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

Author

Listed:
  • Eric L. Nostrand

    (University of California San Diego
    University of California San Diego)

  • Peter Freese

    (Massachusetts Institute of Technology)

  • Gabriel A. Pratt

    (University of California San Diego
    University of California San Diego
    University of California San Diego)

  • Xiaofeng Wang

    (Institut de Recherches Cliniques de Montréal (IRCM))

  • Xintao Wei

    (Institute for Systems Genomics, UConn Health)

  • Rui Xiao

    (University of California San Diego
    University of California San Diego
    Wuhan University)

  • Steven M. Blue

    (University of California San Diego
    University of California San Diego)

  • Jia-Yu Chen

    (University of California San Diego
    University of California San Diego)

  • Neal A. L. Cody

    (Institut de Recherches Cliniques de Montréal (IRCM))

  • Daniel Dominguez

    (Massachusetts Institute of Technology)

  • Sara Olson

    (Institute for Systems Genomics, UConn Health)

  • Balaji Sundararaman

    (University of California San Diego
    University of California San Diego)

  • Lijun Zhan

    (Institute for Systems Genomics, UConn Health)

  • Cassandra Bazile

    (Massachusetts Institute of Technology)

  • Louis Philip Benoit Bouvrette

    (Institut de Recherches Cliniques de Montréal (IRCM)
    Université de Montréal)

  • Julie Bergalet

    (Institut de Recherches Cliniques de Montréal (IRCM))

  • Michael O. Duff

    (Institute for Systems Genomics, UConn Health)

  • Keri E. Garcia

    (University of California San Diego
    University of California San Diego)

  • Chelsea Gelboin-Burkhart

    (University of California San Diego
    University of California San Diego)

  • Myles Hochman

    (Massachusetts Institute of Technology)

  • Nicole J. Lambert

    (Massachusetts Institute of Technology)

  • Hairi Li

    (University of California San Diego
    University of California San Diego)

  • Michael P. McGurk

    (Massachusetts Institute of Technology)

  • Thai B. Nguyen

    (University of California San Diego
    University of California San Diego)

  • Tsultrim Palden

    (Massachusetts Institute of Technology
    Massachusetts Institute of Technology)

  • Ines Rabano

    (University of California San Diego
    University of California San Diego)

  • Shashank Sathe

    (University of California San Diego
    University of California San Diego)

  • Rebecca Stanton

    (University of California San Diego
    University of California San Diego)

  • Amanda Su

    (Massachusetts Institute of Technology)

  • Ruth Wang

    (University of California San Diego
    University of California San Diego)

  • Brian A. Yee

    (University of California San Diego
    University of California San Diego)

  • Bing Zhou

    (University of California San Diego
    University of California San Diego)

  • Ashley L. Louie

    (University of California San Diego
    University of California San Diego)

  • Stefan Aigner

    (University of California San Diego
    University of California San Diego)

  • Xiang-Dong Fu

    (University of California San Diego
    University of California San Diego)

  • Eric Lécuyer

    (Institut de Recherches Cliniques de Montréal (IRCM)
    Université de Montréal
    McGill University)

  • Christopher B. Burge

    (Massachusetts Institute of Technology
    Massachusetts Institute of Technology
    Massachusetts Institute of Technology)

  • Brenton R. Graveley

    (Institute for Systems Genomics, UConn Health)

  • Gene W. Yeo

    (University of California San Diego
    University of California San Diego
    University of California San Diego)

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.

Suggested Citation

  • Eric L. Nostrand & Peter Freese & Gabriel A. Pratt & Xiaofeng Wang & Xintao Wei & Rui Xiao & Steven M. Blue & Jia-Yu Chen & Neal A. L. Cody & Daniel Dominguez & Sara Olson & Balaji Sundararaman & Liju, 2020. "A large-scale binding and functional map of human RNA-binding proteins," Nature, Nature, vol. 583(7818), pages 711-719, July.
  • Handle: RePEc:nat:nature:v:583:y:2020:i:7818:d:10.1038_s41586-020-2077-3
    DOI: 10.1038/s41586-020-2077-3
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