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dc.contributor.authorMukherji, Shankar
dc.contributor.authorEbert, Margaret S.
dc.contributor.authorSharp, Phillip A.
dc.contributor.authorvan Oudenaarden, Alexander
dc.contributor.authorTsang, John S.
dc.contributor.authorZheng, Xinying Grace
dc.date.accessioned2012-11-13T15:19:50Z
dc.date.available2012-11-13T15:19:50Z
dc.date.issued2011-08
dc.date.submitted2010-11
dc.identifier.issn1061-4036
dc.identifier.issn1546-1718
dc.identifier.urihttp://hdl.handle.net/1721.1/74623
dc.description.abstractMicroRNAs (miRNAs) are short, highly conserved noncoding RNA molecules that repress gene expression in a sequence-dependent manner. We performed single-cell measurements using quantitative fluorescence microscopy and flow cytometry to monitor a target gene's protein expression in the presence and absence of regulation by miRNA. We find that although the average level of repression is modest, in agreement with previous population-based measurements, the repression among individual cells varies dramatically. In particular, we show that regulation by miRNAs establishes a threshold level of target mRNA below which protein production is highly repressed. Near this threshold, protein expression responds sensitively to target mRNA input, consistent with a mathematical model of molecular titration. These results show that miRNAs can act both as a switch and as a fine-tuner of gene expression.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.). Director's Pioneer Award (1DP1OD003936)en_US
dc.description.sponsorshipNational Cancer Institute (U.S.). Physical Sciences-Oncology Center (U54CA143874)en_US
dc.description.sponsorshipUnited States. Public Health Service (Grant R01-CA133404)en_US
dc.description.sponsorshipUnited States. Public Health Service (Grant R01-GM34277)en_US
dc.description.sponsorshipNational Cancer Institute (U.S.) (PO1-CA42063)en_US
dc.description.sponsorshipNational Cancer Institute (U.S.) Cancer Center Support (Grant P30-CA14051)en_US
dc.description.sponsorshipHoward Hughes Medical Institute. Predoctoral Fellowshipen_US
dc.description.sponsorshipCleo and Paul Schimmel Foundation. Fellowshipen_US
dc.description.sponsorshipNatural Sciences and Engineering Research Council of Canada PGS Scholarshipen_US
dc.language.isoen_US
dc.publisherNature Publishing Groupen_US
dc.relation.isversionofhttp://dx.doi.org/10.1038/ng.905en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alike 3.0en_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/en_US
dc.sourcePMCen_US
dc.titleMicroRNAs can generate thresholds in target gene expressionen_US
dc.typeArticleen_US
dc.identifier.citationMukherji, Shankar et al. “MicroRNAs Can Generate Thresholds in Target Gene Expression.” Nature Genetics 43.9 (2011): 854–859.en_US
dc.contributor.departmentHarvard University--MIT Division of Health Sciences and Technologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Computational and Systems Biology Programen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Physicsen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.contributor.mitauthorMukherji, Shankar
dc.contributor.mitauthorEbert, Margaret S.
dc.contributor.mitauthorZheng, Grace X. Y.
dc.contributor.mitauthorSharp, Phillip A.
dc.contributor.mitauthorvan Oudenaarden, Alexander
dc.relation.journalNature Geneticsen_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.orderedauthorsMukherji, Shankar; Ebert, Margaret S; Zheng, Grace X Y; Tsang, John S; Sharp, Phillip A; van Oudenaarden, Alexanderen
dc.identifier.orcidhttps://orcid.org/0000-0003-1465-1691
mit.licenseOPEN_ACCESS_POLICYen_US
mit.metadata.statusComplete


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