Evidence map›Paper›PMID 25186760›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2014

14-3-3ε and ζ regulate neurogenesis and differentiation of neuronal progenitor cells in the developing brain.

Kazuhito Toyo-oka, Tomoka Wachi, Robert F Hunt, Scott C Baraban, Shinichiro Taya, Hayley Ramshaw, Kozo Kaibuchi, Quenten P Schwarz, Angel F Lopez, Anthony Wynshaw-Boris

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed, 1 pooled it
4.1field-weighted citation impact, top 5% 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

74 citing papers in PubMed, 1 synthesis or guideline pooled it, 128 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Understanding the Molecular Basis of Miller-Dieker Syndrome.International journal of molecular sciences · 2025
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  12. Regulation of Ras Signaling by S-Nitrosylation.Antioxidants (Basel, Switzerland) · 2023
    Review
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14 more citing papers are in PubMed but not listed here.

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

10 authors at 6 institutions in 3 countries.

Kazuhito Toyo-okaDepartment of Pediatrics and Institute for Human Genetics, University of California, San Francisco School of Medicine, San Francisco, California 94143, Department of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, Pennsylvania 19129, ajw168@case.edu ktoyooka@drexelmed.edu.
Tomoka WachiDepartment of Pediatrics and Institute for Human Genetics, University of California, San Francisco School of Medicine, San Francisco, California 94143, Department of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, Pennsylvania 19129.
Robert F HuntEpilepsy Research Laboratory, Department of Neurological Surgery, University of California, San Francisco, San Francisco, California 94143.
Scott C BarabanEpilepsy Research Laboratory, Department of Neurological Surgery, University of California, San Francisco, San Francisco, California 94143.
Shinichiro TayaDepartment of Cell Pharmacology, Nagoya University Graduate School of Medicine, Nagoya, Aichi 466-8550, Japan.
Hayley RamshawDepartment of Human Immunology, Centre for Cancer Biology, South Australia Pathology, Adelaide, South Australia, Australia, and.
Kozo KaibuchiDepartment of Cell Pharmacology, Nagoya University Graduate School of Medicine, Nagoya, Aichi 466-8550, Japan.
Quenten P SchwarzDepartment of Human Immunology, Centre for Cancer Biology, South Australia Pathology, Adelaide, South Australia, Australia, and.
Angel F LopezDepartment of Human Immunology, Centre for Cancer Biology, South Australia Pathology, Adelaide, South Australia, Australia, and.
Anthony Wynshaw-BorisDepartment of Pediatrics and Institute for Human Genetics, University of California, San Francisco School of Medicine, San Francisco, California 94143, Department of Genetics and Genome Sciences, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106 ajw168@case.edu ktoyooka@drexelmed.edu.
South Australia Pathology · AUDrexel University · USNagoya University · JPNeurological Surgery · USUniversity of California, San Francisco · USUniversity School · US

Funding

Epileptogenesis in the Malformed BrainR01NS040272 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BARABAN, SCOTT C · 2001 to 2013
$3.5M
Dishevelled-Mediated Control of Wnt/PCP PathwaysR01NS073159 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WYNSHAW-BORIS, ANTHONY J. · 2010 to 2014
$1.9M
Genetic Regulation of Neuronal MigrationR01HD047380 · NICHD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WYNSHAW-BORIS, ANTHONY J. · 2005 to 2009
$1.2M
NR2B-dependent synaptic plasticityR01NS041310 · NINDS · RUTGERS THE ST UNIV OF NJ NEW BRUNSWICK · PI PLUMMER, MARK R. · 2002 to 2006
$1.2M
Functional engraftment of stem cell-derived cortical interneuronsR00NS085046 · NINDS · UNIVERSITY OF CALIFORNIA-IRVINE · PI HUNT, ROBERT F · 2015 to 2017
$747k
Functional engraftment of stem cell-derived cortical interneuronsK99NS085046 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HUNT, ROBERT F · 2013 to 2014
$176k
NICHD NIH HHS HD047380NICHD NIH HHS R01 HD047380NINDS NIH HHS K99 NS085046NINDS NIH HHS NS040272NINDS NIH HHS NS041310NINDS NIH HHS NS073159NINDS NIH HHS NS085046NINDS NIH HHS R00 NS085046NINDS NIH HHS R01 NS040272NINDS NIH HHS R01 NS041310NINDS NIH HHS R01 NS073159Wellcome Trust
6 · The paper itself

Abstract

During brain development, neural progenitor cells proliferate and differentiate into neural precursors. These neural precursors migrate along the radial glial processes and localize at their final destination in the cortex. Numerous reports have revealed that 14-3-3 proteins are involved in many neuronal activities, although their functions in neurogenesis remain unclear. Here, using 14-3-3ε/ζ double knock-out mice, we found that 14-3-3 proteins are important for proliferation and differentiation of neural progenitor cells in the cortex, resulting in neuronal migration defects and seizures. 14-3-3 deficiency resulted in the increase of δ-catenin and the decrease of β-catenin and αN-catenin. 14-3-3 proteins regulated neuronal differentiation into neurons via direct interactions with phosphorylated δ-catenin to promote F-actin formation through a catenin/Rho GTPase/Limk1/cofilin signaling pathway. Conversely, neuronal migration defects seen in the double knock-out mice were restored by phosphomimic Ndel1 mutants, but not δ-catenin. Our findings provide new evidence that 14-3-3 proteins play important roles in neurogenesis and neuronal migration via the regulation of distinct signaling cascades.

Indexed as

Neurogenesis14-3-3 ProteinsActinsAnimalsCateninsCell MovementCell ProliferationCerebral CortexMiceMice, Inbred C57BLNeural Stem CellsNeuronsProtein Binding14-3-3 ProteinsActinsCateninsYwhae protein, mouseYwhaz protein, mouse14-3-3delta-cateninneurogenesisneuronal differentiationneuronal migration

Identifiers

PMID25186760
PMCPMC4152612
OpenAlexW2029450515

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.