Evidence map›Paper›PMID 15520282›Full record

ArticleGenes & development2004

The Polycomb Ezh2 methyltransferase regulates muscle gene expression and skeletal muscle differentiation.

Giuseppina Caretti, Monica Di Padova, Bruce Micales, Gary E Lyons, Vittorio Sartorelli

Erratum issuedOpen access · diamondAbstract read
In one paragraph

Article in Genes & development, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 359 papers.

0numbers the graph read from it
0cells of the map it votes in
359citing 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

359 citing papers in PubMed, 605 citations in OpenAlex.

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  10. The role of inner nuclear membrane protein emerin in myogenesis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
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  15. An epigenetic memory at thebioRxiv : the preprint server for biology · 2024
    Article
  16. Review
  17. Muscle-specific pyruvate kinase isoforms, PKM1 and PKM2, regulate mammalian SWI/SNF proteins and histone 3 phosphorylation during myoblast differentiation.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article
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299 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

5 authors at 3 institutions in 1 country.

Giuseppina CarettiMuscle Gene Expression Group, Laboratory of Muscle Biology, NIAMS, National Institutes of Health, Bethesda, Maryland 20892, USA.
Monica Di Padova
Bruce Micales
Gary E Lyons
Vittorio Sartorelli
National Institutes of Health · USUniversity of Wisconsin–Madison · USProtein Express (United States) · US

Funding

Control of Myogenesis and Regulation of MyoD Post-Transcriptional ModificationsZIAAR041126 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI SARTORELLI, VITTORIO · 2009 to 2025
$28.7M
REGULATION OF MYOD POST TRANSCRIPTIONAL MODIFICATIONSZ01AR041126 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI SARTORELLI, VITTORIO · 2000 to 2008
$2.4M
6 · The paper itself

Abstract

The Ezh2 protein endows the Polycomb PRC2 and PRC3 complexes with histone lysine methyltransferase (HKMT) activity that is associated with transcriptional repression. We report that Ezh2 expression was developmentally regulated in the myotome compartment of mouse somites and that its down-regulation coincided with activation of muscle gene expression and differentiation of satellite-cell-derived myoblasts. Increased Ezh2 expression inhibited muscle differentiation, and this property was conferred by its SET domain, required for the HKMT activity. In undifferentiated myoblasts, endogenous Ezh2 was associated with the transcriptional regulator YY1. Both Ezh2 and YY1 were detected, with the deacetylase HDAC1, at genomic regions of silent muscle-specific genes. Their presence correlated with methylation of K27 of histone H3. YY1 was required for Ezh2 binding because RNA interference of YY1 abrogated chromatin recruitment of Ezh2 and prevented H3-K27 methylation. Upon gene activation, Ezh2, HDAC1, and YY1 dissociated from muscle loci, H3-K27 became hypomethylated and MyoD and SRF were recruited to the chromatin. These findings suggest the existence of a two-step activation mechanism whereby removal of H3-K27 methylation, conferred by an active Ezh2-containing protein complex, followed by recruitment of positive transcriptional regulators at discrete genomic loci are required to promote muscle gene expression and cell differentiation.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsCell DifferentiationChromatinDNA-Binding ProteinsEnhancer of Zeste Homolog 2 ProteinErythroid-Specific DNA-Binding FactorsExtremitiesHistone Deacetylase 1Histone DeacetylasesHistone-Lysine N-MethyltransferaseLysineMethylationMethyltransferasesMiceMice, Inbred StrainsChromatinDNA-Binding ProteinsEnhancer of Zeste Homolog 2 ProteinErythroid-Specific DNA-Binding FactorsEzh2 protein, mouseHdac1 protein, mouseHistone Deacetylase 1Histone DeacetylasesHistone-Lysine N-MethyltransferaseLysineMethyltransferasesMyoD ProteinPolycomb Repressive Complex 2ProteinsRNA, Small InterferingSerum Response FactorTranscription FactorsYy1 protein, mouseYY1 Transcription Factor

Identifiers

PMID15520282
PMCPMC525543
OpenAlexW2108136318

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.