Evidence map›Paper›PMID 27881663›Full record

ArticleMolecular biology of the cell2017

Periodic actin structures in neuronal axons are required to maintain microtubules.

Yue Qu, Ines Hahn, Stephen E D Webb, Simon P Pearce, Andreas Prokop

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
7.4field-weighted citation impact, top 2% 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

77 citing papers in PubMed, 125 citations in OpenAlex.

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  8. GSK-3β coordinates axonal microtubule organization through Shot and Tau.Proceedings of the National Academy of Sciences of the United States of America · 2026
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17 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

5 authors at 2 institutions in 1 country.

Yue QuFaculty of Biology, Medicine and Health, University of Manchester, Manchester M13 9PT, United Kingdom.
Ines HahnFaculty of Biology, Medicine and Health, University of Manchester, Manchester M13 9PT, United Kingdom.
Stephen E D WebbRutherford Appleton Laboratory, Science and Technology Facilities Council, Didcot OX11 0QX, United Kingdom.
Simon P PearceFaculty of Biology, Medicine and Health, University of Manchester, Manchester M13 9PT, United Kingdom.
Andreas ProkopFaculty of Biology, Medicine and Health, University of Manchester, Manchester M13 9PT, United Kingdom Andreas.Prokop@manchester.ac.uk.
University of Manchester · GBRutherford Appleton Laboratory · GB

Funding

Resource Component: Acquisition, maintenance and distribution of Drosophila stocksP40OD018537 · OD · TRUSTEES OF INDIANA UNIVERSITY · PI Annette L. Parks · 2014 to 2026
$13.5M
Biotechnology and Biological Sciences Research Council BB/L000717/1Biotechnology and Biological Sciences Research Council BB/L014327/1Biotechnology and Biological Sciences Research Council BB/M007553/1Medical Research Council MC_EX_MR/K015591/1Medical Research Council MR/K015591/1NIH HHS P40 OD018537Wellcome Trust 087742/Z/08/Z
6 · The paper itself

Abstract

Axons are cable-like neuronal processes wiring the nervous system. They contain parallel bundles of microtubules as structural backbones, surrounded by regularly spaced actin rings termed the periodic membrane skeleton (PMS). Despite being an evolutionarily conserved, ubiquitous, highly ordered feature of axons, the function of PMS is unknown. Here we studied PMS abundance, organization, and function, combining versatile Drosophila genetics with superresolution microscopy and various functional readouts. Analyses with 11 actin regulators and three actin-targeting drugs suggest that PMS contains short actin filaments that are depolymerization resistant and sensitive to spectrin, adducin, and nucleator deficiency, consistent with microscopy-derived models proposing PMS as specialized cortical actin. Upon actin removal, we observed gaps in microtubule bundles, reduced microtubule polymerization, and reduced axon numbers, suggesting a role of PMS in microtubule organization. These effects become strongly enhanced when carried out in neurons lacking the microtubule-stabilizing protein Short stop (Shot). Combining the aforementioned actin manipulations with Shot deficiency revealed a close correlation between PMS abundance and microtubule regulation, consistent with a model in which PMS-dependent microtubule polymerization contributes to their maintenance in axons. We discuss potential implications of this novel PMS function along axon shafts for axon maintenance and regeneration.

Indexed as

Actin CytoskeletonActinsAnimalsAxonsCells, CulturedCytoskeletonDrosophilaDrosophila ProteinsMicrofilament ProteinsMicrotubule-Associated ProteinsMicrotubulesNeuronsTubulinActinsDrosophila ProteinsMicrofilament ProteinsMicrotubule-Associated ProteinsTubulin

Identifiers

PMID27881663
PMCPMC5231898
OpenAlexW2953017850

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.