Evidence map›Paper›PMID 27411367›Full record

ArticleJournal of cell science2016

The microtubule-severing protein fidgetin acts after dendrite injury to promote their degeneration.

Juan Tao, Chengye Feng, Melissa M Rolls

Open access · greenAbstract read
In one paragraph

Article in Journal of cell science, 2016. 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
2.3field-weighted citation impact, top 14% 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, 39 citations in OpenAlex.

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  16. Conserved Tao Kinase Activity Regulates Dendritic Arborization, Cytoskeletal Dynamics, and Sensory Function inThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  17. The microtubule regulatorGenes & development · 2020
    Article
  18. Review
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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

3 authors at 1 institution in 1 country.

Juan TaoDepartment of Biochemistry and Molecular Biology and The Huck Institutes of the Life Sciences, The Pennsylvania State University, University Park, PA 16802, USA.
Chengye FengDepartment of Biochemistry and Molecular Biology and The Huck Institutes of the Life Sciences, The Pennsylvania State University, University Park, PA 16802, USA.
Melissa M RollsDepartment of Biochemistry and Molecular Biology and The Huck Institutes of the Life Sciences, The Pennsylvania State University, University Park, PA 16802, USA mur22@psu.edu.ORCID 0000-0002-5021-4360
Pennsylvania State University · US

Funding

Using Drosophila Neurons to Identify Mechanisms that Control Microtubule PolarityR01GM085115 · NIGMS · PENNSYLVANIA STATE UNIVERSITY, THE · PI Melissa Rolls · 2010 to 2026
$5.1M
NIGMS NIH HHS R01 GM085115
6 · The paper itself

Abstract

After being severed from the cell body, axons initiate an active degeneration program known as Wallerian degeneration. Although dendrites also seem to have an active injury-induced degeneration program, no endogenous regulators of this process are known. Because microtubule disassembly has been proposed to play a role in both pruning and injury-induced degeneration, we used a Drosophila model to identify microtubule regulators involved in dendrite degeneration. We found that, when levels of fidgetin were reduced using mutant or RNA interference (RNAi) strategies, dendrite degeneration was delayed, but axon degeneration and dendrite pruning proceeded with normal timing. We explored two possible ways in which fidgetin could promote dendrite degeneration: (1) by acting constitutively to moderate microtubule stability in dendrites, or (2) by acting specifically after injury to disassemble microtubules. When comparing microtubule dynamics and stability in uninjured neurons with and without fidgetin, we could not find evidence that fidgetin regulated microtubule stability constitutively. However, we identified a fidgetin-dependent increase in microtubule dynamics in severed dendrites. We conclude that fidgetin acts after injury to promote disassembly of microtubules in dendrites severed from the cell body.

Indexed as

AcetylationAnimalsATPases Associated with Diverse Cellular ActivitiesAxonsDendritesDrosophila melanogasterDrosophila ProteinsMicrotubule-Associated ProteinsMicrotubulesModels, BiologicalNerve DegenerationNuclear ProteinsRNA InterferenceATPases Associated with Diverse Cellular ActivitiesDrosophila ProteinsFign protein, DrosophilaMicrotubule-Associated ProteinsNuclear ProteinsDendrite degenerationDendrite pruningMicrotubule severingWallerian degeneration

Identifiers

PMID27411367
PMCPMC5047702
OpenAlexW2467804091

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.