A large-scale binding and functional map of human RNA-binding proteins

Eric L. Van Nostrand(University of California San Diego), Peter Freese(Massachusetts Institute of Technology), Henry Pratt(University of California San Diego), Xiaofeng Wang(Montreal Clinical Research Institute), Xintao Wei(Institute for Systems Biology), Rui Xiao(University of California San Diego), Steven M. Blue(University of California San Diego), Jiayu Chen(University of California San Diego), Neal Cody(Montreal Clinical Research Institute), Daniel Domínguez(Massachusetts Institute of Technology), Sara Olson(Institute for Systems Biology), Balaji Sundararaman(University of California San Diego), Lijun Zhan(Institute for Systems Biology), Cassandra Bazile(Massachusetts Institute of Technology), Louis Philip Benoit Bouvrette(Montreal Clinical Research Institute), Julie Bergalet(Montreal Clinical Research Institute), Michael O. Duff(Institute for Systems Biology), Keri E. Garcia(University of California San Diego), Chelsea Gelboin-Burkhart(University of California San Diego), Myles Hochman(Massachusetts Institute of Technology), Nicole Lambert(Massachusetts Institute of Technology), Hairi Li(University of California San Diego), Michael P. McGurk(Massachusetts Institute of Technology), Thai B. Nguyen(University of California San Diego), Tsultrim Palden(Massachusetts Institute of Technology), Ines Rabano(University of California San Diego), Shashank Sathe(University of California San Diego), Rebecca Stanton(University of California San Diego), Amanda Su(Massachusetts Institute of Technology), Ruth Wang(University of California San Diego), Brian A. Yee(University of California San Diego), Bing Zhou(University of California San Diego), Ashley L. Louie(University of California San Diego), Stefan Aigner(University of California San Diego), Xiang‐Dong Fu(University of California San Diego), Éric Lécuyer(Montreal Clinical Research Institute), Christopher B. Burge(Massachusetts Institute of Technology), Brenton R. Graveley(Institute for Systems Biology), G Yeo(University of California San Diego)
Nature
July 29, 2020
Cited by 1,364Open Access
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Abstract

. 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.


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