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      Hierarchical folding and reorganization of chromosomes are linked to transcriptional changes in cellular differentiation

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          Abstract

          Mammalian chromosomes fold into arrays of megabase‐sized topologically associating domains ( TADs), which are arranged into compartments spanning multiple megabases of genomic DNA. TADs have internal substructures that are often cell type specific, but their higher‐order organization remains elusive. Here, we investigate TAD higher‐order interactions with Hi‐C through neuronal differentiation and show that they form a hierarchy of domains‐within‐domains (meta TADs) extending across genomic scales up to the range of entire chromosomes. We find that TAD interactions are well captured by tree‐like, hierarchical structures irrespective of cell type. meta TAD tree structures correlate with genetic, epigenomic and expression features, and structural tree rearrangements during differentiation are linked to transcriptional state changes. Using polymer modelling, we demonstrate that hierarchical folding promotes efficient chromatin packaging without the loss of contact specificity, highlighting a role far beyond the simple need for packing efficiency.

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          Most cited references18

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          Hierarchical organization of modularity in metabolic networks

          Spatially or chemically isolated functional modules composed of several cellular components and carrying discrete functions are considered fundamental building blocks of cellular organization, but their presence in highly integrated biochemical networks lacks quantitative support. Here we show that the metabolic networks of 43 distinct organisms are organized into many small, highly connected topologic modules that combine in a hierarchical manner into larger, less cohesive units, their number and degree of clustering following a power law. Within Escherichia coli the uncovered hierarchical modularity closely overlaps with known metabolic functions. The identified network architecture may be generic to system-level cellular organization.
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            Architectural protein subclasses shape 3D organization of genomes during lineage commitment.

            Understanding the topological configurations of chromatin may reveal valuable insights into how the genome and epigenome act in concert to control cell fate during development. Here, we generate high-resolution architecture maps across seven genomic loci in embryonic stem cells and neural progenitor cells. We observe a hierarchy of 3D interactions that undergo marked reorganization at the submegabase scale during differentiation. Distinct combinations of CCCTC-binding factor (CTCF), Mediator, and cohesin show widespread enrichment in chromatin interactions at different length scales. CTCF/cohesin anchor long-range constitutive interactions that might form the topological basis for invariant subdomains. Conversely, Mediator/cohesin bridge short-range enhancer-promoter interactions within and between larger subdomains. Knockdown of Smc1 or Med12 in embryonic stem cells results in disruption of spatial architecture and downregulation of genes found in cohesin-mediated interactions. We conclude that cell-type-specific chromatin organization occurs at the submegabase scale and that architectural proteins shape the genome in hierarchical length scales. Copyright © 2013 Elsevier Inc. All rights reserved.
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              Genome architecture: domain organization of interphase chromosomes.

              The architecture of interphase chromosomes is important for the regulation of gene expression and genome maintenance. Chromosomes are linearly segmented into hundreds of domains with different protein compositions. Furthermore, the spatial organization of chromosomes is nonrandom and is characterized by many local and long-range contacts among genes and other sequence elements. A variety of genome-wide mapping techniques have made it possible to chart these properties at high resolution. Combined with microscopy and computational modeling, the results begin to yield a more coherent picture that integrates linear and three-dimensional (3D) views of chromosome organization in relation to gene regulation and other nuclear functions. Copyright © 2013 Elsevier Inc. All rights reserved.
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                Author and article information

                Journal
                Mol Syst Biol
                Mol. Syst. Biol
                10.1002/(ISSN)1744-4292
                MSB
                msb
                Molecular Systems Biology
                John Wiley and Sons Inc. (Hoboken )
                1744-4292
                28 December 2015
                December 2015
                : 11
                : 12 ( doiID: 10.1002/msb.v11.12 )
                : 852
                Affiliations
                [ 1 ] Department of Biochemistry Goodman Cancer CentreMcGill University Montréal QCCanada
                [ 2 ] Epigenetic Regulation and Chromatin Architecture Group Berlin Institute for Medical Systems BiologyMax‐Delbrück Centre for Molecular Medicine Berlin‐BuchGermany
                [ 3 ] Genome Function Group MRC Clinical Sciences CentreImperial College London Hammersmith Hospital Campus LondonUK
                [ 4 ] Dipartimento di FisicaUniversità di Napoli Federico II INFN Napoli CNR‐SPIN Complesso Universitario di Monte Sant'Angelo NaplesItaly
                [ 5 ] MRC Human Genetics UnitMRC IGMM University of Edinburgh EdinburghUK
                [ 6 ]RIKEN Preventive Medicine and Diagnosis Innovation Program Wako SaitamaJapan
                [ 7 ] Division of Genomic TechnologiesRIKEN Center for Life Science Technologies Yokohama KanagawaJapan
                [ 8 ] Stem Cell Neurogenesis Group MRC Clinical Sciences CentreImperial College London Hammersmith Hospital Campus LondonUK
                [ 9 ] Single Molecule Imaging Group MRC Clinical Sciences CentreImperial College London Hammersmith Hospital Campus LondonUK
                [ 10 ]Cardiff School of Biosciences CardiffUK
                [ 11 ] Systems Biology and GenomicsHarry Perkins Institute of Medical Research Nedlands WAAustralia
                Author notes
                [*] [* ] Corresponding author. Tel: +44 131 651 8614; E‐mail: colin.semple@ 123456igmm.ed.ac.uk

                Corresponding author. Tel: +1 514 398 4975; E‐mail: josee.dostie@ 123456mcgill.ca

                Corresponding author. Tel: +49 30 94061752; E‐mail: ana.pombo@ 123456mdc-berlin.de

                Corresponding author. Tel: +39 081 676475; E‐mail: mario.nicodemi@ 123456na.infn.it

                [†]

                These authors contributed equally to this work

                Article
                MSB156492
                10.15252/msb.20156492
                4704492
                26700852
                145fed89-f3b0-4d6b-8e92-373ebfaa892c
                © 2015 The Authors. Published under the terms of the CC BY 4.0 license

                This is an open access article under the terms of the Creative Commons Attribution 4.0 License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 07 August 2015
                : 26 November 2015
                : 27 November 2015
                Page count
                Pages: 14
                Funding
                Funded by: Canadian Institutes of Health Research (CIHR)
                Award ID: MOP‐86716
                Award ID: CAP‐120350
                Funded by: Helmholtz Foundation (Germany)
                Funded by: MEXT
                Categories
                Embo09
                Embo11
                Embo17
                Article
                Articles
                Custom metadata
                2.0
                msb156492
                December 2015
                Converter:WILEY_ML3GV2_TO_NLMPMC version:4.7.2 mode:remove_FC converted:07.01.2016

                Quantitative & Systems biology
                chromatin contacts,chromosome architecture,epigenetics,gene expression,polymer modelling

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