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dc.contributor.authorCarey, Bryce W.
dc.contributor.authorMarkoulaki, Styliani
dc.contributor.authorHanna, Jacob
dc.contributor.authorFaddah, Dina A.
dc.contributor.authorBuganim, Yosef
dc.contributor.authorKim, Jongpil
dc.contributor.authorGanz, Kibibi
dc.contributor.authorSteine, Eveline J.
dc.contributor.authorCassady, John P.
dc.contributor.authorCreyghton, Menno P.
dc.contributor.authorWelstead, G. Grant
dc.contributor.authorGao, Qing
dc.contributor.authorJaenisch, Rudolf
dc.date.accessioned2015-03-04T19:02:11Z
dc.date.available2015-03-04T19:02:11Z
dc.date.issued2011-12
dc.date.submitted2011-11
dc.identifier.issn19345909
dc.identifier.urihttp://hdl.handle.net/1721.1/95810
dc.description.abstractWe compared two genetically highly defined transgenic systems to identify parameters affecting reprogramming of somatic cells to a pluripotent state. Our results demonstrate that the level and stoichiometry of reprogramming factors during the reprogramming process strongly influence the resulting pluripotency of iPS cells. High expression of Oct4 and Klf4 combined with lower expression of c-Myc and Sox2 produced iPS cells that efficiently generated “all-iPSC mice” by tetraploid (4n) complementation, maintained normal imprinting at the Dlk1-Dio3 locus, and did not create mice with tumors. Loss of imprinting (LOI) at the Dlk1-Dio3 locus did not strictly correlate with reduced pluripotency though the efficiency of generating “all-iPSC mice” was diminished. Our data indicate that stoichiometry of reprogramming factors can influence epigenetic and biological properties of iPS cells. This concept complicates efforts to define a “generic” epigenetic state of iPSCs and ESCs and should be considered when comparing different iPS and ES cell lines.en_US
dc.description.sponsorshipNational Science Foundation (U.S.). Graduate Research Fellowship Programen_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant 5-RO1-HDO45022)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant 5-R37-CA084198)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.). (Grant 5-RO1-CA087869)en_US
dc.language.isoen_US
dc.publisherElsevieren_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.stem.2011.11.003en_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.sourceElsevieren_US
dc.titleReprogramming Factor Stoichiometry Influences the Epigenetic State and Biological Properties of Induced Pluripotent Stem Cellsen_US
dc.typeArticleen_US
dc.identifier.citationCarey, Bryce W., Styliani Markoulaki, Jacob H. Hanna, Dina A. Faddah, Yosef Buganim, Jongpil Kim, Kibibi Ganz, et al. “Reprogramming Factor Stoichiometry Influences the Epigenetic State and Biological Properties of Induced Pluripotent Stem Cells.” Cell Stem Cell 9, no. 6 (December 2011): 588–598. © 2011 Elsevier Inc.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentWhitehead Institute for Biomedical Researchen_US
dc.contributor.mitauthorFaddah, Dina A.en_US
dc.contributor.mitauthorCarey, Bryce W.en_US
dc.contributor.mitauthorCassady, John P.en_US
dc.contributor.mitauthorJaenisch, Rudolfen_US
dc.relation.journalCell Stem Cellen_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.orderedauthorsCarey, Bryce W.; Markoulaki, Styliani; Hanna, Jacob H.; Faddah, Dina A.; Buganim, Yosef; Kim, Jongpil; Ganz, Kibibi; Steine, Eveline J.; Cassady, John P.; Creyghton, Menno P.; Welstead, G. Grant; Gao, Qing; Jaenisch, Rudolfen_US
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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