Evidence map›Paper›PMID 29383758›Full record

ArticleThe European journal of neuroscience2018

Circadian expression and functional characterization of PEA-15 within the mouse suprachiasmatic nucleus.

Kelin Wheaton, Sydney Aten, Lucas Sales Queiroz, Kyle Sullivan, John Oberdick, Kari R Hoyt, Karl Obrietan

Abstract read
In one paragraph

Article in The European journal of neuroscience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 49% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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

7 authors at 1 institution in 1 country.

Kelin WheatonDivision of Pharmacology, Ohio State University, Columbus, OH, 43210, USA.
Sydney AtenDepartment of Neuroscience, Ohio State University, Columbus, OH, 43210, USA.
Lucas Sales QueirozDivision of Pharmacology, Ohio State University, Columbus, OH, 43210, USA.
Kyle SullivanDepartment of Neuroscience, Ohio State University, Columbus, OH, 43210, USA.
John OberdickDepartment of Neuroscience, Ohio State University, Columbus, OH, 43210, USA.
Kari R HoytDivision of Pharmacology, Ohio State University, Columbus, OH, 43210, USA.
Karl ObrietanDepartment of Neuroscience, Ohio State University, Columbus, OH, 43210, USA.ORCID 0000-0002-7525-7121
The Ohio State University · US

Funding

Hippocampal Cellular RhythmsR01MH103361 · NIMH · OHIO STATE UNIVERSITY · PI OBRIETAN, KARL H · 2014 to 2018
$2.0M
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
MSK, RSK and the regulation of excitotoxic cell death and structural plasticityR01NS091302 · NINDS · OHIO STATE UNIVERSITY · PI OBRIETAN, KARL H · 2015 to 2018
$1.3M
NIMH NIH HHS R01 MH103361NINDS NIH HHS R01 NS066345NINDS NIH HHS R01 NS091302
6 · The paper itself

Abstract

The circadian timing system influences the functional properties of most, if not all, physiological processes. Central to the mammalian timing system is the suprachiasmatic nucleus (SCN) of the hypothalamus. The SCN functions as a 'master clock' that sets the phasing of ancillary circadian oscillator populations found throughout the body. Further, via an entraining input from the retina, the SCN ensures that the clock oscillators are synchronized to the daily light/dark cycle. A critical component of the SCN timing and entrainment systems is the p44/42 mitogen-activated protein kinase (ERK/MAPK) pathway. Here, we examined the expression and function of phosphoprotein-enriched in astrocytes (PEA-15), an ERK scaffold protein that serves as a key regulator of MAPK signaling. A combination of immunolabeling and Western blotting approaches revealed high levels of PEA-15 within the SCN. PEA-15 expression was enriched in distinct subpopulations of SCN neurons, including arginine vasopressin (AVP)-positive neurons of the SCN shell region. Further, expression profiling detected a significant circadian oscillation in PEA-15 expression within the SCN. Brief photic stimulation during the early subjective night led to a significant increase in PEA-15 phosphorylation, an event that can trigger ERK/PEA-15 dissociation. Consistent with this, co-immunoprecipitation assays revealed that PEA-15 is directly bound to ERK in the SCN and that photic stimulation leads to their dissociation. Finally, we show that PEA-15 regulates ERK/MAPK-dependent activation of the core clock gene period1. Together, these data raise the prospect that PEA-15 functions as a key regulator of the SCN timing system.

Indexed as

Circadian RhythmAnimalsApoptosis Regulatory ProteinsArginine VasopressinExtracellular Signal-Regulated MAP KinasesFemaleMaleMicePeriod Circadian ProteinsPhosphoproteinsPhosphorylationPhotic StimulationPhotoperiodSuprachiasmatic NucleusApoptosis Regulatory ProteinsArginine VasopressinExtracellular Signal-Regulated MAP KinasesPea15 protein, mousePer1 protein, mousePeriod Circadian ProteinsPhosphoproteinsC57Bl/6circadianERKPEA-15suprachiasmatic nucleus

Identifiers

PMID29383758
PMCPMC5880735
OpenAlexW2793668411

What OpenQuestion holds

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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.