Publication:
Genome-wide chromatin state transitions associated with developmental and environmental cues

dc.contributor.coauthorZhu, Jiang
dc.contributor.coauthorAdli, Mazhar
dc.contributor.coauthorZou, James Y.
dc.contributor.coauthorVerstappen, Griet
dc.contributor.coauthorCoyne, Michael
dc.contributor.coauthorZhang, Xiaolan
dc.contributor.coauthorDurham, Timothy
dc.contributor.coauthorMiri, Mohammad
dc.contributor.coauthorDeshpande, Vikram
dc.contributor.coauthorDe Jager, Philip L.
dc.contributor.coauthorBennett, David A.
dc.contributor.coauthorHoumard, Joseph A.
dc.contributor.coauthorMuoio, Deborah M.
dc.contributor.coauthorCamahort, Ray
dc.contributor.coauthorCowan, Chad A.
dc.contributor.coauthorMeissner, Alexander
dc.contributor.coauthorEpstein, Charles B.
dc.contributor.coauthorShoresh, Noam
dc.contributor.coauthorBernstein, Bradley E.
dc.contributor.departmentSchool of Medicine
dc.contributor.facultymemberYes
dc.contributor.kuauthorÖnder, Tamer Tevfik
dc.contributor.schoolcollegeinstituteSCHOOL OF MEDICINE
dc.date.accessioned2024-11-09T23:47:02Z
dc.date.issued2013
dc.description.abstractDifferences in chromatin organization are key to the multiplicity of cell states that arise from a single genetic background, yet the landscapes of in vivo tissues remain largely uncharted. Here, we mapped chromatin genome-wide in a large and diverse collection of human tissues and stem cells. The maps yield unprecedented annotations of functional genomic elements and their regulation across developmental stages, lineages, and cellular environments. They also reveal global features of the epigenome, related to nuclear architecture, that also vary across cellular phenotypes. Specifically, developmental specification is accompanied by progressive chromatin restriction as the default state transitions from dynamic remodeling to generalized compaction. Exposure to serum in vitro triggers a distinct transition that involves de novo establishment of domains with features of constitutive heterochromatin. We describe how these global chromatin state transitions relate to chromosome and nuclear architecture, and discuss their implications for lineage fidelity, cellular senescence, and reprogramming.
dc.description.fulltextNo
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.openaccessYES
dc.description.peerreviewstatusN/A
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipNIH Common Fund [U01 ES017155]
dc.description.sponsorshipNational Human Genome Research Institute [U54 HG004570]
dc.description.sponsorshipNational Heart, Lung and Blood Institute [U01 HL100395]
dc.description.sponsorshipNational Institute on Aging [P30 AG10161]
dc.description.sponsorshipHoward Hughes Medical Institute
dc.description.sponsorshipStarr Cancer Consortium
dc.description.sponsorshipBurroughs Wellcome Fund We acknowledge members of the Broad Institute's Epigenomics Program and Genome Sequencing and Analysis Program, and the NIH Epigenomics Mapping Consortium for constructive comments. We thank Kevin Eggan for ES and iPS lines
dc.description.sponsorshipAllen Powe and Steve Stice for neural cells
dc.description.sponsorshipGreg Lauwers and the MGH Tissue Repository for tissue procurement
dc.description.sponsorshipand David Flowers, Irwin Bernstein, John Stamatoyannopoulos and Shelly Heimfeld for blood samples. We also thank Leslie Gaffney and Lauren Solomon for assistance with figures. This research was supported by the NIH Common Fund (U01 ES017155)
dc.description.sponsorshipthe National Human Genome Research Institute (U54 HG004570)
dc.description.sponsorshipthe National Heart, Lung and Blood Institute (U01 HL100395)
dc.description.sponsorshipthe National Institute on Aging (P30 AG10161)
dc.description.sponsorshipthe Howard Hughes Medical Institute
dc.description.sponsorshipthe Starr Cancer Consortium
dc.description.sponsorshipand the Burroughs Wellcome Fund.
dc.description.studentonlypublicationNo
dc.description.studentpublicationNo
dc.description.versionN/A
dc.identifier.doi10.1016/j.cell.2012.12.033
dc.identifier.eissn1097-4172
dc.identifier.embargoN/A
dc.identifier.issn0092-8674
dc.identifier.quartileQ1
dc.identifier.scopus2-s2.0-84873310426
dc.identifier.urihttps://doi.org/10.1016/j.cell.2012.12.033
dc.identifier.urihttps://hdl.handle.net/20.500.14288/14059
dc.identifier.wos314362800031
dc.keywordsEpigenetic Signature
dc.keywordsPluripotent
dc.keywordsOrganization
dc.keywordsSenescence
dc.keywordsDynamics
dc.keywordsReveals
dc.keywordsComplex
dc.keywordsImpact
dc.keywordsGenes
dc.keywordsCells
dc.language.isoeng
dc.publisherCELL PRESS
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofCELL
dc.relation.openaccessN/A
dc.rightsN/A
dc.subjectBiochemistry
dc.subjectMolecular Biology
dc.subjectCell Biology
dc.titleGenome-wide chromatin state transitions associated with developmental and environmental cues
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorÖnder, Tamer Tevfik
relation.isOrgUnitOfPublicationd02929e1-2a70-44f0-ae17-7819f587bedd
relation.isOrgUnitOfPublication.latestForDiscoveryd02929e1-2a70-44f0-ae17-7819f587bedd
relation.isParentOrgUnitOfPublication17f2dc8e-6e54-4fa8-b5e0-d6415123a93e
relation.isParentOrgUnitOfPublication.latestForDiscovery17f2dc8e-6e54-4fa8-b5e0-d6415123a93e

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