Evidence map›Paper›PMID 16096739›Full record

ArticleJournal of molecular medicine (Berlin, Germany)2005

Atypical patterns of circadian clock gene expression in human peripheral blood mononuclear cells.

Michèle Teboul, Marie-Audrey Barrat-Petit, Xiao Mei Li, Bruno Claustrat, Jean-Louis Formento, Franck Delaunay, Francis Lévi, Gérard Milano

Abstract read
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In one paragraph

Article in Journal of molecular medicine (Berlin, Germany), 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

42 citing papers in PubMed, 103 citations in OpenAlex.

  1. Trial
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  7. Observational
  8. Disruption of central and peripheral circadian clocks and circadian controlled estrogen receptor rhythms in night shift nurses in working environments.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article
  9. Traumatic brain injury-induced disruption of the circadian clock.Journal of molecular medicine (Berlin, Germany) · 2024
    Article
  10. Article
  11. Article
  12. Cancers · 2019
    Article
  13. Article
  14. Article
  15. Systems Chronotherapeutics.Pharmacological reviews · 2017
    Review
  16. Article
  17. Article
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  19. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 5 institutions in 1 country.

Michèle TeboulUniversité de Nice-Sophia Antipolis, CNRS FRE 2721, Parc Valrose, 06108 Nice Cedex 2, France. teboulm@unice.fr
Marie-Audrey Barrat-Petit
Xiao Mei Li
Bruno Claustrat
Jean-Louis Formento
Franck Delaunay
Francis Lévi
Gérard Milano
Centre Antoine Lacassagne · FRCentre National de la Recherche Scientifique · FRHôpital Paul-Brousse · FRUniversité Côte d'Azur · FRUniversité Paris-Saclay · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Circadian ( approximately 24 h) rhythms in physiology and behaviour are observed in all mammals, including humans. These rhythms are generated by circadian clocks located in the hypothalamus and also in most peripheral tissues. Clock genes are essential components of circadian clocks, and mutations or polymorphisms within several of them have been associated with circadian disorders in humans. However, information about human clock gene expression has remained very limited. Peripheral blood mononuclear cells (PBMCs) represent an ideal material to investigate non-invasively the human clock at the molecular level. In the present study, we analysed the expression of three key clock genes, PER2, BMAL1 and REV-ERBalpha in PBMCs from ten healthy humans over a 24-h cycle. PER2 and BMAL1 were found to oscillate throughout the light-dark cycle in all subjects. Interestingly, despite normal melatonin and cortisol secretion patterns, two groups of subjects could be distinguished with significantly different mean PER2 and BMAL1 acrophases. BMAL1 oscillated with approximately the same phase as PER2, instead of being anti-phasic as anticipated from data previously obtained in other peripheral tissues. Furthermore, this unusual phase relationship of PER2 and BMAL1 in human PBMCs was associated with a constant expression of REV-ERBalpha, a crucial regulator of BMAL1, which is highly rhythmic in many other systems. These results reveal the existence of different chronotypes of clock gene expression patterns and suggest specific regulatory mechanisms in human PBMCs.

Indexed as

AdultARNTL Transcription FactorsBasic Helix-Loop-Helix ProteinsCircadian RhythmDNA-Binding ProteinsGene Expression RegulationHumansLeukocytes, MononuclearMaleNuclear ProteinsNuclear Receptor Subfamily 1, Group D, Member 1Period Circadian ProteinsReceptors, Cytoplasmic and NuclearTranscription FactorsARNTL Transcription FactorsBasic Helix-Loop-Helix ProteinsBMAL1 protein, humanDNA-Binding ProteinsNR1D1 protein, humanNuclear ProteinsNuclear Receptor Subfamily 1, Group D, Member 1PER2 protein, humanPeriod Circadian ProteinsReceptors, Cytoplasmic and NuclearTranscription Factors

Identifiers

PMID16096739
OpenAlexW2137414457

What OpenQuestion holds

Textmetadata
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.