Evidence map›Paper›PMID 26484536›Full record

ArticlePLoS genetics2015

Axon Regeneration Is Regulated by Ets-C/EBP Transcription Complexes Generated by Activation of the cAMP/Ca2+ Signaling Pathways.

Chun Li, Naoki Hisamoto, Kunihiro Matsumoto

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
1.6field-weighted citation impact, top 19% 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

28 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
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  3. CaMKIIβ-mediated Phosphorylation Enhances Protein Stability of Spastin to Promote Neurite Outgrowth.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
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  5. Unzipping the defense: a comprehensive review on bZIP transcription factors inFrontiers in cellular and infection microbiology · 2025
    Review
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  11. Review
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  13. Review
  14. Article
  15. The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  16. [Research progress on intrinsic signaling pathways in axon regeneration].Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2020
    Review
  17. Article
  18. The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  19. Functional Dissection ofFrontiers in cellular neuroscience · 2019
    Article
  20. 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

3 authors at 1 institution in 1 country.

Chun LiDivision of Biological Science, Graduate School of Science, Nagoya University, Chikusa-ku, Nagoya, Japan.
Naoki HisamotoDivision of Biological Science, Graduate School of Science, Nagoya University, Chikusa-ku, Nagoya, Japan.
Kunihiro MatsumotoDivision of Biological Science, Graduate School of Science, Nagoya University, Chikusa-ku, Nagoya, Japan.
Nagoya University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ability of specific neurons to regenerate their axons after injury is governed by cell-intrinsic regeneration pathways. In Caenorhabditis elegans, the JNK and p38 MAPK pathways are important for axon regeneration. Axonal injury induces expression of the svh-2 gene encoding a receptor tyrosine kinase, stimulation of which by the SVH-1 growth factor leads to activation of the JNK pathway. Here, we identify ETS-4 and CEBP-1, related to mammalian Ets and C/EBP, respectively, as transcriptional activators of svh-2 expression following axon injury. ETS-4 and CEBP-1 function downstream of the cAMP and Ca2+-p38 MAPK pathways, respectively. We show that PKA-dependent phosphorylation of ETS-4 promotes its complex formation with CEBP-1. Furthermore, activation of both cAMP and Ca2+ signaling is required for activation of svh-2 expression. Thus, the cAMP/Ca2+ signaling pathways cooperatively activate the JNK pathway, which then promotes axon regeneration.

Indexed as

AnimalsAxonsCaenorhabditis elegansCaenorhabditis elegans ProteinsCalcium SignalingCCAAT-Enhancer-Binding ProteinsCyclic AMPGene Expression Regulation, DevelopmentalIntercellular Signaling Peptides and ProteinsMAP Kinase Signaling SystemNeuronsp38 Mitogen-Activated Protein KinasesPhosphorylationRegenerationSignal TransductionTranscription FactorsCaenorhabditis elegans ProteinsCCAAT-Enhancer-Binding ProteinsCyclic AMPETS-4 protein, C elegansIntercellular Signaling Peptides and Proteinsp38 Mitogen-Activated Protein KinasesSVH-1 protein, C elegansTranscription Factors

Identifiers

PMID26484536
PMCPMC4618690
OpenAlexW1803436910

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.