{"ID": "PMID:29217590", "lab": {"@type": ["Lab", "Item"], "uuid": "82ebab19-8a20-47c5-baeb-9a08a9524b10", "display_title": "Leonid Mirny, MIT", "title": "Leonid Mirny, MIT", "correspondence": [{"contact_email": "bGVvbmlkQG1pdC5lZHU=", "@id": "/users/f520d12a-e4c4-4774-a230-08d6dc4f5ef1/", "display_title": "Leonid Mirny"}], "@id": "/labs/leonid-mirny-lab/", "status": "current", "pi": {"error": "no view permissions"}, "principals_allowed": {"view": ["system.Everyone"], "edit": ["group.admin", "role.lab_submitter", "submits_for.82ebab19-8a20-47c5-baeb-9a08a9524b10"]}}, "url": "https://www.ncbi.nlm.nih.gov/pubmed/29217590", "award": {"name": "1U54DK107980-01", "status": "current", "description": "NOFIC: The spatial organization of the genome impinges on all genomic processes, including gene regulation, maintenance of genome stability and chromosome transmission to daughter cells. A detailed understanding of the spatial arrangement of the human genome, referred to as the 4D nucleome, and the biological and physical principles that drive chromosome folding requires combining approaches from the fields of molecular and cell biology, imaging, genetics and genomics with approaches from physics, computational biology, and computer simulation. We have assembled a highly interdisciplinary center with the goal of generating extensively validated maps of the 4D nucleome, its physical and dynamic properties and its role in regulating the activity of the genome. First, the center will further optimize and extensively validate a suite of genome-wide molecular methodologies, based on chromosome conformation capture (3C) that can probe the folding of chromosomes at the scale of single nucleosomes, chromatin fibers, chromosomes and the entire nucleus, across cell populations and in single cells. Given that chromosome and nuclear organization is tightly linked to biological state of the cell, the center will map the 4D nucleome for four key biological states representing different conformations during the cell cycle (interphase and mitosis), and during cell differentiation (pluripotent and differentiated states). We will obtain complementary data regarding the structure and dynamics of chromatin, at different length scales and in single cells using extensive high-throughput imaging, live cell imaging and super resolution microscopy. Data obtained with all approaches will be analyzed, integrated and modeled using a set of methods we will further develop to gain insights into the structure, physics and dynamics of chromosome folding over different length scales. Finally, a critical component of our proposal is the biological validation and further elaboration of the chromatin interaction maps that are generated from our conformational analyses. This validation will be achieved through site-specific editing of genomic sequence and epigenetic marks, the creation of new contact points within the genome, and the identification of factors (both protein and nucleic acid) that facilitat or restrict these interactions. Effects of such perturbations in the chromosome conformation on transcription will reveal relationships between specific chromosome structural features and gene expression.", "display_title": "CENTER FOR 3D STRUCTURE AND PHYSICS OF THE GENOME", "uuid": "ae6c618f-7a8c-441e-a886-e30bbbe591da", "center_title": "NOFIC - Dekker", "@id": "/awards/1U54DK107980-01/", "project": "4DN", "@type": ["Award", "Item"], "pi": {"error": "no view permissions"}, "principals_allowed": {"view": ["system.Everyone"], "edit": ["group.admin"]}}, "title": "A mechanism of cohesin-dependent loop extrusion organizes zygotic genome architecture.", "status": "current", "aliases": ["mirny-lab:gassler_et_al_2017"], "authors": ["Gassler J", "Brandao HB", "Imakaev M", "Flyamer IM", "Ladstatter S", "Bickmore WA", "Peters JM", "Mirny LA", "Tachibana K"], "journal": "The EMBO journal", "abstract": "Fertilization triggers assembly of higher-order chromatin structure from a condensed maternal and a naive paternal genome to generate a totipotent embryo. Chromatin loops and domains have been detected in mouse zygotes by single-nucleus Hi-C (snHi-C), but not bulk Hi-C. It is therefore unclear when and how embryonic  chromatin conformations are assembled. Here, we investigated whether a mechanism  of cohesin-dependent loop extrusion generates higher-order chromatin structures within the one-cell embryo. Using snHi-C of mouse knockout embryos, we demonstrate that the zygotic genome folds into loops and domains that critically  depend on Scc1-cohesin and that are regulated in size and linear density by Wapl. Remarkably, we discovered distinct effects on maternal and paternal chromatin loop sizes, likely reflecting differences in loop extrusion dynamics and epigenetic reprogramming. Dynamic polymer models of chromosomes reproduce changes in snHi-C, suggesting a mechanism where cohesin locally compacts chromatin by active loop extrusion, whose processivity is controlled by Wapl. Our simulations  and experimental data provide evidence that cohesin-dependent loop extrusion organizes mammalian genomes over multiple scales from the one-cell embryo onward.", "date_created": "2018-06-14T18:14:37.169817+00:00", "submitted_by": {"error": "no view permissions"}, "last_modified": {"modified_by": {"error": "no view permissions"}, "date_modified": "2018-08-30T18:55:55.987282+00:00"}, "date_published": "2017-12-07", "public_release": "2018-08-30", "schema_version": "2", "exp_sets_prod_in_pub": [{"@id": "/experiment-set-replicates/4DNESJ5VTYV3/", "status": "released", "accession": "4DNESJ5VTYV3", "experimentset_type": "replicate", "@type": ["ExperimentSetReplicate", "ExperimentSet", "Item"], "uuid": "2cc72872-b596-4395-b733-d796d51469e7", "display_title": "4DNESJ5VTYV3", "experiments_in_set": [{"status": "released", "@type": ["ExperimentHiC", "Experiment", "Item"], "display_title": "sn-Hi-C on animal zygote with DpnII - 4DNEXDXHL1TR", "@id": "/experiments-hi-c/4DNEXDXHL1TR/", "uuid": "b271e3a8-6a66-4cbb-a6ec-65343a9bb9ae", "principals_allowed": {"view": ["system.Everyone"], "edit": ["group.admin"]}, "experiment_type": {"@id": "/experiment-types/sn-hi-c/", "display_title": "sn-Hi-C", "@type": ["ExperimentType", "Item"], "status": "released", "uuid": "7a0f628b-cf79-4ac9-8f03-77a1f9c73ed7", "title": "sn-Hi-C", "principals_allowed": {"view": ["system.Everyone"], "edit": ["group.admin"]}}}], "principals_allowed": {"view": ["system.Everyone"], "edit": ["group.admin"]}}, {"@id": "/experiment-set-replicates/4DNES3IAVK94/", "status": "released", "accession": "4DNES3IAVK94", "experimentset_type": "replicate", "@type": ["ExperimentSetReplicate", "ExperimentSet", "Item"], "uuid": "36f88f27-2870-4c0a-90a9-a9a2dce8d37b", "display_title": "4DNES3IAVK94", "experiments_in_set": [{"status": "released", "@type": ["ExperimentHiC", "Experiment", "Item"], "display_title": "sn-Hi-C on animal zygote with DpnII - 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