Evidence map›Paper›PMID 30462217›Full record

ArticleHuman molecular genetics2019

Dynamic transcriptomic analysis reveals suppression of PGC1α/ERRα drives perturbed myogenesis in facioscapulohumeral muscular dystrophy.

Christopher R S Banerji, Maryna Panamarova, Johanna Pruller, Nicolas Figeac, Husam Hebaishi, Efthymios Fidanis, Alka Saxena, Julian Contet, Sabrina Sacconi, Simone Severini and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Human molecular genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed, 1 pooled it
2.9field-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

48 citing papers in PubMed, 1 synthesis or guideline pooled it, 80 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Estrogen-Related Receptor Alpha Promotes Skeletal Muscle Regeneration and Mitigates Muscular Dystrophy.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  5. Review
  6. Article
  7. IncreasedInternational journal of molecular sciences · 2025
    Article
  8. Article
  9. Review
  10. Prenatal and progressive coenzyme QJournal of cachexia, sarcopenia and muscle · 2024
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Estrogen-related Receptor Signaling in Skeletal Muscle Fitness.International journal of sports medicine · 2023
    Article
  17. Article
  18. Article
  19. Review
  20. 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

11 authors at 4 institutions in 2 countries.

Christopher R S BanerjiRandall Centre for Cell and Molecular Biophysics, New Hunt's House, Guy's Campus, King's College London, London, UK.
Maryna PanamarovaRandall Centre for Cell and Molecular Biophysics, New Hunt's House, Guy's Campus, King's College London, London, UK.
Johanna PrullerRandall Centre for Cell and Molecular Biophysics, New Hunt's House, Guy's Campus, King's College London, London, UK.
Nicolas FigeacRandall Centre for Cell and Molecular Biophysics, New Hunt's House, Guy's Campus, King's College London, London, UK.
Husam HebaishiRandall Centre for Cell and Molecular Biophysics, New Hunt's House, Guy's Campus, King's College London, London, UK.
Efthymios FidanisGenomics Research Platform, Biomedical Research Centre at Guy's and St Thomas' Trust and Kings College London, Guy's Hospital, London, UK.
Alka SaxenaGenomics Research Platform, Biomedical Research Centre at Guy's and St Thomas' Trust and Kings College London, Guy's Hospital, London, UK.
Julian ContetInstitute for Research on Cancer and Aging of Nice, Faculty of Medicine, Université Côte d'Azur, Nice, Cedex, France.
Sabrina SacconiInstitute for Research on Cancer and Aging of Nice, Faculty of Medicine, Université Côte d'Azur, Nice, Cedex, France.
Simone SeveriniDepartment of Computer Science, University College London, London, UK.
Peter S ZammitRandall Centre for Cell and Molecular Biophysics, New Hunt's House, Guy's Campus, King's College London, London, UK.
King's College London · GBGuy's Hospital · GBUniversité Côte d'Azur · FRUniversity College London · GB

Funding

British Heart Foundation PG/13/1930059British Heart Foundation SP/08/004Medical Research Council MR/P023215/1Medical Research Council MR/S002472/1Wellcome TrustWellcome Trust WT - 203949/Z/16/Z
6 · The paper itself

Abstract

Facioscapulohumeral muscular dystrophy (FSHD) is a prevalent, incurable myopathy, linked to epigenetic derepression of D4Z4 repeats on chromosome 4q, leading to ectopic DUX4 expression. FSHD patient myoblasts have defective myogenic differentiation, forming smaller myotubes with reduced myosin content. However, molecular mechanisms driving such disrupted myogenesis in FSHD are poorly understood. We performed high-throughput morphological analysis describing FSHD and control myogenesis, revealing altered myogenic differentiation results in hypotrophic myotubes. Employing polynomial models and an empirical Bayes approach, we established eight critical time points during which human healthy and FSHD myogenesis differ. RNA-sequencing at these eight nodal time points in triplicate, provided temporal depth for a multivariate regression analysis, allowing assessment of interaction between progression of differentiation and FSHD disease status. Importantly, the unique size and structure of our data permitted identification of many novel FSHD pathomechanisms undetectable by previous approaches. For further analysis here, we selected pathways that control mitochondria: of interest considering known alterations in mitochondrial structure and function in FSHD muscle, and sensitivity of FSHD cells to oxidative stress. Notably, we identified suppression of mitochondrial biogenesis, in particular via peroxisome proliferator-activated receptor gamma coactivator 1-α (PGC1α), the cofactor and activator of oestrogen-related receptor α (ERRα). PGC1α knock-down caused hypotrophic myotubes to form from control myoblasts. Known ERRα agonists and safe food supplements biochanin A, daidzein or genistein, each rescued the hypotrophic FSHD myotube phenotype. Together our work describes transcriptomic changes in high resolution that occur during myogenesis in FSHD ex vivo, identifying suppression of the PGC1α-ERRα axis leading to perturbed myogenic differentiation, which can effectively be rescued by readily available food supplements.

Indexed as

AdultBayes TheoremCell DifferentiationCells, CulturedERRalpha Estrogen-Related ReceptorFemaleGene Expression ProfilingHigh-Throughput Screening AssaysHumansMaleMuscle DevelopmentMuscle Fibers, SkeletalMuscular Dystrophy, FacioscapulohumeralMyoblastsMyopathies, Structural, CongenitalPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaERRalpha Estrogen-Related ReceptorPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPPARGC1A protein, humanReceptors, Estrogen

Identifiers

PMID30462217
PMCPMC6452176
OpenAlexW2901813281

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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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.