Evidence map›Paper›PMID 29972301›Full record

ArticleJournal of proteome research2018

HyPR-MS for Multiplexed Discovery of MALAT1, NEAT1, and NORAD lncRNA Protein Interactomes.

Michele Spiniello, Rachel A Knoener, Maisie I Steinbrink, Bing Yang, Anthony J Cesnik, Katherine E Buxton, Mark Scalf, David F Jarrard, Lloyd M Smith

Open access · greenAbstract read
In one paragraph

Article in Journal of proteome research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

39 citing papers in PubMed, 68 citations in OpenAlex.

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  18. Expression ofMolecular therapy. Nucleic acids · 2023
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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

9 authors at 1 institution in 1 country.

Michele SpinielloDepartment of Chemistry , University of Wisconsin-Madison , Madison , Wisconsin 53706 , United States.
Rachel A KnoenerDepartment of Chemistry , University of Wisconsin-Madison , Madison , Wisconsin 53706 , United States.ORCID 0000-0002-2787-1098
Maisie I SteinbrinkDepartment of Chemistry , University of Wisconsin-Madison , Madison , Wisconsin 53706 , United States.
Bing YangDepartment of Urology , University of Wisconsin School of Medicine and Public Health , Madison , Wisconsin 53705 , United States.
Anthony J CesnikDepartment of Chemistry , University of Wisconsin-Madison , Madison , Wisconsin 53706 , United States.ORCID 0000-0002-5326-7134
Katherine E BuxtonDepartment of Chemistry , University of Wisconsin-Madison , Madison , Wisconsin 53706 , United States.ORCID 0000-0002-0467-5983
Mark ScalfDepartment of Chemistry , University of Wisconsin-Madison , Madison , Wisconsin 53706 , United States.
David F JarrardMolecular and Environmental Toxicology , University of Wisconsin-Madison , Madison , Wisconsin 53706 , United States.
Lloyd M SmithDepartment of Chemistry , University of Wisconsin-Madison , Madison , Wisconsin 53706 , United States.
University of Wisconsin–Madison · US

Funding

Institutional Training in the Genomic SciencesT32HG002760 · NHGRI · UNIVERSITY OF WISCONSIN-MADISON · PI Qiongshi Lu · 2003 to 2026
$17.7M
Sequence-specific Hybridization Capture to Reveal the lncRNA Interactome in Prostate CancerR01CA193481 · NCI · UNIVERSITY OF WISCONSIN-MADISON · PI DAVID F. JARRARD, Lloyd M Smith · 2015 to 2026
$3.4M
NCI NIH HHS R01 CA193481NHGRI NIH HHS T32 HG002760
6 · The paper itself

Abstract

RNA-protein interactions are integral to the regulation of gene expression. RNAs have diverse functions and the protein interactomes of individual RNAs vary temporally, spatially, and with physiological context. These factors make the global acquisition of individual RNA-protein interactomes an essential endeavor. Although techniques have been reported for discovery of the protein interactomes of specific RNAs they are largely laborious, costly, and accomplished singly in individual experiments. We developed HyPR-MS for the discovery and analysis of the protein interactomes of multiple RNAs in a single experiment while also reducing design time and improving efficiencies. Presented here is the application of HyPR-MS to simultaneously and selectively isolate the interactomes of lncRNAs MALAT1, NEAT1, and NORAD. Our analysis features the proteins that potentially contribute to both known and previously undiscovered roles of each lncRNA. This platform provides a powerful new multiplexing tool for the efficient and cost-effective elucidation of specific RNA-protein interactomes.

Indexed as

Base SequenceCell Line, TumorGene Expression RegulationGene OntologyHumansMass SpectrometryMolecular Sequence AnnotationProtein BindingProteomicsRNA-Binding ProteinsRNA, Long NoncodingMALAT1 long non-coding RNA, humanNEAT1 long non-coding RNA, humanNORAD long non-coding RNA, humanRNA-Binding ProteinsRNA, Long Noncodinghybridization captureinteractomeslncRNAmass spectrometryproteomicsRNARNA-binding proteins

Identifiers

PMID29972301
PMCPMC6425737
OpenAlexW2810359426

What OpenQuestion holds

Textmetadata
LicenceTDM
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.