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dc.contributor.authorUhler, Caroline
dc.contributor.authorShivashankar, G.V.
dc.date.accessioned2021-03-11T21:56:50Z
dc.date.available2021-03-11T21:56:50Z
dc.date.issued2017-11
dc.identifier.issn0962-8924
dc.identifier.urihttps://hdl.handle.net/1721.1/130126
dc.description.abstractCells sense physical and chemical signals from their local microenvironment and transduce them to the nucleus to regulate genomic programs. In this review, we first discuss different modes of mechanotransduction to the nucleus. Then we highlight the role of the spatial organization of chromosomes for integrating these signals. In particular, we emphasize the importance of chromosome intermingling for gene regulation. We also discuss various geometric models and recent advances in microscopy and genomics that have allowed accessing these nanoscale chromosome intermingling regions. Taken together, the recent work summarized in this review culminates in the hypothesis that the chromosome intermingling regions are mechanical hotspots for genome regulation. Maintenance of such mechanical hotspots is crucial for cellular homeostasis, and alterations in them could be precursors for various cellular reprogramming events including diseases.en_US
dc.description.sponsorshipDARPA (Contract W911NF-16-1-0551)en_US
dc.description.sponsorshipNSF (Grant DMS-1651995)en_US
dc.description.sponsorshipONR (Grant N00014-17-1-2147)en_US
dc.publisherElsevier BVen_US
dc.relation.isversionofhttps://doi.org/10.1016/j.tcb.2017.06.005en_US
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourceProf. Uhler via Phoebe Ayersen_US
dc.titleChromosome Intermingling: Mechanical Hotspots for Genome Regulationen_US
dc.typeArticleen_US
dc.identifier.citationUhler, Caroline and G.V. Shivashankar. "Chromosome Intermingling: Mechanical Hotspots for Genome Regulation." Trends in Cell Biology 27, 11 (November 2017): P810-819. © 2017 Elsevier Ltden_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Scienceen_US
dc.contributor.departmentMassachusetts Institute of Technology. Institute for Data, Systems, and Societyen_US
dc.relation.journalTrends in Cell Biologyen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.date.submission2021-03-05T17:40:21Z
mit.journal.volume27en_US
mit.journal.issue11en_US
mit.licensePUBLISHER_CC
mit.metadata.statusComplete


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