Evidence map›Paper›PMID 25144774›Full record

ArticlePLoS genetics2014

The MAP kinase p38 is part of Drosophila melanogaster's circadian clock.

Verena Dusik, Pingkalai R Senthilan, Benjamin Mentzel, Heiko Hartlieb, Corinna Wülbeck, Taishi Yoshii, Thomas Raabe, Charlotte Helfrich-Förster

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.3field-weighted citation impact, top 23% 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

12 citing papers in PubMed, 27 citations in OpenAlex.

  1. Post-Translational Modifications in Animal Circadian Clocks.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  2. The "yeast-drop" treatment protocol in theFrontiers in tuberculosis · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Functions of p38 MAP Kinases in the Central Nervous System.Frontiers in molecular neuroscience · 2020
    Review
  8. Review
  9. Article
  10. Frontiers in molecular neuroscience · 2018
    Article
  11. Molecular modulators of the circadian clock: lessons from flies and mice.Cellular and molecular life sciences : CMLS · 2017
    Review
  12. 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

8 authors at 3 institutions in 2 countries.

Verena DusikNeurobiology and Genetics, Biocenter, University of Würzburg, Würzburg, Germany.
Pingkalai R SenthilanNeurobiology and Genetics, Biocenter, University of Würzburg, Würzburg, Germany.
Benjamin MentzelInstitute of Medical Radiation and Cell Research, University of Würzburg, Würzburg, Germany.
Heiko HartliebNeurobiology and Genetics, Biocenter, University of Würzburg, Würzburg, Germany.
Corinna WülbeckInstitute of Zoology, University of Regensburg, Regensburg, Germany.
Taishi YoshiiGraduate School of Natural Science and Technology, Okayama University, Okayama, Japan.
Thomas RaabeInstitute of Medical Radiation and Cell Research, University of Würzburg, Würzburg, Germany.
Charlotte Helfrich-FörsterNeurobiology and Genetics, Biocenter, University of Würzburg, Würzburg, Germany.
University of Würzburg · DEOkayama University · JPUniversity of Regensburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

All organisms have to adapt to acute as well as to regularly occurring changes in the environment. To deal with these major challenges organisms evolved two fundamental mechanisms: the p38 mitogen-activated protein kinase (MAPK) pathway, a major stress pathway for signaling stressful events, and circadian clocks to prepare for the daily environmental changes. Both systems respond sensitively to light. Recent studies in vertebrates and fungi indicate that p38 is involved in light-signaling to the circadian clock providing an interesting link between stress-induced and regularly rhythmic adaptations of animals to the environment, but the molecular and cellular mechanisms remained largely unknown. Here, we demonstrate by immunocytochemical means that p38 is expressed in Drosophila melanogaster's clock neurons and that it is activated in a clock-dependent manner. Surprisingly, we found that p38 is most active under darkness and, besides its circadian activation, additionally gets inactivated by light. Moreover, locomotor activity recordings revealed that p38 is essential for a wild-type timing of evening activity and for maintaining ∼ 24 h behavioral rhythms under constant darkness: flies with reduced p38 activity in clock neurons, delayed evening activity and lengthened the period of their free-running rhythms. Furthermore, nuclear translocation of the clock protein Period was significantly delayed on the expression of a dominant-negative form of p38b in Drosophila's most important clock neurons. Western Blots revealed that p38 affects the phosphorylation degree of Period, what is likely the reason for its effects on nuclear entry of Period. In vitro kinase assays confirmed our Western Blot results and point to p38 as a potential "clock kinase" phosphorylating Period. Taken together, our findings indicate that the p38 MAP Kinase is an integral component of the core circadian clock of Drosophila in addition to playing a role in stress-input pathways.

Indexed as

AnimalsCircadian ClocksCircadian RhythmDarknessDrosophila melanogasterLightMotor ActivityNeuronsp38 Mitogen-Activated Protein KinasesPhosphorylationStress, Physiologicalp38 Mitogen-Activated Protein Kinases

Identifiers

PMID25144774
PMCPMC4140665
OpenAlexW2127992601

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.