Evidence map›Paper›PMID 32252787›Full record

ArticleGenome biology2020

Principles of RNA processing from analysis of enhanced CLIP maps for 150 RNA binding proteins.

Eric L Van Nostrand, Gabriel A Pratt, Brian A Yee, Emily C Wheeler, Steven M Blue, Jasmine Mueller, Samuel S Park, Keri E Garcia, Chelsea Gelboin-Burkhart, Thai B Nguyen and 7 more

Open access · goldAbstract read
In one paragraph

Article in Genome biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 146 papers.

0numbers the graph read from it
0cells of the map it votes in
146citing papers in PubMed
11.5field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

146 citing papers in PubMed, 244 citations in OpenAlex.

  1. Article
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  10. Detection of a sequence feature for recursive splicing.bioRxiv : the preprint server for biology · 2026
    Article
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  16. Allele-specific splicing modulates protein isoforms and Alzheimer's risk.bioRxiv : the preprint server for biology · 2026
    Article
  17. Article
  18. Review
  19. Article
  20. Article

86 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors at 2 institutions in 1 country.

Eric L Van NostrandDepartment of Cellular and Molecular Medicine, University of California San Diego, La Jolla, CA, USA.
Gabriel A PrattDepartment of Cellular and Molecular Medicine, University of California San Diego, La Jolla, CA, USA.
Brian A YeeDepartment of Cellular and Molecular Medicine, University of California San Diego, La Jolla, CA, USA.
Emily C WheelerDepartment of Cellular and Molecular Medicine, University of California San Diego, La Jolla, CA, USA.
Steven M BlueDepartment of Cellular and Molecular Medicine, University of California San Diego, La Jolla, CA, USA.
Jasmine MuellerDepartment of Cellular and Molecular Medicine, University of California San Diego, La Jolla, CA, USA.
Samuel S ParkDepartment of Cellular and Molecular Medicine, University of California San Diego, La Jolla, CA, USA.
Keri E GarciaDepartment of Cellular and Molecular Medicine, University of California San Diego, La Jolla, CA, USA.
Chelsea Gelboin-BurkhartDepartment of Cellular and Molecular Medicine, University of California San Diego, La Jolla, CA, USA.
Thai B NguyenDepartment of Cellular and Molecular Medicine, University of California San Diego, La Jolla, CA, USA.
Ines RabanoDepartment of Cellular and Molecular Medicine, University of California San Diego, La Jolla, CA, USA.
Rebecca StantonDepartment of Cellular and Molecular Medicine, University of California San Diego, La Jolla, CA, USA.
Balaji SundararamanDepartment of Cellular and Molecular Medicine, University of California San Diego, La Jolla, CA, USA.
Ruth WangDepartment of Cellular and Molecular Medicine, University of California San Diego, La Jolla, CA, USA.
Xiang-Dong FuDepartment of Cellular and Molecular Medicine, University of California San Diego, La Jolla, CA, USA.
Brenton R GraveleyDepartment of Genetics and Genome Sciences, Institute for Systems Genomics, UConn Health, Farmington, CT, USA. graveley@uchc.edu.
Gene W YeoDepartment of Cellular and Molecular Medicine, University of California San Diego, La Jolla, CA, USA. geneyeo@ucsd.edu.
University of California, San Diego · USInstitute for Systems Biology · US

Funding

Comprhensive analysis of functional RNA elements encoded in the human genomeU54HG007005 · NHGRI · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI GRAVELEY, BRENTON R. · 2012 to 2017
$12.5M
Functional RNA elements in the human genomeR01HG004659 · NHGRI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Kevin Daniel Corbett, Eugene Wei-Ming Yeo · 2008 to 2026
$12.4M
A Comprehensive Functional Map of Human Protein-RNA InteractionsU41HG009889 · NHGRI · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI GRAVELEY, BRENTON R., YEO, EUGENE WEI-MING · 2018 to 2021
$9.4M
Training Program in Basic Clinical GeneticsT32GM008666 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HAMILTON, BRUCE A · 1998 to 2021
$8.6M
Robust, high-throughput identification of RNA processing regulators and regulatory networks genome-wideR00HG009530 · NHGRI · BAYLOR COLLEGE OF MEDICINE · PI VAN NOSTRAND, ERIC LYMAN · 2020 to 2022
$747k
Robust, high-throughput identification of RNA processing regulators and regulatory networks genome-wideK99HG009530 · NHGRI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI VAN NOSTRAND, ERIC LYMAN · 2017 to 2018
$250k
NHGRI NIH HHS K99 HG009530NHGRI NIH HHS R00 HG009530NHGRI NIH HHS U54 HG007005
6 · The paper itself

Abstract

backgroundA critical step in uncovering rules of RNA processing is to study the in vivo regulatory networks of RNA binding proteins (RBPs). Crosslinking and immunoprecipitation (CLIP) methods enable mapping RBP targets transcriptome-wide, but methodological differences present challenges to large-scale analysis across datasets. The development of enhanced CLIP (eCLIP) enabled the mapping of targets for 150 RBPs in K562 and HepG2, creating a unique resource of RBP interactomes profiled with a standardized methodology in the same cell types.

resultsOur analysis of 223 eCLIP datasets reveals a range of binding modalities, including highly resolved positioning around splicing signals and mRNA untranslated regions that associate with distinct RBP functions. Quantification of enrichment for repetitive and abundant multicopy elements reveals 70% of RBPs have enrichment for non-mRNA element classes, enables identification of novel ribosomal RNA processing factors and sites, and suggests that association with retrotransposable elements reflects multiple RBP mechanisms of action. Analysis of spliceosomal RBPs indicates that eCLIP resolves AQR association after intronic lariat formation, enabling identification of branch points with single-nucleotide resolution, and provides genome-wide validation for a branch point-based scanning model for 3' splice site recognition. Finally, we show that eCLIP peak co-occurrences across RBPs enable the discovery of novel co-interacting RBPs.

conclusionsThis work reveals novel insights into RNA biology by integrated analysis of eCLIP profiling of 150 RBPs with distinct functions. Further, our quantification of both mRNA and other element association will enable further research to identify novel roles of RBPs in regulating RNA processing.

Indexed as

RNA Processing, Post-TranscriptionalBinding SitesHep G2 CellsHumansImmunoprecipitationIntronsK562 CellsRepetitive Sequences, Nucleic AcidRetroelementsRNARNA-Binding ProteinsRNA, RibosomalRNA SplicingSpliceosomesRetroelementsRNARNA-Binding ProteinsRNA, RibosomalCLIP-seqeCLIPRNA binding proteinRNA processing

Identifiers

PMID32252787
PMCPMC7137325
OpenAlexW3014747614

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.