The DOI matches its Crossref record; 48 of the 48 references it cites were found in a registry or an index.
Looping and Interaction between Hypersensitive Sites in the Active β-globin Locus
Open accessAbstract
Eukaryotic transcription can be regulated over tens or even hundreds of kilobases. We show that such long-range gene regulation in vivo involves spatial interactions between transcriptional elements, with intervening chromatin looping out. The spatial organization of a 200 kb region spanning the murine beta-globin locus was analyzed in expressing erythroid and nonexpressing brain tissue. In brain, the globin cluster adopts a seemingly linear conformation. In erythroid cells the hypersensitive sites of the locus control region (LCR), located 40-60 kb away from the active genes, come in close spatial proximity with these genes. The intervening chromatin with inactive globin genes loops out. Moreover, two distant hypersensitive regions participate in these interactions. We propose that clustering of regulatory elements is key to creating and maintaining active chromatin domains and regulating transcription.
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In the citing paper
“3C confirmed that the LCR comes into close contact with active β-globin genes, whilst the intervening inactive genes are looped out [266].”
From Transcriptional enhancers and their communication with gene promoters (2021) · cites this paper as [266]
In the citing paper
“Two papers published in 2002 used different novel biochemical techniques to demonstrate that the β-globin LCR forms chromosomal loops with the active β-globin genes in vivo.”
From Transcriptional enhancers and their communication with gene promoters (2021) · cites this paper as [266]
In the citing paper
“Enhancer–promoter looping occurred in erythroid cells, in which the β-globin genes are expressed, but not in brain cells, in which they are not [266].”
From Transcriptional enhancers and their communication with gene promoters (2021) · cites this paper as [266]
In the citing paper
“It has been shown that remote enhancers in the mouse β-globin gene domain form a single complex to which the genes that need to be activated are recruited [32].”
From Enhancer Function in the 3D Genome (2023) · cites this paper as [32]
In the citing paper
“First, it was shown that active enhancers are often in physical proximity to the promoters they activate, regardless of the genomic distances between these enhancers and promoters [32,33,34].”
From Enhancer Function in the 3D Genome (2023) · cites this paper as [32]
In the citing paper
“In erythroid cells expressing globin genes, a large CTCF-CTCF loop encompasses the beta-globin genes and the locus control region (LCR), consistent with the organization of the locus in an insulated neighborhood.”
From Insulated Neighborhoods: Structural and Functional Units of Mammalian Gene Control (2016) · cites this paper as Tolhuis et al., 2002
In the citing paper
“In fetal brain cells, CTCF binding to one of the beta-globin loop anchor regions is absent and CTCF-CTCF loop formation is not detected (Splinter et al., 2006; Tolhuis et al., 2002), which suggests that tissue-specific CTCF-CTCF loops participate in developmental gene control.”
From Insulated Neighborhoods: Structural and Functional Units of Mammalian Gene Control (2016) · cites this paper as Tolhuis et al., 2002
In the citing paper
“Central to the mechanism of globin gene switching is the exclusive interaction between the LCR and globin gene promoters at distinct developmental stages (Carter et al., 2002; Palstra et al., 2008; Tolhuis et al., 2002).”
From Reactivation of developmentally silenced globin genes by forced chromatin looping (2014) · cites this paper as Tolhuis et al., 2002
In the citing paper
“In erythroid cells, a powerful distal enhancer called the locus control region (LCR), composed of multiple DNase I hypersensitive sites (HSs), is in physical proximity to the β-globin genes in a developmentally dynamic manner (Carter et al., 2002; Tolhuis et al., 2002).”
From Reactivation of developmentally silenced globin genes by forced chromatin looping (2014) · cites this paper as Tolhuis et al., 2002
Citations
Cites
Capturing Chromosome Conformation
Dekker, J., Rippe, K., Dekker, M., & Kleckner, N. (2002) · Science · doi:10.1126/science.1067799 · Cited by 3,652
Position-independent, high-level expression of the human β-globin gene in transgenic mice
Grosveld, F. G., van Assendelft, G. B., Greaves, D. R., & Kollias, G. A. (1987) · Cell · doi:10.1016/0092-8674(87)90584-8 · Cited by 1,908
Self-citationExpression of a β-globin gene is enhanced by remote SV40 DNA sequences
Banerji, J., Rusconi, S., & Schaffner, W. (1981) · Cell · doi:10.1016/0092-8674(81)90413-x · Cited by 1,724
Gene regulation by proteins acting nearby and at a distance
Ptashne, M. (1986) · Nature · doi:10.1038/322697a0 · Cited by 860
Insulators: many functions, many mechanismsPreprint
West, A. G., Gaszner, M., & Felsenfeld, G. (2002) · Genes & Development · doi:10.1101/gad.954702 · Cited by 624
A position-effect assay for boundaries of higher order chromosomal domains
Kellum, R., & Schedl, P. D. (1991) · Cell · doi:10.1016/0092-8674(91)90318-s · Cited by 616
The "beta-like-globin" gene domain in human erythroid cells.
Tuan, D., Solomon, W., Li, Q., & London, I. M. (1985) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.82.19.6384 · Cited by 601
Transcription complex stability and chromatin dynamics in vivo
Wijgerde, M., Grosveld, F. G., & Fraser, P. (1995) · Nature · doi:10.1038/377209a0 · Cited by 471
Self-citationHeterochromatin Effects on the Frequency and Duration of LCR-Mediated Gene Transcription
Milot, E., Strouboulis, J., Trimborn, T., Wijgerde, M., de Boer, E., Langeveld, A., Tan-Un, K., Vergeer, W., Yannoutsos, N., Grosveld, F., et al. (1996) · Cell · doi:10.1016/s0092-8674(00)81327-6 · Cited by 314
Self-citationLOCKE, J. L., Kotarski, M. A., & Tartof, K. D. (1988) · Genetics · doi:10.1093/genetics/120.1.181 · Cited by 313
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Pliner, H. A., Packer, J., McFaline-Figueroa, J. L., Cusanovich, D. A., Daza, R., Srivatsan, S., Qiu, X., Jackson, D., Minkina, A., Adey, A., et al. (2017) · doi:10.1101/155473 · Cited by 16
Between form and function: the complexity of genome folding
Oudelaar, A. M., Hanssen, L. L. P., Hardison, R. C., Kassouf, M. T., Hughes, J. R., & Higgs, D. R. (2017) · Human Molecular Genetics · doi:10.1093/hmg/ddx306 · Cited by 16
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He, C., Wang, X., & Zhang, M. Q. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku327 · Cited by 16
3D genomics imposes evolution of the domain model of eukaryotic genome organization
Razin, S. V., & Vassetzky, Y. S. (2016) · Chromosoma · doi:10.1007/s00412-016-0604-7 · Cited by 16
Knoch, T. (2018) · Seminars in Cell and Developmental Biology · doi:10.1016/j.semcdb.2018.07.012 · Cited by 16
Rodríguez, S., Scadden, A. W., Reckard, A. T., Shtanko, Y., Hull-Crew, C., & Klocko, A. D. (2022) · G3 Genes Genomes Genetics · doi:10.1093/g3journal/jkac053 · Cited by 18
Melnikova, L. S., Kostuchenko, M., Silicheva, M., & Georgiev, P. G. (2007) · Chromosoma · doi:10.1007/s00412-007-0132-6 · Cited by 16
Bredenbeck, A., Hollstein, V. M., Trefzer, U., Sterry, W., Walden, P., & Losch, F. (2008) · Gene · doi:10.1016/j.gene.2008.02.019 · Cited by 16
Gross, D. S., Chowdhary, S., Anandhakumar, J., & Kainth, A. S. (2015) · Current Biology · doi:10.1016/j.cub.2015.10.059 · Cited by 16
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Zhang, Y., See, Y. X., Tergaonkar, V., & Fullwood, M. J. (2022) · Cells · doi:10.3390/cells11091560 · Cited by 17
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Sawado, T., Halow, J. M., Im, H., Ragoczy, T., Bresnick, E. H., Bender, M. A., & Groudine, M. T. (2008) · Blood · doi:10.1182/blood-2007-12-128983 · Cited by 15
Ross, J., Bottardi, S., Bourgoin, V., Wollenschlaeger, A., Drobetsky, E. A., Trudel, M., & Milot, É. (2009) · Nucleic Acids Research · doi:10.1093/nar/gkp545 · Cited by 15
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Rezzoug, F., Thomas, S. D., Rouchka, E. C., & Miller, D. M. (2016) · PLoS ONE · doi:10.1371/journal.pone.0161588 · Cited by 13
Weber, B., Jamge, S., & Stam, M. E. (2017) · Methods in molecular biology · doi:10.1007/978-1-4939-7318-7_15 · Cited by 13
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Barrow, J. J., Li, Y., Hossain, M. A., Huang, S., & Bungert, J. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku107 · Cited by 13
Kolovos, P., Brouwer, R. W. W., Kockx, C. E. M., Lesnussa, M., Kepper, N., Zuin, J., Imam, A., van de Werken, H. J. G., Wendt, K. S., Knoch, T., et al. (2018) · Nature Protocols · doi:10.1038/nprot.2017.132 · Cited by 14
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Du, M., Lv, X., Hao, D., Zhao, G., Wu, X., Wu, F., Liu, D., & Liang, C. (2007) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2007.11.004 · Cited by 13
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Liu, L., Karmakar, S., Dhar, R., Mahajan, M. C., Choudhury, A., Weissman, S. M., & Pace, B. S. (2013) · PLoS ONE · doi:10.1371/journal.pone.0078253 · Cited by 13
Hamid, M., Mahjoubi, F., Akbari, M. T., Arab, A., Zeinali, S., & Karimipoor, M. (2009) · Hemoglobin · doi:10.3109/03630260903336479 · Cited by 13
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Bieker, J. J., & Philipsen, S. (2024) · Advances in experimental medicine and biology · doi:10.1007/978-3-031-62731-6_10 · Cited by 15
Lineage-specific combinatorial action of enhancers regulates mouse erythroid Gata1 expression.
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Smits, W. K., Vermeulen, C., Hagelaar, R., Kimura, S., Vroegindeweij, E. M., Buijs-Gladdines, J. G. C. A. M., van de Geer, E., Verstegen, M. J. A. M., Splinter, E., van Reijmersdal, S. V., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112373 · Cited by 13
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Tokuda, N., Sasai, M., & Chikenji, G. (2011) · Biophysical Journal · doi:10.1016/j.bpj.2010.11.016 · Cited by 12
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Hoang, S. A., & Bekiranov, S. (2013) · PLoS ONE · doi:10.1371/journal.pone.0081972 · Cited by 12
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McCord, R. P., Zhou, V. W., Yuh, T., & Bulyk, M. L. (2011) · Genomics · doi:10.1016/j.ygeno.2011.08.003 · Cited by 12
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Davidson, S., Macpherson, N. N., & Mitchell, J. A. (2013) · Biochemistry and Cell Biology · doi:10.1139/bcb-2012-0059 · Cited by 12
Wang, J., Meng, X., Chen, H., Yuan, C., Li, X., Zhou, Y., & Chen, M. (2016) · Briefings in Functional Genomics · doi:10.1093/bfgp/elv062 · Cited by 12
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Fan, J., Xu, Y., Wen, X., Ge, S., Jia, R., Zhang, H., & Fan, X. (2019) · Molecular Therapy · doi:10.1016/j.ymthe.2019.07.020 · Cited by 12
Otto, C. N. (2020) · Elsevier eBooks · doi:10.1016/b978-0-323-53045-3.00016-7 · Cited by 12
Osborne, C. S., & Eskiw, C. H. (2008) · Journal of Cellular Biochemistry · doi:10.1002/jcb.21750 · Cited by 12
Chan, P. K., Wai, A., Philipsen, S., & Tan-Un, K. (2008) · PLoS ONE · doi:10.1371/journal.pone.0002134 · Cited by 12
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Lee, J., Min, H., Wang, X., Khan, A. A., & Kim, M. H. (2010) · Anatomy & Cell Biology · doi:10.5115/acb.2010.43.1.78 · Cited by 12
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Waldispühl, J., Zhang, E., Butyaev, A., Nazarova, E., & Cyr, Y. (2018) · Methods · doi:10.1016/j.ymeth.2018.05.008 · Cited by 13
Patrinos, G. P., & Antonarakis, S. E. (2009) · Springer eBooks · doi:10.1007/978-3-540-37654-5_13 · Cited by 12
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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
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Self-citationLiu, M., Huang, K., Zhang, J., Li, Q., Wang, X., Gu, B.-M., Tang, H., Du, Z., Hu, L., Qi, S., et al. (2025) · Nature Biotechnology · doi:10.1038/s41587-025-02887-3 · Cited by 13
Schmitt, M. J., Dramaretska, Y., Serresi, M., Kertalli, S., Jiang, B., Yin, J., Aguzzi, A., Barozzi, I., & Gargiulo, G. (2024) · Nature Communications · doi:10.1038/s41467-024-45069-6 · Cited by 13
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Meyer, C. A., Tang, Q., & Liu, X. S. (2012) · Molecular Endocrinology · doi:10.1210/me.2012-1150 · Cited by 11
Saiz, L., & Vilar, J. M. G. (2008) · IET Systems Biology · doi:10.1049/iet-syb:20080091 · Cited by 11
Zhu, X., Xi, C., Ward, A., Takezaki, M., Shi, H., Peterson, K. R., & Pace, B. S. (2020) · Experimental Biology and Medicine · doi:10.1177/1535370220945305 · Cited by 11
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Metadata
- Authors
- Tolhuis, B., Palstra, R.-J., Splinter, E., Grosveld, F., & de Laat, W.
- Affiliations
- Erasmus University Rotterdam (NL)
- Venue
- Molecular Cell
- Publisher
- Elsevier BV
- Published
- 2002-12
- Volume
- 10
- Issue
- 6
- Pages
- 1453-1465
- ISSN
- 1097-2765 (ISSN-L)
- OpenAlex
- W2089894746
- Cited by
- 1,344
- References
- 48
- Citations by year
- 2026: 19 · 2025: 23 · 2024: 39 · 2023: 26 · 2022: 38 · 2021: 44 · 2020: 46 · 2019: 55 · 2018: 58 · 2017: 58 · 2016: 70 · 2015: 68 · 2014: 76 · 2013: 62 · 2012: 84
- FWCI
- 15.10
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Molecular Cell (publishedVersion)
- PubMed (publishedVersion)
- EUR Research Repository (Erasmus University Rotterdam) (submittedVersion)
- 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
- Health Sciences › Medicine › Genetics (clinical) › Hemoglobinopathies and Related Disorders
- Keywords
- chromatin looping, long-range gene regulation, beta-globin locus control region, hypersensitive sites, chromatin domains, erythroid cells, brain tissue, transcriptional regulation
- MeSH terms
- Animals, Binding Sites, Brain, Chromatin, Chromosome Mapping, DNA, Multigene Family, Globins, Liver, Nucleic Acid Conformation, Locus Control Region, Mice
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