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dc.contributor.authorFreese, Peter Dale
dc.contributor.authorDominguez, Daniel
dc.contributor.authorBazile, Cassandra
dc.contributor.authorHochman, Myles
dc.contributor.authorLambert, Nicole
dc.contributor.authorMcGurk, Michael P.
dc.contributor.authorPalden, Tsultrim
dc.contributor.authorSu, Amanda J
dc.contributor.authorBurge, Christopher B
dc.date.accessioned2021-10-27T20:23:35Z
dc.date.available2021-10-27T20:23:35Z
dc.date.issued2020
dc.identifier.urihttps://hdl.handle.net/1721.1/135470
dc.description.abstract© 2020, The Author(s). Many proteins regulate the expression of genes by binding to specific regions encoded in the genome1. Here we introduce a new data set of RNA elements in the human genome that are recognized by RNA-binding proteins (RBPs), generated as part of the Encyclopedia of DNA Elements (ENCODE) project phase III. This class of regulatory elements functions only when transcribed into RNA, as they serve as the binding sites for RBPs that control post-transcriptional processes such as splicing, cleavage and polyadenylation, and the editing, localization, stability and translation of mRNAs. We describe the mapping and characterization of RNA elements recognized by a large collection of human RBPs in K562 and HepG2 cells. Integrative analyses using five assays identify RBP binding sites on RNA and chromatin in vivo, the in vitro binding preferences of RBPs, the function of RBP binding sites and the subcellular localization of RBPs, producing 1,223 replicated data sets for 356 RBPs. We describe the spectrum of RBP binding throughout the transcriptome and the connections between these interactions and various aspects of RNA biology, including RNA stability, splicing regulation and RNA localization. These data expand the catalogue of functional elements encoded in the human genome by the addition of a large set of elements that function at the RNA level by interacting with RBPs.
dc.language.isoen
dc.publisherSpringer Science and Business Media LLC
dc.relation.isversionof10.1038/S41586-020-2077-3
dc.rightsCreative Commons Attribution 4.0 International license
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.sourceNature
dc.titleA large-scale binding and functional map of human RNA-binding proteins
dc.typeArticle
dc.contributor.departmentMassachusetts Institute of Technology. Computational and Systems Biology Program
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biology
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineering
dc.relation.journalNature
dc.eprint.versionFinal published version
dc.type.urihttp://purl.org/eprint/type/JournalArticle
eprint.statushttp://purl.org/eprint/status/PeerReviewed
dc.date.updated2021-07-14T16:38:40Z
dspace.orderedauthorsVan Nostrand, EL; Freese, P; Pratt, GA; Wang, X; Wei, X; Xiao, R; Blue, SM; Chen, J-Y; Cody, NAL; Dominguez, D; Olson, S; Sundararaman, B; Zhan, L; Bazile, C; Bouvrette, LPB; Bergalet, J; Duff, MO; Garcia, KE; Gelboin-Burkhart, C; Hochman, M; Lambert, NJ; Li, H; McGurk, MP; Nguyen, TB; Palden, T; Rabano, I; Sathe, S; Stanton, R; Su, A; Wang, R; Yee, BA; Zhou, B; Louie, AL; Aigner, S; Fu, X-D; Lécuyer, E; Burge, CB; Graveley, BR; Yeo, GW
dspace.date.submission2021-07-14T16:38:50Z
mit.journal.volume583
mit.journal.issue7818
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Needed


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