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dc.contributor.authorWroblewska, Liliana
dc.contributor.authorDuportet, Xavier
dc.contributor.authorGuye, Patrick
dc.contributor.authorLi, Yinqing
dc.contributor.authorWeiss, Ron
dc.contributor.authorEyquem, Justin
dc.contributor.authorRieders, Julianne
dc.contributor.authorRimchala, Tharathorn
dc.contributor.authorBatt, Gregory
dc.date.accessioned2014-12-29T19:41:15Z
dc.date.available2014-12-29T19:41:15Z
dc.date.issued2014-11
dc.date.submitted2014-09
dc.identifier.issn0305-1048
dc.identifier.issn1362-4962
dc.identifier.urihttp://hdl.handle.net/1721.1/92532
dc.description.abstractMammalian synthetic biology may provide novel therapeutic strategies, help decipher new paths for drug discovery and facilitate synthesis of valuable molecules. Yet, our capacity to genetically program cells is currently hampered by the lack of efficient approaches to streamline the design, construction and screening of synthetic gene networks. To address this problem, here we present a framework for modular and combinatorial assembly of functional (multi)gene expression vectors and their efficient and specific targeted integration into a well-defined chromosomal context in mammalian cells. We demonstrate the potential of this framework by assembling and integrating different functional mammalian regulatory networks including the largest gene circuit built and chromosomally integrated to date (6 transcription units, 27kb) encoding an inducible memory device. Using a library of 18 different circuits as a proof of concept, we also demonstrate that our method enables one-pot/single-flask chromosomal integration and screening of circuit libraries. This rapid and powerful prototyping platform is well suited for comparative studies of genetic regulatory elements, genes and multi-gene circuits as well as facile development of libraries of isogenic engineered cell lines.en_US
dc.description.sponsorshipNational Institute of General Medical Sciences (U.S.) (P50GM098792)en_US
dc.description.sponsorshipFrance. Agence nationale de la recherche (Syne2arti. ANR-10-COSINUS-007)en_US
dc.description.sponsorshipFrance. Agence nationale de la recherche (Iceberg. ANR-IABI-3096)en_US
dc.description.sponsorshipUnited States. Defense Advanced Research Projects Agency (Controlling Cellular Machinery. R0011–12-C-0067)en_US
dc.description.sponsorshipUnited States. Defense Advanced Research Projects Agency (Synbio BBN. DARPA-BAA-11–23)en_US
dc.language.isoen_US
dc.publisherOxford University Pressen_US
dc.relation.isversionofhttp://dx.doi.org/10.1093/nar/gku1082en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0en_US
dc.sourceOxford University Pressen_US
dc.titleA platform for rapid prototyping of synthetic gene networks in mammalian cellsen_US
dc.typeArticleen_US
dc.identifier.citationDuportet, Xavier, Liliana Wroblewska, Patrick Guye, Yingqing Li, Justin Eyquem, Julianne Rieders, Tharathorn Rimchala, Gregory Batt, and Ron Weiss. “A Platform for Rapid Prototyping of Synthetic Gene Networks in Mammalian Cells.” Nucleic Acids Research 42, no. 21 (November 5, 2014): 13440–13451.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Scienceen_US
dc.contributor.departmentMassachusetts Institute of Technology. Synthetic Biology Centeren_US
dc.contributor.mitauthorWroblewska, Lilianaen_US
dc.contributor.mitauthorGuye, Patricken_US
dc.contributor.mitauthorLi, Yinqingen_US
dc.contributor.mitauthorWeiss, Ronen_US
dc.contributor.mitauthorRimchala, Tharathornen_US
dc.relation.journalNucleic Acids Researchen_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.orderedauthorsDuportet, Xavier; Wroblewska, Liliana; Guye, Patrick; Li, Yingqing; Eyquem, Justin; Rieders, Julianne; Rimchala, Tharathorn; Batt, Gregory; Weiss, Ronen_US
dc.identifier.orcidhttps://orcid.org/0000-0003-0396-2443
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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