A Large-Scale Binding and Functional Map of Human RNA Binding Proteins
Eric L. Van NostrandiD, Peter Freese, Henry PrattiD, Xiaofeng WangiD, Xintao Wei, Rui XiaoiD, Steven M. BlueiD, Jiayu CheniD, Neal A. L. Cody, Daniel Dominguez, Sara OlsoniD, Balaji SundararamaniD, Lijun ZhaniD, Cassandra A BazileiD, Louis Philip Benoit BouvretteiD, Julie Bergalet, Michael O. DuffiD, Keri E. Garcia, Chelsea Anne Gelboin-Burkhart, Myles HochmaniD, Nicole J. Lambert, Hairi Li, Michael P. McGurkiD, Thai B. NguyeniD, Tsultrim Palden, , Gene Wei-Ming YeoiD
Abstract
Genomes encompass all the information necessary to specify the development and function of an organism. In addition to genes, genomes also contain a myriad of functional elements that control various steps in gene expression. A major class of these elements function only when transcribed into RNA as they serve as the binding sites for RNA binding proteins (RBPs), which act to control post-transcriptional processes including splicing, cleavage and polyadenylation, RNA editing, RNA localization, stability, and translation. Despite the importance of these functional RNA elements encoded in the genome, they have been much less studied than genes and DNA elements. Here, we describe the mapping and characterization of RNA elements recognized by a large collection of human RBPs in K562 and HepG2 cells. These data expand the catalog of functional elements encoded in the human genome by addition of a large set of elements that function at the RNA level through interaction with RBPs.\n\nHighlightsO_LI223 eCLIP datasets for 150 RBPs reveal a wide variety of in vivo RNA target classes.\nC_LIO_LI472 knockdown/RNA-seq profiles of 263 RBPs reveal factor-responsive targets and integration with eCLIP indicates RNA expression and splicing regulatory patterns.\nC_LIO_LI78 RNA Bind-N-Seq profiles of in vitro binding motifs reveal links between in vitro and in vivo binding and indicate that eCLIP peaks that contain in vitro motifs are more strongly associated with regulation.\nC_LIO_LI274 maps of RBP subcellular localization by immunofluorescence indicate widespread organelle-specific RNA processing regulation.\nC_LIO_LI63 ChIP-seq profiles of DNA association suggest broad interconnectivity between chromatin association and RNA processing.\nC_LI
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 1,314
- FWCI
- 50.10
- Field percentile
- top 1%
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Principles of RNA processing from analysis of enhanced CLIP maps for 150 RNA binding proteins.
Eric L. Van Nostrand, Gabriel A. Pratt, … Gene Wei-Ming Yeo·Genome biologyPeer-reviewed·Apr 6, 2020
- Deciphering human ribonucleoprotein regulatory networks
Neelanjan Mukherjee, Hans‐Hermann Wessels, … Uwe Ohler·Nucleic Acids ResearchPeer-reviewed·Nov 26, 2018
- Binding patterns of RNA binding proteins to repeat-derived RNA sequences reveal putative functional RNA elements
Masahiro Onoguchi, Chao Zeng, … Michiaki Hamada·NAR Genomics and BioinformaticsPeer-reviewed·Jun 23, 2021
- A gene set collection of RBP target genes
Markus Glaß, Stefan Hüttelmaier·bioRxiv·Oct 14, 2025
- irCLIP-RNP and Re-CLIP reveal patterns of dynamic protein associations on RNA
Luca Ducoli, Brian J. Zarnegar, … Paul A. Khavari·NaturePeer-reviewed·Mar 26, 2025
- Modeling RNA-binding protein specificity in vivo by precisely registering protein-RNA crosslink sites
Huijuan Feng, Suying Bao, … Chaolin Zhang·Molecular CellPeer-reviewed·Jun 1, 2019