| Literature DB >> 32728246 |
Eric L Van Nostrand1,2, Peter Freese3, Gabriel A Pratt1,2,4, Xiaofeng Wang5, Xintao Wei6, Rui Xiao1,2,7, Steven M Blue1,2, Jia-Yu Chen1,2, Neal A L Cody5, Daniel Dominguez8, Sara Olson6, Balaji Sundararaman1,2, Lijun Zhan6, Cassandra Bazile8, Louis Philip Benoit Bouvrette5,9, Julie Bergalet5, Michael O Duff6, Keri E Garcia1,2, Chelsea Gelboin-Burkhart1,2, Myles Hochman8, Nicole J Lambert8, Hairi Li1,2, Michael P McGurk8, Thai B Nguyen1,2, Tsultrim Palden8,10, Ines Rabano1,2, Shashank Sathe1,2, Rebecca Stanton1,2, Amanda Su8, Ruth Wang1,2, Brian A Yee1,2, Bing Zhou1,2, Ashley L Louie1,2, Stefan Aigner1,2, Xiang-Dong Fu11,12, Eric Lécuyer13,14,15, Christopher B Burge16,17,18, Brenton R Graveley19, Gene W Yeo20,21,22.
Abstract
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.Entities:
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Year: 2020 PMID: 32728246 PMCID: PMC7410833 DOI: 10.1038/s41586-020-2077-3
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962