Evidence map›Paper›PMID 26177152›Full record

ArticleRNA biology2015

Cryptic RNA-binding by PRC2 components EZH2 and SUZ12.

Juan G Betancur, Yukihide Tomari

Open access · bronzeAbstract read
In one paragraph

Article in RNA biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

19 citing papers in PubMed, 28 citations in OpenAlex.

  1. Phosphorylation event changes the RNA binding mode of EZH2 disordered segment.Protein science : a publication of the Protein Society · 2026
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  17. RNA-mediated regulation of heterochromatin.Current opinion in cell biology · 2017
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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

2 authors at 2 institutions in 3 countries.

Juan G Betancura Institute of Molecular and Cellular Biosciences; The University of Tokyo ; Bunkyo-ku, Tokyo , Japan.
Yukihide Tomaria Institute of Molecular and Cellular Biosciences; The University of Tokyo ; Bunkyo-ku, Tokyo , Japan.
Institut thématique Génétique, génomique et bioinformatique · FRThe University of Tokyo · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polycomb repressive complex 2 (PRC2) is a histone-modifying complex that di/tri-methylates histone H3 lysine 27 (H3K27), a mark of transcriptionally repressed chromatin. However, how PRC2 is specifically recruited to its target loci remains controversial, although it has been postulated that long non-coding RNAs (lncRNAs) can function as guides. Here we purified individual components of PRC2 from human cultured cells and found that EZH2 and SUZ12 can directly bind to RNAs. In agreement with recent evidence, our results support the notion that these two PRC2 subunits have RNA-binding activity, with general preference for longer RNAs. However, the length alone does not explain their cryptic substrate preference. Our data highlight the difficulty of characterizing the RNA-binding activity of PRC2.

Indexed as

Enhancer of Zeste Homolog 2 ProteinHumansNeoplasm ProteinsPolycomb Repressive Complex 2Protein BindingRNARNA-Binding ProteinsRNA, Long NoncodingTranscription FactorsEnhancer of Zeste Homolog 2 ProteinEZH2 protein, humanNeoplasm ProteinsPolycomb Repressive Complex 2RNARNA-Binding ProteinsRNA, Long NoncodingSUZ12 protein, humanTranscription FactorsEZH2HOTAIRlncRNAPRC2SUZ12Xist

Identifiers

PMID26177152
PMCPMC4615636
OpenAlexW1941097672

What OpenQuestion holds

Textmetadata
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.