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dc.contributor.authorDileep, Vishnu
dc.contributor.authorMcCord, Rachel Patton
dc.contributor.authorDekker, Job
dc.contributor.authorGilbert, David M.
dc.date2022-08-11T08:09:53.000
dc.date.accessioned2022-08-23T16:47:47Z
dc.date.available2022-08-23T16:47:47Z
dc.date.issued2019-07-09
dc.date.submitted2019-08-09
dc.identifier.citation<p>Stem Cell Reports. 2019 Jul 9;13(1):193-206. doi: 10.1016/j.stemcr.2019.05.021. Epub 2019 Jun 20. <a href="https://doi.org/10.1016/j.stemcr.2019.05.021">Link to article on publisher's site</a></p>
dc.identifier.issn2213-6711 (Linking)
dc.identifier.doi10.1016/j.stemcr.2019.05.021
dc.identifier.pmid31231024
dc.identifier.urihttp://hdl.handle.net/20.500.14038/41147
dc.description<p>Full author list omitted for brevity. For the full list of authors, see article.</p>
dc.description.abstractThe temporal order of DNA replication is regulated during development and is highly correlated with gene expression, histone modifications and 3D genome architecture. We tracked changes in replication timing, gene expression, and chromatin conformation capture (Hi-C) A/B compartments over the first two cell cycles during differentiation of human embryonic stem cells to definitive endoderm. Remarkably, transcriptional programs were irreversibly reprogrammed within the first cell cycle and were largely but not universally coordinated with replication timing changes. Moreover, changes in A/B compartment and several histone modifications that normally correlate strongly with replication timing showed weak correlation during the early cell cycles of differentiation but showed increased alignment in later differentiation stages and in terminally differentiated cell lines. Thus, epigenetic cell fate transitions during early differentiation can occur despite dynamic and discordant changes in otherwise highly correlated genomic properties.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=31231024&dopt=Abstract">Link to Article in PubMed</a></p>
dc.rightsCopyright 2019 The Author(s). This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectchromatin 3D architecture
dc.subjectchromatin 3D organization
dc.subjectchromatin structure
dc.subjectdifferentiation
dc.subjectgene expression
dc.subjectlineage commitment
dc.subjectreplication timing
dc.subjectAmino Acids, Peptides, and Proteins
dc.subjectBiochemistry
dc.subjectCell and Developmental Biology
dc.subjectCells
dc.subjectCellular and Molecular Physiology
dc.subjectEmbryonic Structures
dc.subjectGenetic Phenomena
dc.subjectMolecular Biology
dc.subjectStructural Biology
dc.titleRapid Irreversible Transcriptional Reprogramming in Human Stem Cells Accompanied by Discordance between Replication Timing and Chromatin Compartment
dc.typeJournal Article
dc.source.journaltitleStem cell reports
dc.source.volume13
dc.source.issue1
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=4952&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/3936
dc.identifier.contextkey15087859
refterms.dateFOA2022-08-23T16:47:47Z
html.description.abstract<p>The temporal order of DNA replication is regulated during development and is highly correlated with gene expression, histone modifications and 3D genome architecture. We tracked changes in replication timing, gene expression, and chromatin conformation capture (Hi-C) A/B compartments over the first two cell cycles during differentiation of human embryonic stem cells to definitive endoderm. Remarkably, transcriptional programs were irreversibly reprogrammed within the first cell cycle and were largely but not universally coordinated with replication timing changes. Moreover, changes in A/B compartment and several histone modifications that normally correlate strongly with replication timing showed weak correlation during the early cell cycles of differentiation but showed increased alignment in later differentiation stages and in terminally differentiated cell lines. Thus, epigenetic cell fate transitions during early differentiation can occur despite dynamic and discordant changes in otherwise highly correlated genomic properties.</p>
dc.identifier.submissionpathoapubs/3936
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology
dc.contributor.departmentProgram in Systems Biology
dc.source.pages193-206


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Copyright 2019 The Author(s).  This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
Except where otherwise noted, this item's license is described as Copyright 2019 The Author(s). This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).