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dc.contributor.authorRicci-Tam, Chiara
dc.contributor.authorHua, Bo
dc.contributor.authorSpringer, Michael
dc.contributor.authorBrennan, Christopher M
dc.contributor.authorMoomau, Christine Anne
dc.contributor.authorHsu, Pei-Hsin
dc.contributor.authorSilberman, Rebecca Estelle
dc.contributor.authorAmon, Angelika B.
dc.contributor.authorThorburn, Rebecca Ruth
dc.date.accessioned2018-06-06T18:12:34Z
dc.date.available2018-06-06T18:12:34Z
dc.date.issued2017-04
dc.date.submitted2016-12
dc.identifier.issn0092-8674
dc.identifier.issn1097-4172
dc.identifier.urihttp://hdl.handle.net/1721.1/116147
dc.description.abstractPhenotypic variability is a hallmark of diseases involving chromosome gains and losses, such as Down syndrome and cancer. Allelic variances have been thought to be the sole cause of this heterogeneity. Here, we systematically examine the consequences of gaining and losing single or multiple chromosomes to show that the aneuploid state causes non-genetic phenotypic variability. Yeast cell populations harboring the same defined aneuploidy exhibit heterogeneity in cell-cycle progression and response to environmental perturbations. Variability increases with degree of aneuploidy and is partly due to gene copy number imbalances, suggesting that subtle changes in gene expression impact the robustness of biological networks and cause alternate behaviors when they occur across many genes. As inbred trisomic mice also exhibit variable phenotypes, we further propose that non-genetic individuality is a universal characteristic of the aneuploid state that may contribute to variability in presentation and treatment responses of diseases caused by aneuploidy. Keywords: aneuploidy; non-genetic heterogeneity; cell-to-cell variability; gene dosage effects; biological noise; Down syndrome; canceren_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant CA206157)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant GM118066)en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (Grant DGE1122374)en_US
dc.publisherElsevier BVen_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/J.CELL.2017.03.021en_US
dc.rightsCreative Commons Attribution-NonCommercial-NoDerivs Licenseen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.sourcePMCen_US
dc.titleAneuploidy Causes Non-genetic Individualityen_US
dc.typeArticleen_US
dc.identifier.citationBeach, Rebecca R. et al. “Aneuploidy Causes Non-Genetic Individuality.” Cell 169, 2 (April 2017): 229–242 © 2017 Elsevier Incen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.contributor.mitauthorBeach, Rebecca Ruth
dc.contributor.mitauthorBrennan, Christopher M
dc.contributor.mitauthorMoomau, Christine Anne
dc.contributor.mitauthorHsu, Pei-Hsin
dc.contributor.mitauthorSilberman, Rebecca Estelle
dc.contributor.mitauthorAmon, Angelika B.
dc.relation.journalCellen_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
dc.date.updated2018-06-05T16:43:34Z
dspace.orderedauthorsBeach, Rebecca R.; Ricci-Tam, Chiara; Brennan, Christopher M.; Moomau, Christine A.; Hsu, Pei-hsin; Hua, Bo; Silberman, Rebecca E.; Springer, Michael; Amon, Angelikaen_US
dspace.embargo.termsNen_US
dc.identifier.orcidhttps://orcid.org/0000-0002-2345-5038
dc.identifier.orcidhttps://orcid.org/0000-0002-9399-7174
dc.identifier.orcidhttps://orcid.org/0000-0002-9342-5678
dc.identifier.orcidhttps://orcid.org/0000-0001-8026-1777
dc.identifier.orcidhttps://orcid.org/0000-0002-5655-2176
mit.licensePUBLISHER_CCen_US


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