Evidence map›Paper›PMID 26051896›Full record

ArticleCurrent biology : CB2015

Dynamic microtubules drive circuit rewiring in the absence of neurite remodeling.

Naina Kurup, Dong Yan, Alexandr Goncharov, Yishi Jin

Open access · bronzeAbstract read
In one paragraph

Article in Current biology : CB, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
4.4field-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

38 citing papers in PubMed, 54 citations in OpenAlex.

  1. Article
  2. eNeuro · 2026
    Article
  3. Kinesins inOpen biology · 2025
    Review
  4. Article
  5. AnalysisbioRxiv : the preprint server for biology · 2025
    Article
  6. Imaging microtubule dynamics: A new frontier in biomarker development for neurodegenerative diseases.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Review
  7. A tubulin-MAPKKK pathway engages tubulin isotype interaction for neuroprotection.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. The Expression and Function of Tubulin Isotypes inFrontiers in cell and developmental biology · 2022
    Review
  13. Article
  14. Review
  15. Microtubule control of functional architecture in neurons.Current opinion in neurobiology · 2019
    Review
  16. Review
  17. Review
  18. Article
  19. Article
  20. Review
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.

Naina KurupNeurobiology Section, Division of Biological Sciences, University of California, San Diego, La Jolla, CA 92093, USA.
Dong YanNeurobiology Section, Division of Biological Sciences, University of California, San Diego, La Jolla, CA 92093, USA.
Alexandr GoncharovHoward Hughes Medical Institute, University of California, San Diego, La Jolla, CA 92093, USA.
Yishi JinNeurobiology Section, Division of Biological Sciences, University of California, San Diego, La Jolla, CA 92093, USA; Howard Hughes Medical Institute, University of California, San Diego, La Jolla, CA 92093, USA; Department of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, CA 92093, USA. Electronic address: yijin@ucsd.edu.
University of California, San Diego · US

Funding

GABAERGIC NEURON DIFFERENTIATION IN C ELEGANSR01NS035546 · NINDS · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI JIN, YISHI · 1996 to 2016
$5.3M
Mechanisms of neural circuit formation in C. elegansR01NS094171 · NINDS · DUKE UNIVERSITY · PI YAN, DONG · 2015 to 2019
$1.5M
Regulation of the DLK-1 pathway in axon regenerationR00NS076646 · NINDS · DUKE UNIVERSITY · PI YAN, DONG · 2014 to 2016
$732k
Regulation of the DLK-1 pathway in axon regenerationK99NS076646 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI YAN, DONG · 2011 to 2012
$171k
Howard Hughes Medical InstituteNINDS NIH HHS K99 NS076646NINDS NIH HHS R00 NS076646NINDS NIH HHS R01 NS035546NINDS NIH HHS R01 NS094171
6 · The paper itself

Abstract

A striking neuronal connectivity change in C. elegans involves the coordinated elimination of existing synapses and formation of synapses at new locations, without altering neuronal morphology. Here, we investigate the tripartite interaction between dynamic microtubules (MTs), kinesin-1, and vesicular cargo during this synapse remodeling. We find that a reduction in the dynamic MT population in motor neuron axons, resulting from genetic interaction between loss of function in the conserved MAPKKK dlk-1 and an α-tubulin mutation, specifically blocks synapse remodeling. Using live imaging and pharmacological modulation of the MT cytoskeleton, we show that dynamic MTs are increased at the onset of remodeling and are critical for new synapse formation. DLK-1 acts during synapse remodeling, and its function involves MT catastrophe factors including kinesin-13/KLP-7 and spastin/SPAS-1. Through a forward genetic screen, we identify gain-of-function mutations in kinesin-1 that can compensate for reduced dynamic MTs to promote synaptic vesicle transport during remodeling. Our data provide in vivo evidence supporting the requirement of dynamic MTs for kinesin-1-dependent axonal transport and shed light on the role of the MT cytoskeleton in facilitating neural circuit plasticity.

Indexed as

AnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsMAP Kinase Kinase KinasesMicrotubulesMutationNeuritesNeuronal PlasticitySynapsesCaenorhabditis elegans ProteinsDLK-1 protein, C elegansMAP Kinase Kinase Kinases

Identifiers

PMID26051896
PMCPMC4470761
OpenAlexW1846293222

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.