Evidence map›Paper›PMID 32220894›Full record

ArticleRNA (New York, N.Y.)2020

RNA-GPS predicts high-resolution RNA subcellular localization and highlights the role of splicing.

Kevin E Wu, Kevin R Parker, Furqan M Fazal, Howard Y Chang, James Zou

Open access · bronzeAbstract read
In one paragraph

Article in RNA (New York, N.Y.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

17 citing papers in PubMed, 23 citations in OpenAlex.

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  13. Illuminating lncRNA Function Through Target Prediction.Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  14. Review
  15. Article
  16. Article
  17. Subcellular Spatial Transcriptomes: Emerging Frontier for Understanding Gene Regulation.Cold Spring Harbor symposia on quantitative biology · 2019
    Article
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

5 authors at 2 institutions in 1 country.

Kevin E WuDepartment of Computer Science, Stanford University, Stanford, California 94305, USA.ORCID 0000-0002-4786-9796
Kevin R ParkerCenter for Personal and Dynamic Regulomes, Stanford University School of Medicine, Stanford, California 94305, USA.
Furqan M FazalCenter for Personal and Dynamic Regulomes, Stanford University School of Medicine, Stanford, California 94305, USA.ORCID 0000-0003-0758-4582
Howard Y ChangCenter for Personal and Dynamic Regulomes, Stanford University School of Medicine, Stanford, California 94305, USA.
James ZouDepartment of Computer Science, Stanford University, Stanford, California 94305, USA.
Stanford University · USHoward Hughes Medical Institute · US

Funding

INSTITUTIONAL TRAINING GRANT IN GENOME SCIENCET32HG000044 · NHGRI · STANFORD UNIVERSITY · PI MICHAEL P. SNYDER · 1995 to 2026
$32.2M
Center for Personal Dynamic RegulomesRM1HG007735 · NHGRI · STANFORD UNIVERSITY · PI CHANG, HOWARD Y · 2019 to 2023
$13.8M
Stanford Medicine Center for Longevity and Healthy Aging Research Education CoreP30AG059307 · NIA · STANFORD UNIVERSITY · PI PERIYAKOIL, VYJEYANTHI S · 2018 to 2025
$4.9M
Structural Motifs in RNAR01HG004361 · NHGRI · STANFORD UNIVERSITY · PI CHANG, HOWARD Y · 2007 to 2018
$4.7M
Revealing Principles of Subcellular RNA Localization by Proximity LabelingR00HG010910 · NHGRI · BAYLOR COLLEGE OF MEDICINE · PI FAZAL, FURQAN · 2021 to 2023
$747k
Developing data tools to reduce CVD disparities via Health Information ExchangesR21MD012867 · NIMHD · STANFORD UNIVERSITY · PI ZOU, JAMES · 2018 to 2019
$420k
Revealing Principles of Subcellular RNA Localization by Proximity LabelingK99HG010910 · NHGRI · STANFORD UNIVERSITY · PI FAZAL, FURQAN · 2019 to 2020
$223k
Howard Hughes Medical InstituteNHGRI NIH HHS K99 HG010910NHGRI NIH HHS R00 HG010910NHGRI NIH HHS R01 HG004361NHGRI NIH HHS RM1 HG007735NHGRI NIH HHS T32 HG000044NIA NIH HHS P30 AG059307NIMHD NIH HHS R21 MD012867
6 · The paper itself

Abstract

Subcellular localization is essential to RNA biogenesis, processing, and function across the gene expression life cycle. However, the specific nucleotide sequence motifs that direct RNA localization are incompletely understood. Fortunately, new sequencing technologies have provided transcriptome-wide atlases of RNA localization, creating an opportunity to leverage computational modeling. Here we present RNA-GPS, a new machine learning model that uses nucleotide-level features to predict RNA localization across eight different subcellular locations-the first to provide such a wide range of predictions. RNA-GPS's design enables high-throughput sequence ablation and feature importance analyses to probe the sequence motifs that drive localization prediction. We find localization informative motifs to be concentrated on 3'-UTRs and scattered along the coding sequence, and motifs related to splicing to be important drivers of predicted localization, even for cytotopic distinctions for membraneless bodies within the nucleus or for organelles within the cytoplasm. Overall, our results suggest transcript splicing is one of many elements influencing RNA subcellular localization.

Indexed as

3' Untranslated RegionsAlternative SplicingCell Line, TumorCell NucleusComputational BiologyCytoplasmHeLa CellsHumansK562 CellsRNASequence Analysis, RNATranscriptome3' Untranslated RegionsRNAlocalization mechanismmachine learning modelRNA localizationsplicing in localization

Identifiers

PMID32220894
PMCPMC7297119
OpenAlexW3013900099

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.