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      Emerging Evidence of Chromosome Folding by Loop Extrusion

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          Abstract

          Chromosome organization poses a remarkable physical problem with many biological consequences: How can molecular interactions between proteins at the nanometer scale organize micron-long chromatinized DNA molecules, insulating or facilitating interactions between specific genomic elements? The mechanism of active loop extrusion holds great promise for explaining interphase and mitotic chromosome folding, yet remains difficult to assay directly. We discuss predictions from our polymer models of loop extrusion with barrier elements and review recent experimental studies that provide strong support for loop extrusion, focusing on perturbations to CTCF and cohesin assayed via Hi-C in interphase. Finally, we discuss a likely molecular mechanism of loop extrusion by structural maintenance of chromosomes complexes.

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          Most cited references55

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          Organization of the mitotic chromosome.

          Mitotic chromosomes are among the most recognizable structures in the cell, yet for over a century their internal organization remains largely unsolved. We applied chromosome conformation capture methods, 5C and Hi-C, across the cell cycle and revealed two distinct three-dimensional folding states of the human genome. We show that the highly compartmentalized and cell type-specific organization described previously for nonsynchronous cells is restricted to interphase. In metaphase, we identified a homogenous folding state that is locus-independent, common to all chromosomes, and consistent among cell types, suggesting a general principle of metaphase chromosome organization. Using polymer simulations, we found that metaphase Hi-C data are inconsistent with classic hierarchical models and are instead best described by a linearly organized longitudinally compressed array of consecutive chromatin loops.
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            Genome-wide dynamics of Pol II elongation and its interplay with promoter proximal pausing, chromatin, and exons

            Production of mRNA depends critically on the rate of RNA polymerase II (Pol II) elongation. To dissect Pol II dynamics in mouse ES cells, we inhibited Pol II transcription at either initiation or promoter-proximal pause escape with Triptolide or Flavopiridol, and tracked Pol II kinetically using GRO-seq. Both inhibitors block transcription of more than 95% of genes, showing that pause escape, like initiation, is a ubiquitous and crucial step within the transcription cycle. Moreover, paused Pol II is relatively stable, as evidenced from half-life measurements at ∼3200 genes. Finally, tracking the progression of Pol II after drug treatment establishes Pol II elongation rates at over 1000 genes. Notably, Pol II accelerates dramatically while transcribing through genes, but slows at exons. Furthermore, intergenic variance in elongation rates is substantial, and is influenced by a positive effect of H3K79me2 and negative effects of exon density and CG content within genes. DOI: http://dx.doi.org/10.7554/eLife.02407.001
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              CTCF establishes discrete functional chromatin domains at the Hox clusters during differentiation.

              Polycomb and Trithorax group proteins encode the epigenetic memory of cellular positional identity by establishing inheritable domains of repressive and active chromatin within the Hox clusters. Here we demonstrate that the CCCTC-binding factor (CTCF) functions to insulate these adjacent yet antagonistic chromatin domains during embryonic stem cell differentiation into cervical motor neurons. Deletion of CTCF binding sites within the Hox clusters results in the expansion of active chromatin into the repressive domain. CTCF functions as an insulator by organizing Hox clusters into spatially disjoint domains. Ablation of CTCF binding disrupts topological boundaries such that caudal Hox genes leave the repressed domain and become subject to transcriptional activation. Hence, CTCF is required to insulate facultative heterochromatin from impinging euchromatin to produce discrete positional identities.
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                Author and article information

                Journal
                1256107
                3100
                Cold Spring Harb Symp Quant Biol
                Cold Spring Harb. Symp. Quant. Biol.
                Cold Spring Harbor symposia on quantitative biology
                0091-7451
                1943-4456
                26 April 2019
                04 May 2018
                2017
                13 May 2019
                : 82
                : 45-55
                Affiliations
                [1 ]Gladstone Institute of Data Science and Technology, University of California, San Francisco, California 94158
                [2 ]Computational and Systems Biology Program, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139
                [3 ]Institute for Medical Engineering and Science (IMES), Massachusetts Institute of Technology, Cambridge, Massachusetts 02139
                [4 ]Department of Physics, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139
                [5 ]These authors contributed equally to this work.
                Author notes
                Article
                NIHMS1012011
                10.1101/sqb.2017.82.034710
                6512960
                29728444
                8d709d06-c797-49b6-a5f1-8b3b1bd6fecd

                This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted reuse and redistribution provided that the original author and source are credited.

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