Evidence map›Paper›PMID 25416778›Full record

ArticleThe Journal of biological chemistry2015

MEF2 transcription factors regulate distinct gene programs in mammalian skeletal muscle differentiation.

Nelsa L Estrella, Cody A Desjardins, Sarah E Nocco, Amanda L Clark, Yevgeniy Maksimenko, Francisco J Naya

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

63 citing papers in PubMed, 101 citations in OpenAlex.

  1. Article
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  3. Review
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  9. Cells · 2025
    Review
  10. Control of circadian muscle glucose metabolism through the BMAL1-HIF axis in obesity.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  11. Article
  12. Article
  13. Article
  14. The Molecular and Biological Function of MEF2D in Leukemia.Advances in experimental medicine and biology · 2024
    Review
  15. Article
  16. Article
  17. Effect of BovineGenes · 2023
    Article
  18. Review
  19. Article
  20. Article

3 more citing papers are in PubMed but not listed here.

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

6 authors at 1 institution in 1 country.

Nelsa L EstrellaFrom the Department of Biology, Program in Cell and Molecular Biology, Boston University, Boston, Massachusetts 02215.
Cody A DesjardinsFrom the Department of Biology, Program in Cell and Molecular Biology, Boston University, Boston, Massachusetts 02215.
Sarah E NoccoFrom the Department of Biology, Program in Cell and Molecular Biology, Boston University, Boston, Massachusetts 02215.
Amanda L ClarkFrom the Department of Biology, Program in Cell and Molecular Biology, Boston University, Boston, Massachusetts 02215.
Yevgeniy MaksimenkoFrom the Department of Biology, Program in Cell and Molecular Biology, Boston University, Boston, Massachusetts 02215.
Francisco J NayaFrom the Department of Biology, Program in Cell and Molecular Biology, Boston University, Boston, Massachusetts 02215 fnaya@bu.edu.
Boston University · US

Funding

Boston University Clinical and Translational Science Institute - U ProgramU54TR001012 · NCATS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI CENTER, DAVID M. · 2014 to 2014
$3.9M
MEF2 Function in Cardiac Muscle DevelopmentR01HL073304 · NHLBI · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI NAYA, FRANCISCO J · 2003 to 2013
$3.3M
NCATS NIH HHS U54 TR001012NCATS NIH HHS U54-TR001012NHLBI NIH HHS HL73304NHLBI NIH HHS HL73304-S1NHLBI NIH HHS R01 HL073304
6 · The paper itself

Abstract

Skeletal muscle differentiation requires precisely coordinated transcriptional regulation of diverse gene programs that ultimately give rise to the specialized properties of this cell type. In Drosophila, this process is controlled, in part, by MEF2, the sole member of an evolutionarily conserved transcription factor family. By contrast, vertebrate MEF2 is encoded by four distinct genes, Mef2a, -b, -c, and -d, making it far more challenging to link this transcription factor to the regulation of specific muscle gene programs. Here, we have taken the first step in molecularly dissecting vertebrate MEF2 transcriptional function in skeletal muscle differentiation by depleting individual MEF2 proteins in myoblasts. Whereas MEF2A is absolutely required for proper myoblast differentiation, MEF2B, -C, and -D were found to be dispensable for this process. Furthermore, despite the extensive redundancy, we show that mammalian MEF2 proteins regulate a significant subset of nonoverlapping gene programs. These results suggest that individual MEF2 family members are able to recognize specific targets among the entire cohort of MEF2-regulated genes in the muscle genome. These findings provide opportunities to modulate the activity of MEF2 isoforms and their respective gene programs in skeletal muscle homeostasis and disease.

Indexed as

Evolution, MolecularAnimalsCell DifferentiationChlorocebus aethiopsCOS CellsDrosophilaGene Expression Regulation, DevelopmentalMammalsMEF2 Transcription FactorsMiceMuscle DevelopmentMuscle, SkeletalMyoblastsProtein IsoformsMEF2 Transcription FactorsProtein IsoformsDifferentiationMyogenesisRNA Interference (RNAi)Transcription FactorTranscriptomics

Identifiers

PMID25416778
PMCPMC4294490
OpenAlexW2004914475

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.