Evidence map›Paper›PMID 34654832›Full record

ArticleNature communications2021

Photoactivatable ribonucleosides mark base-specific RNA-binding sites.

Jong Woo Bae, Sangtae Kim, V Narry Kim, Jong-Seo Kim

Abstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
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

18 citing papers in PubMed.

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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

4 authors.

Jong Woo BaeCenter for RNA Research, Institute for Basic Science, Seoul, 08826, Korea.ORCID 0000-0002-3185-897X
Sangtae KimSeer Inc., Redwood City, CA, 94065, USA.
V Narry KimCenter for RNA Research, Institute for Basic Science, Seoul, 08826, Korea. narrykim@snu.ac.kr.ORCID 0000-0002-3213-4965
Jong-Seo KimCenter for RNA Research, Institute for Basic Science, Seoul, 08826, Korea. jongseokim@snu.ac.kr.ORCID 0000-0002-8909-8440

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RNA-protein interaction can be captured by crosslinking and enrichment followed by tandem mass spectrometry, but it remains challenging to pinpoint RNA-binding sites (RBSs) or provide direct evidence for RNA-binding. To overcome these limitations, we here developed pRBS-ID, by incorporating the benefits of UVA-based photoactivatable ribonucleoside (PAR; 4-thiouridine and 6-thioguanosine) crosslinking and chemical RNA cleavage. pRBS-ID robustly detects peptides crosslinked to PAR adducts, offering direct RNA-binding evidence and identifying RBSs at single amino acid-resolution with base-specificity (U or G). Using pRBS-ID, we could profile uridine-contacting RBSs globally and discover guanosine-contacting RBSs, which allowed us to characterize the base-specific interactions. We also applied the search pipeline to analyze the datasets from UVC-based RBS-ID experiments, altogether offering a comprehensive list of human RBSs with high coverage (3,077 RBSs in 532 proteins in total). pRBS-ID is a widely applicable platform to investigate the molecular basis of posttranscriptional regulation.

Indexed as

Binding SitesAmino AcidsHeLa CellsHumansProtein Interaction Domains and MotifsProteomicsRibonucleosidesRNARNA-Binding ProteinsTandem Mass SpectrometryThiouridineAmino AcidsRibonucleosidesRNARNA-Binding ProteinsThiouridine

Identifiers

PMID34654832
PMCPMC8519950

What OpenQuestion holds

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LicenceCC BY
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.