Evidence map›Paper›PMID 27880909›Full record

ArticleCell reports2016

Nfix Induces a Switch in Sox6 Transcriptional Activity to Regulate MyHC-I Expression in Fetal Muscle.

Valentina Taglietti, Giovanni Maroli, Solei Cermenati, Stefania Monteverde, Andrea Ferrante, Giuliana Rossi, Giulio Cossu, Monica Beltrame, Graziella Messina

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

27 citing papers in PubMed, 39 citations in OpenAlex.

  1. Dynamic NFIX Promoter Usage Shapes Stem and Committed Myogenic States.International journal of molecular sciences · 2026
    Article
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  6. Regulatory Role ofInternational journal of molecular sciences · 2024
    Article
  7. Review
  8. 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
  9. Article
  10. International journal of molecular sciences · 2022
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  18. Article
  19. Reorganization of chromatin architecture during prenatal development of porcine skeletal muscle.DNA research : an international journal for rapid publication of reports on genes and genomes · 2021
    Article
  20. Inhibition of lncRNA MAAT Controls Multiple Types of Muscle Atrophy by cis- and trans-Regulatory Actions.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
    Article
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

9 authors at 2 institutions in 2 countries.

Valentina TagliettiDepartment of Biosciences, University of Milan, Milan 20133, Italy.
Giovanni MaroliDepartment of Biosciences, University of Milan, Milan 20133, Italy.
Solei CermenatiDepartment of Biosciences, University of Milan, Milan 20133, Italy.
Stefania MonteverdeDepartment of Biosciences, University of Milan, Milan 20133, Italy.
Andrea FerranteDepartment of Biosciences, University of Milan, Milan 20133, Italy.
Giuliana RossiDepartment of Biosciences, University of Milan, Milan 20133, Italy.
Giulio CossuDepartment of Biosciences, University of Milan, Milan 20133, Italy; Division of Cell Matrix Biology and Regenerative Medicine, University of Manchester, Oxford Road, M13 9PL Manchester, UK.
Monica BeltrameDepartment of Biosciences, University of Milan, Milan 20133, Italy.
Graziella MessinaDepartment of Biosciences, University of Milan, Milan 20133, Italy. Electronic address: graziella.messina@unimi.it.
University of Milan · ITUniversity of Manchester · GB

Funding

British Heart Foundation PG/14/1/30549
6 · The paper itself

Abstract

Sox6 belongs to the Sox gene family and plays a pivotal role in fiber type differentiation, suppressing transcription of slow-fiber-specific genes during fetal development. Here, we show that Sox6 plays opposite roles in MyHC-I regulation, acting as a positive and negative regulator of MyHC-I expression during embryonic and fetal myogenesis, respectively. During embryonic myogenesis, Sox6 positively regulates MyHC-I via transcriptional activation of Mef2C, whereas during fetal myogenesis, Sox6 requires and cooperates with the transcription factor Nfix in repressing MyHC-I expression. Mechanistically, Nfix is necessary for Sox6 binding to the MyHC-I promoter and thus for Sox6 repressive function, revealing a key role for Nfix in driving Sox6 activity. This feature is evolutionarily conserved, since the orthologs Nfixa and Sox6 contribute to repression of the slow-twitch phenotype in zebrafish embryos. These data demonstrate functional cooperation between Sox6 and Nfix in regulating MyHC-I expression during prenatal muscle development.

Indexed as

Transcription, GeneticAnimalsConserved SequenceEmbryo, NonmammalianEvolution, MolecularFetusGene Expression Regulation, DevelopmentalMEF2 Transcription FactorsMiceModels, BiologicalMuscle DevelopmentMuscle, SkeletalMyoblastsMyosin Heavy ChainsNFI Transcription FactorsPhenotypeMEF2 Transcription FactorsMyosin Heavy ChainsNFI Transcription Factorsnfixa protein, zebrafishNfix protein, mouseSOXD Transcription FactorsZebrafish ProteinsMyHC-ImyogenesisNfixSox6

Identifiers

PMID27880909
PMCPMC5149531
OpenAlexW2557223986

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.