Evidence map›Paper›PMID 23127194›Full record

ArticleThe European journal of neuroscience2013

Mitogen- and stress-activated protein kinase 1 modulates photic entrainment of the suprachiasmatic circadian clock.

Ruifeng Cao, Greg Q Butcher, Kate Karelina, J Simon Arthur, Karl Obrietan

Open access · greenAbstract read
In one paragraph

Article in The European journal of neuroscience, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.7field-weighted citation impact, top 35% 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

18 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
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  5. Review
  6. Article
  7. Haploinsufficiency of a Circadian Clock GeneInternational journal of molecular sciences · 2022
    Article
  8. Genome-wide circadian regulation: A unique system for computational biology.Computational and structural biotechnology journal · 2020
    Review
  9. Article
  10. Review
  11. 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 at 3 institutions in 2 countries.

Ruifeng CaoDepartment of Neuroscience, Ohio State University, Columbus, OH, USA.
Greg Q Butcher
Kate Karelina
J Simon Arthur
Karl Obrietan
The Ohio State University · USCentenary College of Louisiana · USMRC Protein Phosphorylation and Ubiquitylation Unit · GB

Funding

Ohio State Neuroscience Centr CoreP30NS045758 · NINDS · OHIO STATE UNIVERSITY · PI OBRIETAN, KARL H · 2004 to 2015
$7.7M
The ERK/MAPK Pathway and Circadian Clock EntrainmentR01MH062335 · NIMH · OHIO STATE UNIVERSITY · PI OBRIETAN, KARL H · 2002 to 2011
$2.9M
Activity-dependent microRNA expression and function in the mature nervous systemR01NS066345 · NINDS · OHIO STATE UNIVERSITY · PI IMPEY, SOREN, OBRIETAN, KARL H · 2010 to 2014
$1.9M
Mechanisms of hippocampal excitotoxic cell death and structural remodelingR01NS067409 · NINDS · OHIO STATE UNIVERSITY · PI OBRIETAN, KARL H · 2009 to 2010
$750k
Medical Research Council MC_U127081014NIMH NIH HHS MH62335NIMH NIH HHS R01 MH062335NINDS NIH HHS NS067409NINDS NIH HHS P30 NS045758NINDS NIH HHS R01 NS066345NINDS NIH HHS R01 NS067409
6 · The paper itself

Abstract

The master circadian clock in mammals, the suprachiasmatic nucleus (SCN), is under the entraining influence of the external light cycle. At a mechanistic level, intracellular signaling via the p42/44 mitogen-activated protein kinase pathway appears to play a central role in light-evoked clock entrainment; however, the precise downstream mechanisms by which this pathway influences clock timing are not known. Within this context, we have previously reported that light stimulates activation of the mitogen-activated protein kinase effector mitogen-stress-activated kinase 1 (MSK1) in the SCN. In this study, we utilised MSK1(-/-) mice to further investigate the potential role of MSK1 in circadian clock timing and entrainment. Locomotor activity analysis revealed that MSK1 null mice entrained to a 12 h light/dark cycle and exhibited circadian free-running rhythms in constant darkness. Interestingly, the free-running period in MSK1 null mice was significantly longer than in wild-type control animals, and MSK1 null mice exhibited a significantly greater variance in activity onset. Further, MSK1 null mice exhibited a significant reduction in the phase-delaying response to an early night light pulse (100 lux, 15 min), and, using an 8 h phase-advancing 'jet-lag' experimental paradigm, MSK1 knockout animals exhibited a significantly delayed rate of re-entrainment. At the molecular level, early night light-evoked cAMP response element-binding protein (CREB) phosphorylation, histone phosphorylation and Period1 gene expression were markedly attenuated in MSK1(-/-) animals relative to wild-type mice. Together, these data provide key new insights into the molecular mechanisms by which MSK1 affects the SCN clock.

Indexed as

AnimalsCircadian ClocksCircadian RhythmCyclic AMP Response Element-Binding ProteinHistonesJet Lag SyndromeMiceMice, KnockoutMotor ActivityPeriod Circadian ProteinsPhosphorylationPhotic StimulationPhotoperiodRibosomal Protein S6 Kinases, 90-kDaSuprachiasmatic NucleusTranscription, GeneticCreb1 protein, mouseCyclic AMP Response Element-Binding ProteinHistonesmitogen and stress-activated protein kinase 1Per1 protein, mousePeriod Circadian ProteinsRibosomal Protein S6 Kinases, 90-kDa

Identifiers

PMID23127194
PMCPMC3575747
OpenAlexW2159300019

What OpenQuestion holds

Textmetadata
LicenceTDM
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.