Cited by 279CRISPR and Genetic EngineeringGenomics and Chromatin DynamicsChromatin Remodeling and Cancer

Manipulation of nuclear architecture through CRISPR-mediated chromosomal looping

Open access
Morgan, Stefanie L., Mariano, Natasha C., Bermudez, Abel, Arruda, Nicole L., Wu, Fangting, Luo, Yunhai, Shankar, Gautam, Jia, Lin +6 more·2017·Nature Communications

Abstract

Chromatin looping is key to gene regulation, yet no broadly applicable methods to selectively modify chromatin loops have been described. We have engineered a method for chromatin loop reorganization using CRISPR-dCas9 (CLOuD9) to selectively and reversibly establish chromatin loops. We demonstrate the power of this technology to selectively modulate gene expression at targeted loci.

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Crossref · 10.1038/ncomms15993

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  • Stimulation of promoter activity by forced looping with an enhancer is a strong argument in favor of the loop model.

    “Stimulation of promoter activity by forced looping with an enhancer is a strong argument in favor of this model [87,88,110,111].”

    From Enhancer Function in the 3D Genome (2023) · cites this paper as [110]

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Cites

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Research works printed but not linked: 15

  1. Krivega I. & Dean A. Chromatin looping as a target for altering erythroid gene expression. Ann. N.Y. Acad. Sci. 1368, 31– 39 (2016). 26918894 PMC4870130
  2. Matharu N. & Ahituv N. Minor loops in major folds: Enhancer-promoter looping, chromatin restructuring, and their association with transcriptional regulation and disease. PLoS Genet. 11, e1005640 (2015). 26632825 PMC4669122
  3. Kim A. & Dean A. Chromatin loop formation in the β-globin locus and its role in globin gene transcription. Mol Cells. 34, 1– 5 (2012). 22610406 PMC3887778
  4. Stadhouders R.. Transcription regulation by distal enhancers. Transcription 3, 181– 186 (2012). 22771987 PMC3654767
  5. van Steensel B. & Dekker J. Genomics tools for unraveling chromosome architecture. Nat. Biotechnol. 28, 1089– 1095 (2010). 20944601 PMC3023824
  6. Petrascheck M.. DNA looping induced by a transcriptional enhancer in vivo. Nucleic Acids Res. 33, 3743– 3750 (2005). 16002789 PMC1174898
  7. Ameres S. L.. Inducible DNA-loop formation blocks transcriptional activation by an SV40 enhancer. EMBO J. 24, 358– 367 (2005). 15650749 PMC545818
  8. Liang F.-S., Ho W. Q. & Crabtree G. R. Engineering the ABA plant stress pathway for regulation of induced proximity. Sci. Signal. 4, rs2 (2011). 21406691 PMC3110149
  9. Theunissen T. W.. Systematic identification of culture conditions for induction and maintenance of naive human pluripotency. Cell Stem Cell. 15, 471– 487 (2014). 25090446 PMC4184977
  10. Zhang H.. Intrachromosomal looping is required for activation of endogenous pluripotency genes during reprogramming. Cell Stem Cell. 13, 30– 35 (2013). 23747202
  11. Mokry M.. Integrated genome-wide analysis of transcription factor occupancy, RNA polymerase II binding and steady state RNA levels identify differentially regulated functional gene classes. Nucleic Acids Res. 40, 148– 158 (2012). 21914722 PMC3245935
  12. Drier Y.. An oncogenic MYB feedback loop drives alternate cell fates in adenoid cystic carcinoma. Nat Genet. 48, 265– 272 (2016). 26829750 PMC4767593
  13. Ryan R. J. H.. Detection of enhancer-associated rearrangements reveals mechanisms of oncogene dysregulation in B-cell lymphoma. Cancer Discov 5, 1058– 1071 (2015). 26229090 PMC4592453
  14. Montavon T.. A regulatory archipelago controls Hox genes transcription in digits. Cell 147, 1132– 1145 (2011). 22118467
  15. Lupianez D. G.. Disruptions of topological chromatin domains cause pathogenic rewiring of gene-enhancer interactions. Cell 161, 1012– 1025 (2015). 25959774 PMC4791538

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Authors
Morgan, S. L., Mariano, N. C., Bermudez, A., Arruda, N. L., Wu, F., Luo, Y., Shankar, G., Jia, L., Chen, H., Hu, J.-F., Hoffman, A. R., Huang, C.-C., Pitteri, S. J., & Wang, K. C.
Affiliations
  • Stanford Medicine (US)
  • Bridgewater State University (US)
  • System Biosciences (United States) (US)
  • Jilin University (CN)
  • Central South University (CN)
  • VA Palo Alto Health Care System (US)
Venue
Nature Communications
Published
2017-07-13
Volume
8
Issue
1
Pages
15993-15993
ISSN
2041-1723 (ISSN-L)
OpenAlex
W2736242246
Cited by
279
References
3
Citations by year
2026: 13 · 2025: 22 · 2024: 19 · 2023: 26 · 2022: 33 · 2021: 46 · 2020: 39 · 2019: 41 · 2018: 34 · 2017: 6
FWCI
13.41
Type
journal article
Language
en
Open access
Locations
  • Nature Communications (publishedVersion, cc-by)
  • Europe PMC (PubMed Central) (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • RePEc: Research Papers in Economics (submittedVersion)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
  • National Science Foundation
  • U.S. Department of Veterans Affairs (I01 BX002905)
  • Burroughs Wellcome Fund
  • Donald E. and Delia B. Baxter Foundation
  • National Defense Science and Engineering Graduate
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › CRISPR and Genetic Engineering
  • 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
Keywords
chromatin looping, CRISPR/dCas9, nuclear organization, gene expression regulation, gene expression modulation
MeSH terms
Humans, Promoter Regions, Genetic, K562 Cells, Chromatin Assembly and Disassembly, DEAD-box RNA Helicases, beta-Globins, HEK293 Cells, CRISPR-Cas Systems

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