Evidence map›Paper›PMID 24912679›Full record

ArticleMolecular and cellular biology2014

Transcriptional network analysis in muscle reveals AP-1 as a partner of PGC-1α in the regulation of the hypoxic gene program.

Mario Baresic, Silvia Salatino, Barbara Kupr, Erik van Nimwegen, Christoph Handschin

Abstract read
In one paragraph

Article in Molecular and cellular biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
–field-weighted citation impact
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

26 citing papers in PubMed.

  1. Article
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  4. Article
  5. Review
  6. Impaired age-associated mitochondrial translation is mitigated by exercise and PGC-1α.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  7. Review
  8. RNA-bound PGC-1α controls gene expression in liquid-like nuclear condensates.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  9. Review
  10. Article
  11. Review
  12. Mitochondrial regulator PGC-1a-Modulating the modulator.Current opinion in endocrine and metabolic research · 2019
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
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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

5 authors.

Mario BaresicFocal Area Growth and Development, Biozentrum, University of Basel, Basel, Switzerland.
Silvia SalatinoFocal Area Growth and Development, Biozentrum, University of Basel, Basel, Switzerland Focal Area Computational and Systems Biology, Biozentrum, University of Basel, Basel, Switzerland Swiss Institute of Bioinformatics, Basel, Switzerland.
Barbara KuprFocal Area Growth and Development, Biozentrum, University of Basel, Basel, Switzerland.
Erik van NimwegenFocal Area Computational and Systems Biology, Biozentrum, University of Basel, Basel, Switzerland Swiss Institute of Bioinformatics, Basel, Switzerland erik.vannimwegen@unibas.ch christoph.handschin@unibas.ch.
Christoph HandschinFocal Area Growth and Development, Biozentrum, University of Basel, Basel, Switzerland erik.vannimwegen@unibas.ch christoph.handschin@unibas.ch.

Funding

European Research Council 616830
6 · The paper itself

Abstract

Skeletal muscle tissue shows an extraordinary cellular plasticity, but the underlying molecular mechanisms are still poorly understood. Here, we use a combination of experimental and computational approaches to unravel the complex transcriptional network of muscle cell plasticity centered on the peroxisome proliferator-activated receptor γ coactivator 1α (PGC-1α), a regulatory nexus in endurance training adaptation. By integrating data on genome-wide binding of PGC-1α and gene expression upon PGC-1α overexpression with comprehensive computational prediction of transcription factor binding sites (TFBSs), we uncover a hitherto-underestimated number of transcription factor partners involved in mediating PGC-1α action. In particular, principal component analysis of TFBSs at PGC-1α binding regions predicts that, besides the well-known role of the estrogen-related receptor α (ERRα), the activator protein 1 complex (AP-1) plays a major role in regulating the PGC-1α-controlled gene program of the hypoxia response. Our findings thus reveal the complex transcriptional network of muscle cell plasticity controlled by PGC-1α.

Indexed as

Gene Regulatory NetworksAnimalsBinding SitesCell HypoxiaCell LineDNA-Binding ProteinsERRalpha Estrogen-Related ReceptorGene Expression RegulationMiceMuscle Fibers, SkeletalPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPPAR gammaPrincipal Component AnalysisReceptors, EstrogenRNA InterferenceTranscription Factor AP-1DNA-Binding ProteinsERRalpha Estrogen-Related ReceptorPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaPPAR gammaPpargc1a protein, mouseReceptors, EstrogenTranscription Factor AP-1Transcription Factors

Identifiers

PMID24912679
PMCPMC4135604

What OpenQuestion holds

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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.