Evidence map›Paper›PMID 19144847›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2009

Ribosomal s6 kinase cooperates with casein kinase 2 to modulate the Drosophila circadian molecular oscillator.

Bikem Akten, Michelle M Tangredi, Eike Jauch, Mary A Roberts, Fanny Ng, Thomas Raabe, F Rob Jackson

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
0.9field-weighted citation impact, top 31% 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

24 citing papers in PubMed, 29 citations in OpenAlex.

  1. Journal of biological rhythms · 2026
    Article
  2. Post-Translational Modifications in Animal Circadian Clocks.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
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  9. Frontiers in molecular neuroscience · 2018
    Article
  10. Article
  11. Molecular modulators of the circadian clock: lessons from flies and mice.Cellular and molecular life sciences : CMLS · 2017
    Review
  12. Review
  13. Article
  14. 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

7 authors at 2 institutions in 2 countries.

Bikem AktenDepartment of Neuroscience, Tufts Center for Neuroscience Research, Sackler School of Graduate Biomedical Sciences, Tufts University School of Medicine, Boston, Massachusetts 02111, USA.
Michelle M Tangredi
Eike Jauch
Mary A Roberts
Fanny Ng
Thomas Raabe
F Rob Jackson
Tufts University · USUniversity of Würzburg · DE

Funding

TUSM/T-NEMC CENTER FOR NEUROSCIENCE RESEARCH - Imaging CoreP30NS047243 · NINDS · TUFTS UNIVERSITY BOSTON · PI JACKSON, F ROB · 2003 to 2017
$10.0M
Role of Andante/CKIIB in the Drosophila Circadian ClockR01NS045817 · NINDS · TUFTS UNIVERSITY BOSTON · PI JACKSON, F. ROB · 2003 to 2007
$1.5M
NINDS NIH HHS P30 NS047243NINDS NIH HHS R01 NS045817NINDS NIH HHS R01 NS45817
6 · The paper itself

Abstract

There is a universal requirement for post-translational regulatory mechanisms in circadian clock systems. Previous work in Drosophila has identified several kinases, phosphatases, and an E3 ligase that are critical for determining the nuclear translocation and/or stability of clock proteins. The present study evaluated the function of p90 ribosomal S6 kinase (RSK) in the Drosophila circadian system. In mammals, RSK1 is a light- and clock-regulated kinase known to be activated by the mitogen-activated protein kinase pathway, but there is no direct evidence that it functions as a component of the circadian system. Here, we show that Drosophila S6KII RNA displays rhythms in abundance, indicative of circadian control. Importantly, an S6KII null mutant exhibits a short-period circadian phenotype that can be rescued by expression of the wild-type gene in clock neurons, indicating a role for S6KII in the molecular oscillator. Peak PER clock protein expression is elevated in the mutant, indicative of enhanced stability, whereas per mRNA level is decreased, consistent with enhanced feedback repression. Gene reporter assays show that decreased S6KII is associated with increased PER repression. Surprisingly, we demonstrate a physical interaction between S6KII and the casein kinase 2 regulatory subunit (CK2beta), suggesting a functional relationship between the two kinases. In support of such a relationship, there are genetic interactions between S6KII and CK2 mutations, in vivo, which indicate that CK2 activity is required for S6KII action. We propose that the two kinases cooperate within clock neurons to fine-tune circadian period, improving the precision of the clock mechanism.

Indexed as

PeriodicityAnimalsAnimals, Genetically ModifiedCasein Kinase IICell Line, TransformedCircadian RhythmDrosophilaDrosophila ProteinsGene Expression RegulationHumansMotor ActivityMutationNuclear ProteinsPeriod Circadian ProteinsRibosomal Protein S6 KinasesRNA InterferenceCasein Kinase IIDrosophila ProteinsNuclear ProteinsPeriod Circadian ProteinsPER protein, DrosophilaRibosomal Protein S6 KinasesRNA, Messenger

Identifiers

PMID19144847
PMCPMC2775553
OpenAlexW2158207742

What OpenQuestion holds

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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.