Evidence map›Paper›PMID 25242327›Full record

ArticleCell reports2014

NFATc1 controls skeletal muscle fiber type and is a negative regulator of MyoD activity.

Melissa L Ehlers, Barbara Celona, Brian L Black

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed, 1 pooled it
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

54 citing papers in PubMed, 1 synthesis or guideline pooled it, 104 citations in OpenAlex.

  1. Pooled it
  2. Ets2 Is an Activity-Dependent Transcriptional Regulator of a Fast-Twitch Muscle Program.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
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  20. Developmental, physiologic and phylogenetic perspectives on the expression and regulation of myosin heavy chains in mammalian skeletal muscles.Journal of comparative physiology. B, Biochemical, systemic, and environmental physiology · 2023
    Review
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

3 authors at 1 institution in 1 country.

Melissa L EhlersCardiovascular Research Institute, University of California, San Francisco, CA 94158-2517, USA.
Barbara CelonaCardiovascular Research Institute, University of California, San Francisco, CA 94158-2517, USA.
Brian L BlackCardiovascular Research Institute, University of California, San Francisco, CA 94158-2517, USA; Department of Biochemistry and Biophysics, University of California, San Francisco, CA 94158-2517, USA. Electronic address: brian.black@ucsf.edu.
University of California, San Francisco · US

Funding

Transcriptional Networks During Cardiac DifferentiationP01HL089707 · NHLBI · J. DAVID GLADSTONE INSTITUTES · PI SRIVASTAVA, DEEPAK · 2008 to 2017
$20.4M
Regulation of cardiovascular transcriptionR01HL064658 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BLACK, BRIAN L · 2000 to 2019
$5.4M
Molecular and Genetic Regulation of Craniofacial DevelopmentR01DE019118 · NIDCR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BLACK, BRIAN L · 2009 to 2013
$1.9M
NHLBI NIH HHS HL064658NHLBI NIH HHS HL089707NHLBI NIH HHS P01 HL089707NHLBI NIH HHS R01 HL064658NIDCR NIH HHS DE019118NIDCR NIH HHS R01 DE019118
6 · The paper itself

Abstract

Skeletal muscle comprises a heterogeneous population of fibers with important physiological differences. Fast fibers are glycolytic and fatigue rapidly. Slow fibers utilize oxidative metabolism and are fatigue resistant. Muscle diseases such as sarcopenia and atrophy selectively affect fast fibers, but the molecular mechanisms regulating fiber type-specific gene expression remain incompletely understood. Here, we show that the transcription factor NFATc1 controls fiber type composition and is required for fast-to-slow fiber type switching in response to exercise in vivo. Moreover, MyoD is a crucial transcriptional effector of the fast fiber phenotype, and we show that NFATc1 inhibits MyoD-dependent fast fiber gene promoters by physically interacting with the N-terminal activation domain of MyoD and blocking recruitment of the essential transcriptional coactivator p300. These studies establish a molecular mechanism for fiber type switching through direct inhibition of MyoD to control the opposing roles of MyoD and NFATc1 in fast versus slow fiber phenotypes.

Indexed as

AnimalsFemaleMaleMEF2 Transcription FactorsMiceMice, KnockoutMuscle Fibers, SkeletalMutagenesisMyoD ProteinNFATC Transcription Factorsp300-CBP Transcription FactorsPhenotypePhysical Conditioning, AnimalPromoter Regions, GeneticProtein BindingProtein IsoformsMEF2 Transcription FactorsMyoD ProteinNFATC Transcription Factorsp300-CBP Transcription FactorsProtein Isoforms

Identifiers

PMID25242327
PMCPMC4180018
OpenAlexW2033561732

What OpenQuestion holds

Textmetadata
LicenceTDM
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.