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dc.contributor.authorBumgarner, Stacie L.
dc.contributor.authorNeuert, Gregor
dc.contributor.authorVoight, Benjamin F.
dc.contributor.authorSymbor-Nagrabska, Anna
dc.contributor.authorGrisafi, Paula
dc.contributor.authorvan Oudenaarden, Alexander
dc.contributor.authorFink, Gerald R.
dc.contributor.authorvan Oudenaarden, Alexander
dc.date.accessioned2014-01-08T16:46:05Z
dc.date.available2014-01-08T16:46:05Z
dc.date.issued2012-02
dc.date.submitted2011-10
dc.identifier.issn10972765
dc.identifier.issn1097-4164
dc.identifier.urihttp://hdl.handle.net/1721.1/83593
dc.description.abstractMechanisms through which long intergenic noncoding RNAs (ncRNAs) exert regulatory effects on eukaryotic biological processes remain largely elusive. Most studies of these phenomena rely on methods that measure average behaviors in cell populations, lacking resolution to observe the effects of ncRNA transcription on gene expression in a single cell. Here, we combine quantitative single-molecule RNA FISH experiments with yeast genetics and computational modeling to gain mechanistic insights into the regulation of the Saccharomyces cerevisiae protein-coding gene FLO11 by two intergenic ncRNAs, ICR1 and PWR1. Direct detection of FLO11 mRNA and these ncRNAs in thousands of individual cells revealed alternative expression states and provides evidence that ICR1 and PWR1 contribute to FLO11's variegated transcription, resulting in Flo11-dependent phenotypic heterogeneity in clonal cell populations by modulating recruitment of key transcription factors to the FLO11 promoter.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (grant M035010)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (grant GM40266)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (grant P1OD00393636)en_US
dc.description.sponsorshipNational Science Foundation (U.S.) (grant ECCS-0835623)en_US
dc.description.sponsorshipDeutsche Forschungsgemeinschaft (Forschungs Stipendium)en_US
dc.description.sponsorshipAmerican Cancer Society (Professor)en_US
dc.language.isoen_US
dc.publisherElsevier B.V.en_US
dc.relation.isversionofhttp://dx.doi.org/10.1016/j.molcel.2011.11.029en_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.titleSingle-Cell Analysis Reveals that Noncoding RNAs Contribute to Clonal Heterogeneity by Modulating Transcription Factor Recruitmenten_US
dc.typeArticleen_US
dc.identifier.citationBumgarner, Stacie L., Gregor Neuert, Benjamin F. Voight, Anna Symbor-Nagrabska, Paula Grisafi, Alexander van Oudenaarden, and Gerald R. Fink. “Single-Cell Analysis Reveals that Noncoding RNAs Contribute to Clonal Heterogeneity by Modulating Transcription Factor Recruitment.” Molecular Cell 45, no. 4 (February 2012): 470-482. © 2012 Elsevier.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Physicsen_US
dc.contributor.departmentWhitehead Institute for Biomedical Researchen_US
dc.contributor.mitauthorBumgarner, Stacie L.en_US
dc.contributor.mitauthorNeuert, Gregoren_US
dc.contributor.mitauthorSymbor-Nagrabska, Annaen_US
dc.contributor.mitauthorGrisafi, Paulaen_US
dc.contributor.mitauthorvan Oudenaarden, Alexanderen_US
dc.contributor.mitauthorFink, Gerald R.en_US
dc.relation.journalMolecular 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.orderedauthorsBumgarner, Stacie L.; Neuert, Gregor; Voight, Benjamin F.; Symbor-Nagrabska, Anna; Grisafi, Paula; van Oudenaarden, Alexander; Fink, Gerald R.en_US
dc.identifier.orcidhttps://orcid.org/0000-0003-3704-2899
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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