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      Chromatin Insulator Factors Involved in Long-Range DNA Interactions and Their Role in the Folding of the Drosophila Genome

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          Abstract

          Chromatin insulators are genetic elements implicated in the organization of chromatin and the regulation of transcription. In Drosophila, different insulator types were characterized by their locus-specific composition of insulator proteins and co-factors. Insulators mediate specific long-range DNA contacts required for the three dimensional organization of the interphase nucleus and for transcription regulation, but the mechanisms underlying the formation of these contacts is currently unknown. Here, we investigate the molecular associations between different components of insulator complexes (BEAF32, CP190 and Chromator) by biochemical and biophysical means, and develop a novel single-molecule assay to determine what factors are necessary and essential for the formation of long-range DNA interactions. We show that BEAF32 is able to bind DNA specifically and with high affinity, but not to bridge long-range interactions (LRI). In contrast, we show that CP190 and Chromator are able to mediate LRI between specifically-bound BEAF32 nucleoprotein complexes in vitro. This ability of CP190 and Chromator to establish LRI requires specific contacts between BEAF32 and their C-terminal domains, and dimerization through their N-terminal domains. In particular, the BTB/POZ domains of CP190 form a strict homodimer, and its C-terminal domain interacts with several insulator binding proteins. We propose a general model for insulator function in which BEAF32/dCTCF/Su(HW) provide DNA specificity (first layer proteins) whereas CP190/Chromator are responsible for the physical interactions required for long-range contacts (second layer). This network of organized, multi-layer interactions could explain the different activities of insulators as chromatin barriers, enhancer blockers, and transcriptional regulators, and suggest a general mechanism for how insulators may shape the organization of higher-order chromatin during cell division.

          Author Summary

          Chromatin insulators mediate specific long-range DNA interactions required for the three dimensional organization of the interphase nucleus and for transcription regulation, but the mechanisms underlying the formation of these interactions is currently unknown. In this manuscript, we investigate the molecular associations between different protein components of insulators (BEAF32, CP190 and Chromator) by biochemical and biophysical means, and develop a novel biophysical assay to determine what factors are necessary and essential for the formation of long-range DNA interactions (LRI). Importantly, we show that CP190 and Chromator are able to mediate LRIs between specifically-bound BEAF32 nucleoprotein complexes. This ability of CP190 and Chromator to establish LRI requires specific contacts between BEAF32 and their C-terminal domains, and dimerization through their N-terminal domains. In particular, the BTB/POZ domains of CP190 form a strict homodimer. We propose a general model for insulator function in which BEAF32/dCTCF/Su(HW) provide DNA specificity, whereas CP190/Chromator are responsible for the physical interactions required for long-range contacts. This network of organized, multi-layer interactions could explain the different activities of insulators, and suggest a general mechanism for how insulators may shape the organization of higher-order chromatin during cell division.

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          Identification of functional elements and regulatory circuits by Drosophila modENCODE.

          To gain insight into how genomic information is translated into cellular and developmental programs, the Drosophila model organism Encyclopedia of DNA Elements (modENCODE) project is comprehensively mapping transcripts, histone modifications, chromosomal proteins, transcription factors, replication proteins and intermediates, and nucleosome properties across a developmental time course and in multiple cell lines. We have generated more than 700 data sets and discovered protein-coding, noncoding, RNA regulatory, replication, and chromatin elements, more than tripling the annotated portion of the Drosophila genome. Correlated activity patterns of these elements reveal a functional regulatory network, which predicts putative new functions for genes, reveals stage- and tissue-specific regulators, and enables gene-expression prediction. Our results provide a foundation for directed experimental and computational studies in Drosophila and related species and also a model for systematic data integration toward comprehensive genomic and functional annotation.
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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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              Cohesin mediates transcriptional insulation by CCCTC-binding factor.

              Cohesin complexes mediate sister-chromatid cohesion in dividing cells but may also contribute to gene regulation in postmitotic cells. How cohesin regulates gene expression is not known. Here we describe cohesin-binding sites in the human genome and show that most of these are associated with the CCCTC-binding factor (CTCF), a zinc-finger protein required for transcriptional insulation. CTCF is dispensable for cohesin loading onto DNA, but is needed to enrich cohesin at specific binding sites. Cohesin enables CTCF to insulate promoters from distant enhancers and controls transcription at the H19/IGF2 (insulin-like growth factor 2) locus. This role of cohesin seems to be independent of its role in cohesion. We propose that cohesin functions as a transcriptional insulator, and speculate that subtle deficiencies in this function contribute to 'cohesinopathies' such as Cornelia de Lange syndrome.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS Genet
                PLoS Genet
                plos
                plosgen
                PLoS Genetics
                Public Library of Science (San Francisco, USA )
                1553-7390
                1553-7404
                August 2014
                28 August 2014
                : 10
                : 8
                : e1004544
                Affiliations
                [1 ]Centre National de la Recherche Scientifique, Unité Mixte de Recherche 5048, Centre de Biochimie Structurale, Montpellier, France
                [2 ]Institut National de la Santé et la Recherche Médicale, Unité 1054, Montpellier, France
                [3 ]Universités Montpellier I et II, Montpellier, France
                [4 ]Laboratoire de Biologie Moléculaire Eucaryote, CNRS and Université de Toulouse, Toulouse; France
                [5 ]Laboratoire Diversité, Génomes & Interactions Microorganismes-Insectes, INRA UMR1333, Université de Montpellier 2, Montpellier, France
                Max Planck Institute of Immunobiology and Epigenetics, Germany
                Author notes

                The authors have declared that no competing interests exist.

                Conceived and designed the experiments: JV ALG OC GL MCG EM MN. Performed the experiments: JV ALG SD FA. Analyzed the data: JV ALG FA AG NN. Contributed reagents/materials/analysis tools: JV ALG SD OC NN. Wrote the paper: JV ALG MN.

                Article
                PGENETICS-D-13-03406
                10.1371/journal.pgen.1004544
                4148193
                25165871
                4194f377-5208-4df4-b008-fcef12fc2bb2
                Copyright @ 2014

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 12 December 2013
                : 17 June 2014
                Page count
                Pages: 17
                Funding
                Financial support was provided by European Research Council Starting Grant 260787 (MN). We also thank the French National Research Agency grant (ANR-2010-BLAN-1221 01 to OC, MN, and EM), the France-BioImaging infrastructure (ANR-10-INSB-04) and the French Infrastructure for Integrated Structural Biology (ANR-10-INSB-05-01). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology and Life Sciences
                Biochemistry
                Nucleic Acids
                Biophysics
                Cell Biology
                Chromosome Biology
                Computational Biology
                Genome Analysis
                Genome-Wide Association Studies
                Genetics
                Epigenetics
                Gene Expression
                Genomics

                Genetics
                Genetics

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