J., Kay, D. M., Browne, M. L., Romitti, P. A., Edmunds, Z. L., Liu, A., Fan, R., Druschel, C. M., Caggana, M., et al. (2017) · Journal of Human Genetics · doi:10.1038/jhg.2017.56 · Cited by 16
Tian, Y., Wang, G., Hu, Q., Xiao, X., & Chen, S. (2017) · Journal of Cellular Biochemistry · doi:10.1002/jcb.26587 · Cited by 16
Technologies to study spatial genome organization: beyond 3C
Übelmesser, N., & Papantonis, A. (2019) · Briefings in Functional Genomics · doi:10.1093/bfgp/elz019 · Cited by 13
Functional diversity of CTCFs is encoded in their binding motifs
Fang, R., Wang, C. C. Q., Skogerbø, G., & Zhang, Z. (2015) · BMC Genomics · doi:10.1186/s12864-015-1824-6 · Cited by 12
Bioinformatics approaches to predict target genes from transcription factor binding data
Essebier, A., Lamprecht, M. L., Piper, M., & Mikael Bodén, A. (2017) · Methods · doi:10.1016/j.ymeth.2017.09.001 · Cited by 13
Wood, A. M., Garza-Gongora, A. G., & Kosak, S. T. (2014) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2014.01.003 · Cited by 10
Borsari, B., Villegas-Mirón, P., Laayouni, H., Segarra‐Casas, A., Bertranpetit, J., Guigó, R., & Acosta, S. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.08.21.260836 · Cited by 9
Transcription-controlling regulatory elements of the eukaryotic genome
Razin, S. V., Gavrilov, A. A., & Ulianov, S. V. (2015) · Molecular Biology · doi:10.1134/s0026893315020119 · Cited by 8
Chromatin Organization and Transcriptional Programming of Breast Cancer Cell Identity
Bobbitt, J. R., Seachrist, D. D., & Keri, R. A. (2023) · Endocrinology · doi:10.1210/endocr/bqad100 · Cited by 9
IRX3/5 regulate mitotic chromatid segregation and limb bud shape
Tao, H., Lambert, J., Yung, T. M., Zhu, M. S., Hahn, N. A., Li, D., Lau, K. M., Sturgeon, K., Puviindran, V., Zhang, X., et al. (2020) · Development · doi:10.1242/dev.180042 · Cited by 8
Éot-Houllier, G., Magnaghi-Jaulin, L., Bourgine, G., Smagulova, F. O., Giet, R., Watrin, E., & Jaulin, C. (2023) · Journal of Cell Science · doi:10.1242/jcs.261014 · Cited by 5
Trim33 is required for appropriate development of pre-cardiogenic mesoderm
Rajderkar, S. S., Mann, J. M., Panaretos, C., Yumoto, K., Li, H., Mishina, Y. M., Ralston, B., & Kaartinen, V. (2019) · Developmental Biology · doi:10.1016/j.ydbio.2019.03.018 · Cited by 5
Britton, J. C., Somogyi-Leatigaga, A., Watson, B. A., Haro, E., Mulder, C. G., Kennedy, K., Cooper, A. M., Whitley, K., Yeboah, R., Kim, J., et al. (2025) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2025.1552716 · Cited by 4
Zou, J., Li, Z., Carleton, N. M., Oesterreich, S., Lee, A. V., & Tseng, G. C. (2024) · Bioinformatics · doi:10.1093/bioinformatics/btae696 · Cited by 4
In Vitro Modeling of Complex Neurological Diseases
Soldner, F., & Jaenisch, R. (2017) · Research and perspectives in neurosciences · doi:10.1007/978-3-319-60192-2_1 · Cited by 5
Genetically altered cancer epigenome
Tang, M., Luo, H., & Lu, J. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-799958-6.00012-3 · Cited by 4
Davidson, C., Wordsworth, B. P., Cohen, C., Knight, J. C., & Vecellio, M. L. (2023) · Frontiers in Genetics · doi:10.3389/fgene.2023.1129207 · Cited by 2
A Survey of the Computational Methods for Enhancers and Enhancer-target Predictions
Cao, Q., & Yip, K. Y.-L. (2016) · CRC Press eBooks · doi:10.1201/b20026-3 · Cited by 3
Zhang, Z., Wang, Z., & Zhang, J. (2025) · Physical review. E · doi:10.1103/r8rd-fykm · Cited by 2
Chromatin architecture and topology in pluripotent stem cells
Platania, A., & Sexton, T. (2020) · Elsevier eBooks · doi:10.1016/b978-0-12-814085-7.00004-0 · Cited by 3
Contribution of 3D Chromatin Architecture to the Maintenance of Pluripotency
Brant, L., & Papantonis, A. (2015) · Current Stem Cell Reports · doi:10.1007/s40778-015-0016-2 · Cited by 2
Chromatin Topology and Long- Range Genomic Interactions
Bayarsaihan, D. (2013) · Journal of Regenerative Medicine · doi:10.4172/2325-9620.1000e106 · Cited by 2
Treloar, A. E. (2016) · TSpace (University of Toronto) · Cited by 1
Hou, H. (2019) · TSpace (University of Toronto) · Cited by 1
Losa, M., Barozzi, I., Osterwalder, M., Zarrineh, P., Benazet, J. D., Chacón, B., Girdžiušaitė, A., Morabito, A., Zhu, J., Mackem, S., et al. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.03.08.483529 · Cited by 1
Losa, M., Barozzi, I., Osterwalder, M., Zarrineh, P., Benazet, J. D., Chacón, B., Girdžiušaitė, A., Morabito, A., Zhu, J., Mackem, S., et al. (2022) · Research Square · doi:10.21203/rs.3.rs-1460337/v1 · Cited by 1
Hi-TrAC reveals fine-scale chromatin structures organized by transcription factorsPreprint
Liu, S., Cao, Y., Cui, K., Tang, Q., & Zhao, K. (2022) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2022.06.01.494329 · Cited by 1
3D Genome Architecture in the Mammalian Nucleus
Enkhmandakh, B., & Bayarsaihan, D. (2013) · Epigenomics · doi:10.2217/epi.13.64
Metadata
- Authors
- DeMare, L. E., Leng, J., Cotney, J., Reilly, S. K., Yin, J., Sarro, R., & Noonan, J. P.
- Affiliations
- Yale University (US)
- Corresponding author
- Noonan, James P.
- Venue
- Genome Research
- Publisher
- Cold Spring Harbor Laboratory
- Published
- 2013-05-23
- Volume
- 23
- Issue
- 8
- Pages
- 1224-1234
- ISSN
- 1088-9051 (ISSN-L)
- PMC
- PMC3730097
- OpenAlex
- W2024640399
- Cited by
- 114
- References
- 63
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 2 · 2023: 5 · 2022: 4 · 2021: 2 · 2020: 10 · 2019: 6 · 2018: 3 · 2017: 20 · 2016: 12 · 2015: 19 · 2014: 18 · 2013: 9
- Type
- posted content
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Genome Research (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion, cc-by-nc)
- PubMed Central (publishedVersion, cc-by-nc)
- PubMed (publishedVersion)
- HighWire Press Open Archive (submittedVersion)
- Funders
- National Science Foundation
- Howard Hughes Medical Institute
- Edward Mallinckrodt, Jr. Foundation
- National Institutes of Health
- National Institute of General Medical Sciences (T32GM007223, GM094780, R01GM094780)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (T32HD007149)
- 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 › Epigenetics and DNA Methylation
- Keywords
- cohesin, SMC1A, CTCF, chromatin interactions, enhancer-promoter interactions, insulator proteins, tissue-specific gene regulation, limb development, embryonic stem cells, chromatin looping, regulatory architecture, mouse embryo
- MeSH terms
- CCCTC-Binding Factor, Cohesins, Structural Maintenance of Chromosome Protein 1, Animals, Binding Sites, Chromatin, Chromosomal Proteins, Non-Histone, Enhancer Elements, Genetic, Histones, Mice, Inbred C57BL, Organ Specificity, Promoter Regions, Genetic, Repressor Proteins, Genome, Gene Expression Regulation, Developmental, Cell Cycle Proteins, Limb Buds, Protein Subunits, Chromatin Immunoprecipitation, Mice
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