Evidence map›Paper›PMID 23223572›Full record

ArticleMolecular biology of the cell2013

A dominant mutation in mec-7/β-tubulin affects axon development and regeneration in Caenorhabditis elegans neurons.

Leonie Kirszenblat, Brent Neumann, Sean Coakley, Massimo A Hilliard

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.1field-weighted citation impact, top 29% 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

26 citing papers in PubMed, 54 citations in OpenAlex.

  1. IndividualLife science alliance · 2026
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  11. CAMSAP3 maintains neuronal polarity through regulation of microtubule stability.Proceedings of the National Academy of Sciences of the United States of America · 2018
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  14. Phosphatidylserine save-me signals drive functional recovery of severed axons inProceedings of the National Academy of Sciences of the United States of America · 2017
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  15. Proceedings of the National Academy of Sciences of the United States of America · 2017
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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

4 authors at 1 institution in 1 country.

Leonie KirszenblatQueensland Brain Institute, The University of Queensland, Brisbane 4072, Australia.
Brent Neumann
Sean Coakley
Massimo A Hilliard
The University of Queensland · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microtubules have been known for decades to be basic elements of the cytoskeleton. They form long, dynamic, rope-like structures within the cell that are essential for mitosis, maintenance of cell shape, and intracellular transport. More recently, in vitro studies have implicated microtubules as signaling molecules that, through changes in their stability, have the potential to trigger growth of axons and dendrites in developing neurons. In this study, we show that specific mutations in the Caenorhabditis elegans mec-7/β-tubulin gene cause ectopic axon formation in mechanosensory neurons in vivo. In mec-7 mutants, the ALM mechanosensory neuron forms a long ectopic neurite that extends posteriorly, a phenotype that can be mimicked in wild-type worms with a microtubule-stabilizing drug (paclitaxel), and suppressed by mutations in unc-33/CRMP2 and the kinesin-related gene, vab-8. Our results also reveal that these ectopic neurites contain RAB-3, a marker for presynaptic loci, suggesting that they have axon-like properties. Interestingly, in contrast with the excessive axonal growth observed during development, mec-7 mutants are inhibited in axonal regrowth and remodeling following axonal injury. Together our results suggest that MEC-7/β-tubulin integrity is necessary for the correct number of neurites a neuron generates in vivo and for the capacity of an axon to regenerate.

Indexed as

AnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsColchicineGenes, DominantMitogen-Activated Protein KinasesMutationNerve Growth FactorsNerve RegenerationNeuritesNeuronsPhenotypePolymorphism, Single NucleotideProtein TransportSequence Analysis, DNASynapsesCaenorhabditis elegans ProteinsColchicineMec-7 protein, C elegansMitogen-Activated Protein KinasesNerve Growth FactorsTubulinTubulin Modulatorsunc-33 protein, C elegansvab-8 protein, C elegansWnt Proteins

Identifiers

PMID23223572
PMCPMC3564523
OpenAlexW2016982643

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.