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      Multi-contact 3C reveals that the human genome during interphase is largely not entangled

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          Abstract

          During interphase the eukaryotic genome is organized into chromosome territories that are spatially segregated into compartment domains. The extent to which interacting domains or chromosomes are entangled is not known. We analyze series of co-occurring chromatin interactions using multi-contact 3C (MC-3C) in human cells to provide insights into the topological entanglement of chromatin. Multi-contact interactions represent percolation paths (C-walks) through 3D chromatin space. We find that the order of interactions within C-walks that occur across interfaces where chromosomes or compartment domains interact is not random. Polymer simulations show that such C-walks are consistent with distal domains being topologically insulated, i.e. not catenated. Simulations show that even low levels of random strand passage, e.g. by topoisomerase II, would result in entanglements, increased mixing at domain interfaces and an order of interactions within C-walks not consistent with experimental MC-3C data. Our results indicate that during interphase entanglements between chromosomes and chromosomal domains are rare.

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          Most cited references56

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          A 3D map of the human genome at kilobase resolution reveals principles of chromatin looping.

          We use in situ Hi-C to probe the 3D architecture of genomes, constructing haploid and diploid maps of nine cell types. The densest, in human lymphoblastoid cells, contains 4.9 billion contacts, achieving 1 kb resolution. We find that genomes are partitioned into contact domains (median length, 185 kb), which are associated with distinct patterns of histone marks and segregate into six subcompartments. We identify ∼10,000 loops. These loops frequently link promoters and enhancers, correlate with gene activation, and show conservation across cell types and species. Loop anchors typically occur at domain boundaries and bind CTCF. CTCF sites at loop anchors occur predominantly (>90%) in a convergent orientation, with the asymmetric motifs "facing" one another. The inactive X chromosome splits into two massive domains and contains large loops anchored at CTCF-binding repeats. Copyright © 2014 Elsevier Inc. All rights reserved.
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            Comprehensive mapping of long-range interactions reveals folding principles of the human genome.

            We describe Hi-C, a method that probes the three-dimensional architecture of whole genomes by coupling proximity-based ligation with massively parallel sequencing. We constructed spatial proximity maps of the human genome with Hi-C at a resolution of 1 megabase. These maps confirm the presence of chromosome territories and the spatial proximity of small, gene-rich chromosomes. We identified an additional level of genome organization that is characterized by the spatial segregation of open and closed chromatin to form two genome-wide compartments. At the megabase scale, the chromatin conformation is consistent with a fractal globule, a knot-free, polymer conformation that enables maximally dense packing while preserving the ability to easily fold and unfold any genomic locus. The fractal globule is distinct from the more commonly used globular equilibrium model. Our results demonstrate the power of Hi-C to map the dynamic conformations of whole genomes.
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              Aligning sequence reads, clone sequences and assembly Contigs with BWA-MEM

              L H, H Li, H. Li (2013)
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                Author and article information

                Journal
                101186374
                31761
                Nat Struct Mol Biol
                Nat Struct Mol Biol
                Nature structural & molecular biology
                1545-9993
                1545-9985
                18 August 2020
                14 September 2020
                December 2020
                14 March 2021
                : 27
                : 12
                : 1105-1114
                Affiliations
                [1 ]Program in Systems Biology, Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, MA, 01605, USA
                [2 ]Howard Hughes Medical Institute, Chevy Chase, MD 20815, USA
                Author notes
                [# ]Correspondence: Job Dekker ( Job.Dekker@ 123456umassmed.edu )
                [$ ]Correspondence for modeling and simulation parts: Davood Norouzi ( Davood.Norouzi@ 123456umassmed.edu )

                AUTHOR CONTRIBUTIONS

                J.D. designed the project. B.D. and Y.L. performed the experimental MC-3C procedure. F.T-C. and D.N. analyzed the data. D.N. designed and performed the simulations. F.T-C., D.N., and J.D. wrote the paper.

                [*]

                These authors contributed equally

                Article
                NIHMS1620196
                10.1038/s41594-020-0506-5
                7718335
                32929283
                b48f1342-f76f-48d5-b542-c4e55e42d186

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                Molecular biology
                Molecular biology

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