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dc.creatorWellensiek, BP
dc.creatorLarsen, AC
dc.creatorStephens, B
dc.creatorKukurba, K
dc.creatorWaern, K
dc.creatorBriones, N
dc.creatorLiu, L
dc.creatorSnyder, M
dc.creatorJacobs, BL
dc.creatorKumar, S
dc.creatorChaput, JC
dc.date.accessioned2021-02-04T19:42:40Z
dc.date.available2021-02-04T19:42:40Z
dc.date.issued2013-08-01
dc.identifier.issn1548-7091
dc.identifier.issn1548-7105
dc.identifier.doihttp://dx.doi.org/10.34944/dspace/5937
dc.identifier.other23770754 (pubmed)
dc.identifier.urihttp://hdl.handle.net/20.500.12613/5955
dc.description.abstractWe report an in vitro selection strategy to identify RNA sequences that mediate cap-independent initiation of translation. This method entails mRNA display of trillions of genomic fragments, selection for initiation of translation and high-throughput deep sequencing. We identified >12,000 translation-enhancing elements (TEEs) in the human genome, generated a high-resolution map of human TEE-bearing regions (TBRs), and validated the function of a subset of sequences in vitro and in cultured cells. © 2013 Nature America, Inc. All rights reserved.
dc.format.extent747-750
dc.language.isoen
dc.relation.haspartNature Methods
dc.relation.isreferencedbySpringer Science and Business Media LLC
dc.subject5' Untranslated Regions
dc.subjectGene Library
dc.subjectGenome, Human
dc.subjectHeLa Cells
dc.subjectHigh-Throughput Nucleotide Sequencing
dc.subjectHumans
dc.subjectPeptide Chain Initiation, Translational
dc.subjectProtein Biosynthesis
dc.subjectRNA, Messenger
dc.titleGenome-wide profiling of human cap-independent translation-enhancing elements
dc.typeArticle
dc.type.genreJournal Article
dc.relation.doi10.1038/nmeth.2522
dc.ada.noteFor Americans with Disabilities Act (ADA) accommodation, including help with reading this content, please contact scholarshare@temple.edu
dc.creator.orcidKumar, Sudhir|0000-0002-9918-8212
dc.date.updated2021-02-04T19:42:37Z
refterms.dateFOA2021-02-04T19:42:41Z


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