Evidence map›Paper›PMID 24782528›Full record

ArticleNucleic acids research2014

The interaction of MYC with the trithorax protein ASH2L promotes gene transcription by regulating H3K27 modification.

Andrea Ullius, Juliane Lüscher-Firzlaff, Ivan G Costa, Gesa Walsemann, Alexandra H Forst, Eduardo G Gusmao, Karsten Kapelle, Henning Kleine, Elisabeth Kremmer, Jörg Vervoorts and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

43 citing papers in PubMed, 59 citations in OpenAlex.

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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

11 authors at 2 institutions in 1 country.

Andrea UlliusInstitute of Biochemistry and Molecular Biology, Medical School, RWTH Aachen University, 52074 Aachen, Germany.
Juliane Lüscher-FirzlaffInstitute of Biochemistry and Molecular Biology, Medical School, RWTH Aachen University, 52074 Aachen, Germany.
Ivan G CostaIZKF Research Group Computational Biology, Medical School, RWTH Aachen University, 52074 Aachen, Germany.
Gesa WalsemannInstitute of Biochemistry and Molecular Biology, Medical School, RWTH Aachen University, 52074 Aachen, Germany.
Alexandra H ForstInstitute of Biochemistry and Molecular Biology, Medical School, RWTH Aachen University, 52074 Aachen, Germany.
Eduardo G GusmaoIZKF Research Group Computational Biology, Medical School, RWTH Aachen University, 52074 Aachen, Germany.
Karsten KapelleInstitute of Biochemistry and Molecular Biology, Medical School, RWTH Aachen University, 52074 Aachen, Germany.
Henning KleineInstitute of Biochemistry and Molecular Biology, Medical School, RWTH Aachen University, 52074 Aachen, Germany.
Elisabeth KremmerHelmholtz Zentrum München, Institut für Molekulare Immunologie, Marchioninistr. 25, 81377 München, Germany.
Jörg VervoortsInstitute of Biochemistry and Molecular Biology, Medical School, RWTH Aachen University, 52074 Aachen, Germany jvervoorts-weber@ukaachen.de.
Bernhard LüscherInstitute of Biochemistry and Molecular Biology, Medical School, RWTH Aachen University, 52074 Aachen, Germany Luescher@rwth-aachen.de.
RWTH Aachen University · DEHelmholtz Zentrum München · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The appropriate expression of the roughly 30,000 human genes requires multiple layers of control. The oncoprotein MYC, a transcriptional regulator, contributes to many of the identified control mechanisms, including the regulation of chromatin, RNA polymerases, and RNA processing. Moreover, MYC recruits core histone-modifying enzymes to DNA. We identified an additional transcriptional cofactor complex that interacts with MYC and that is important for gene transcription. We found that the trithorax protein ASH2L and MYC interact directly in vitro and co-localize in cells and on chromatin. ASH2L is a core subunit of KMT2 methyltransferase complexes that target histone H3 lysine 4 (H3K4), a mark associated with open chromatin. Indeed, MYC associates with H3K4 methyltransferase activity, dependent on the presence of ASH2L. MYC does not regulate this methyltransferase activity but stimulates demethylation and subsequently acetylation of H3K27. KMT2 complexes have been reported to associate with histone H3K27-specific demethylases, while CBP/p300, which interact with MYC, acetylate H3K27. Finally WDR5, another core subunit of KMT2 complexes, also binds directly to MYC and in genome-wide analyses MYC and WDR5 are associated with transcribed promoters. Thus, our findings suggest that MYC and ASH2L-KMT2 complexes cooperate in gene transcription by controlling H3K27 modifications and thereby regulate bivalent chromatin.

Indexed as

Gene Expression RegulationTranscription, GeneticCell LineDNA-Binding ProteinsHistone-Lysine N-MethyltransferaseHistonesHumansIntracellular Signaling Peptides and ProteinsMethylationNuclear ProteinsPromoter Regions, GeneticProto-Oncogene Proteins c-mycTranscription FactorsASH2L protein, humanDNA-Binding ProteinsHistone-Lysine N-MethyltransferaseHistonesIntracellular Signaling Peptides and ProteinsNuclear ProteinsProto-Oncogene Proteins c-mycTranscription FactorsWDR5 protein, human

Identifiers

PMID24782528
PMCPMC4066752
OpenAlexW2071965536

What OpenQuestion holds

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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.