Evidence map›Paper›PMID 23154418›Full record

ArticleDevelopment (Cambridge, England)2013

MEF2A regulates the Gtl2-Dio3 microRNA mega-cluster to modulate WNT signaling in skeletal muscle regeneration.

Christine M Snyder, Amanda L Rice, Nelsa L Estrella, Aaron Held, Susan C Kandarian, Francisco J Naya

Open access · greenAbstract read
In one paragraph

Article in Development (Cambridge, England), 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

73 citing papers in PubMed, 115 citations in OpenAlex.

  1. Article
  2. Article
  3. miR-433 targets BMP and Indian hedgehog signaling to coordinate murine postnatal growth plate dynamics.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2026
    Article
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  7. Article
  8. Article
  9. Article
  10. Article
  11. Effect of BovineGenes · 2023
    Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Non-coding RNA basis of muscle atrophy.Molecular therapy. Nucleic acids · 2021
    Review
  19. Review
  20. Article

13 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.

Christine M SnyderDepartment of Biology, Program in Cell and Molecular Biology, Boston University, Boston, MA 02215, USA.
Amanda L Rice
Nelsa L Estrella
Aaron Held
Susan C Kandarian
Francisco J Naya
Boston University · US

Funding

MEF2 Function in Cardiac Muscle DevelopmentR01HL073304 · NHLBI · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI NAYA, FRANCISCO J · 2003 to 2013
$3.3M
The Molecular Basis of Muscle Wasting in Cancer CachexiaR01AR060217 · NIAMS · BOSTON UNIVERSITY (CHARLES RIVER CAMPUS) · PI JACKMAN, ROBERT W, KANDARIAN, SUSAN · 2011 to 2015
$1.8M
NHLBI NIH HHS HL73304NHLBI NIH HHS R01 HL073304NIAMS NIH HHS R01 AR060217
6 · The paper itself

Abstract

Understanding the molecular mechanisms of skeletal muscle regeneration is crucial to exploiting this pathway for use in tissue repair. Our data demonstrate that the MEF2A transcription factor plays an essential role in skeletal muscle regeneration in adult mice. Injured Mef2a knockout mice display widespread necrosis and impaired myofiber formation. MEF2A controls this process through its direct regulation of the largest known mammalian microRNA (miRNA) cluster, the Gtl2-Dio3 locus. A subset of the Gtl2-Dio3 miRNAs represses secreted Frizzled-related proteins (sFRPs), inhibitors of WNT signaling. Consistent with these data, Gtl2-Dio3-encoded miRNAs are downregulated in regenerating Mef2a knockout muscle, resulting in upregulated sFRP expression and attenuated WNT activity. Furthermore, myogenic differentiation in Mef2a-deficient myoblasts is rescued by overexpression of miR-410 and miR-433, two miRNAs in the Gtl2-Dio3 locus that repress sFRP2, or by treatment with recombinant WNT3A and WNT5A. Thus, miRNA-mediated modulation of WNT signaling by MEF2A is a requisite step for proper muscle regeneration, and represents an attractive pathway for enhancing regeneration of diseased muscle.

Indexed as

AnimalsCarbocyaninesCell LineCells, CulturedChlorocebus aethiopsCOS CellsFrizzled ReceptorsGene Knockdown TechniquesHumansMEF2 Transcription FactorsMiceMice, KnockoutMicroRNAsMuscle, SkeletalMyogenic Regulatory FactorsRegeneration3,3'-dipropyloxadicarbocyanineCarbocyaninesFrizzled ReceptorsMef2a protein, mouseMEF2 Transcription FactorsMEG3 non-coding RNA, mouseMicroRNAsMyogenic Regulatory FactorsRNA, Long NoncodingWnt Proteins

Identifiers

PMID23154418
PMCPMC3513991
OpenAlexW2158992273

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.