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dc.contributor.authorTorres, Eduardo Martin
dc.contributor.authorDephoure, Noah
dc.contributor.authorPanneerselvam, Amudha
dc.contributor.authorTucker, Cheryl M.
dc.contributor.authorWhittaker, Charles A.
dc.contributor.authorGygi, Steven P.
dc.contributor.authorDunham, Maitreya J.
dc.contributor.authorAmon, Angelika B
dc.date.accessioned2013-12-19T16:12:34Z
dc.date.available2013-12-19T16:12:34Z
dc.date.issued2010-10
dc.date.submitted2010-06
dc.identifier.issn00928674
dc.identifier.issn1097-4172
dc.identifier.urihttp://hdl.handle.net/1721.1/82940
dc.description.abstractAneuploidy causes a proliferative disadvantage in all normal cells analyzed to date, yet this condition is associated with a disease characterized by unabated proliferative potential, cancer. The mechanisms that allow cancer cells to tolerate the adverse effects of aneuploidy are not known. To probe this question, we identified aneuploid yeast strains with improved proliferative abilities. Their molecular characterization revealed strain-specific genetic alterations as well as mutations shared between different aneuploid strains. Among the latter, a loss-of-function mutation in the gene encoding the deubiquitinating enzyme Ubp6 improves growth rates in four different aneuploid yeast strains by attenuating the changes in intracellular protein composition caused by aneuploidy. Our results demonstrate the existence of aneuploidy-tolerating mutations that improve the fitness of multiple different aneuploidies and highlight the importance of ubiquitin-proteasomal degradation in suppressing the adverse effects of aneuploidy.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (grant P50 GM071508)en_US
dc.description.sponsorshipCharles A. King Trust (Postdoctoral Research Fellowship Program)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (grant GM56800)en_US
dc.language.isoen_US
dc.publisherElsevier B.V.en_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.cell.2010.08.038en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceElsevier Open Archiveen_US
dc.titleIdentification of Aneuploidy-Tolerating Mutationsen_US
dc.typeArticleen_US
dc.identifier.citationTorres, Eduardo M., Noah Dephoure, Amudha Panneerselvam, Cheryl M. Tucker, Charles A. Whittaker, Steven P. Gygi, Maitreya J. Dunham, and Angelika Amon. “Identification of Aneuploidy-Tolerating Mutations.” Cell 143, no. 1 (October 2010): 71-83. © 2010 Elsevier Inc.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.contributor.mitauthorTorres, Eduardo Martinen_US
dc.contributor.mitauthorPanneerselvam, Amudhaen_US
dc.contributor.mitauthorWhittaker, Charles A.en_US
dc.contributor.mitauthorAmon, Angelika B.en_US
dc.relation.journalCellen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsTorres, Eduardo M.; Dephoure, Noah; Panneerselvam, Amudha; Tucker, Cheryl M.; Whittaker, Charles A.; Gygi, Steven P.; Dunham, Maitreya J.; Amon, Angelikaen_US
dc.identifier.orcidhttps://orcid.org/0000-0001-9837-0314
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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