Evidence map›Paper›PMID 21731503›Full record

ArticlePLoS genetics2011

Genomic convergence among ERRα, PROX1, and BMAL1 in the control of metabolic clock outputs.

Catherine R Dufour, Marie-Pier Levasseur, Nguyen Hoai Huong Pham, Lillian J Eichner, Brian J Wilson, Alexis Charest-Marcotte, David Duguay, Jean-François Poirier-Héon, Nicolas Cermakian, Vincent Giguère

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
4.5field-weighted citation impact, top 4% 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

63 citing papers in PubMed, 101 citations in OpenAlex.

  1. Article
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  3. Circadian clock and cancer.Military Medical Research · 2026
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  12. Transcriptional control of energy metabolism by nuclear receptors.Nature reviews. Molecular cell biology · 2022
    Review
  13. Article
  14. Article
  15. Nuclear Receptors and Clock Components in Cardiovascular Diseases.International journal of molecular sciences · 2021
    Review
  16. Article
  17. Article
  18. Review
  19. Review
  20. Review

3 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

10 authors at 3 institutions in 1 country.

Catherine R DufourGoodman Cancer Research Centre, Montréal, Canada.
Marie-Pier Levasseur
Nguyen Hoai Huong Pham
Lillian J Eichner
Brian J Wilson
Alexis Charest-Marcotte
David Duguay
Jean-François Poirier-Héon
Nicolas Cermakian
Vincent Giguère
Occupational Cancer Research Centre · CAMcGill University · CADouglas Mental Health University Institute · CA

Funding

Canadian Institutes of Health Research MOP-77763Canadian Institutes of Health Research MOP-84227
6 · The paper itself

Abstract

Metabolic homeostasis and circadian rhythms are closely intertwined biological processes. Nuclear receptors, as sensors of hormonal and nutrient status, are actively implicated in maintaining this physiological relationship. Although the orphan nuclear receptor estrogen-related receptor α (ERRα, NR3B1) plays a central role in the control of energy metabolism and its expression is known to be cyclic in the liver, its role in temporal control of metabolic networks is unknown. Here we report that ERRα directly regulates all major components of the molecular clock. ERRα-null mice also display deregulated locomotor activity rhythms and circadian period lengths under free-running conditions, as well as altered circulating diurnal bile acid and lipid profiles. In addition, the ERRα-null mice exhibit time-dependent hypoglycemia and hypoinsulinemia, suggesting a role for ERRα in modulating insulin sensitivity and glucose handling during the 24-hour light/dark cycle. We also provide evidence that the newly identified ERRα corepressor PROX1 is implicated in rhythmic control of metabolic outputs. To help uncover the molecular basis of these phenotypes, we performed genome-wide location analyses of binding events by ERRα, PROX1, and BMAL1, an integral component of the molecular clock. These studies revealed the existence of transcriptional regulatory loops among ERRα, PROX1, and BMAL1, as well as extensive overlaps in their target genes, implicating these three factors in the control of clock and metabolic gene networks in the liver. Genomic convergence of ERRα, PROX1, and BMAL1 transcriptional activity thus identified a novel node in the molecular circuitry controlling the daily timing of metabolic processes.

Indexed as

AnimalsARNTL Transcription FactorsBile Acids and SaltsBlood GlucoseBlotting, WesternChlorocebus aethiopsCholesterolCircadian RhythmCLOCK ProteinsCOS CellsERRalpha Estrogen-Related ReceptorGene Expression ProfilingGene Expression RegulationGluconeogenesisGlycolysisHep G2 CellsARNTL Transcription FactorsBile Acids and SaltsBlood GlucoseBmal1 protein, mouseCholesterolClock protein, mouseCLOCK ProteinsERRalpha Estrogen-Related ReceptorHomeodomain ProteinsInsulinProspero-Related Homeobox 1 ProteinReceptors, EstrogenTriglyceridesTumor Suppressor Proteins

Identifiers

PMID21731503
PMCPMC3121748
OpenAlexW2070543234

What OpenQuestion holds

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LicenceCC BY
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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.