Evidence map›Paper›PMID 40627464›Full record

ArticleThe Journal of cell biology2025

Myosin 15 participates in assembly and remodeling of the presynapse.

Astrid G Petzoldt, Marc J F Escher, Oriane Turrel, Niclas Gimber, Ina M Schedina, Sophie Walter, Torsten W B Götz, Marta Maglione, David Toppe, Tanja Matkovic-Rachid and 6 more

Abstract read
In one paragraph

Article in The Journal of cell biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Neuronal Actin Remodeling and Its Role in Higher Nervous Activity.International journal of molecular sciences · 2025
    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

16 authors.

Astrid G PetzoldtInstitute of Biology, Freie Universität Berlin , Berlin, Germany.ORCID 0000-0002-4059-7142
Marc J F EscherInstitute of Biology, Freie Universität Berlin , Berlin, Germany.ORCID 0000-0001-8952-0843
Oriane TurrelInstitute of Biology, Freie Universität Berlin , Berlin, Germany.ORCID 0000-0003-2174-7659
Niclas GimberAdvanced Medical Bioimaging Core Facility, Charité-Universitätsmedizin , Berlin, Germany.ORCID 0000-0001-9456-3063
Ina M SchedinaInstitute of Biology, Freie Universität Berlin , Berlin, Germany.ORCID 0009-0002-3381-1347
Sophie WalterInstitute of Biology, Freie Universität Berlin , Berlin, Germany.ORCID 0009-0001-2147-9925
Torsten W B GötzInstitute of Biology, Freie Universität Berlin , Berlin, Germany.ORCID 0000-0002-5894-1474
Marta MaglioneInstitute of Biology, Freie Universität Berlin , Berlin, Germany.ORCID 0000-0001-9052-9271
David ToppeInstitute of Biology, Freie Universität Berlin , Berlin, Germany.ORCID 0009-0009-2967-1442
Tanja Matkovic-RachidInstitute of Biology, Freie Universität Berlin , Berlin, Germany.ORCID 0009-0003-2953-6191
Alexander NeumannInstitute of Biology, Freie Universität Berlin , Berlin, Germany.ORCID 0009-0009-3820-2613
Janine LützkendorfInstitute of Biology, Freie Universität Berlin , Berlin, Germany.ORCID 0000-0001-5051-6281
Jan SchmoranzerAdvanced Medical Bioimaging Core Facility, Charité-Universitätsmedizin , Berlin, Germany.ORCID 0000-0002-4482-7080
Martin LehmannLeibniz-Forschungsinstitut für Molekulare Pharmakologie im Forschungsverbund Berlin e.V. (FMP) , Berlin, Germany.ORCID 0000-0002-8370-6353
Jörg GroßhansDepartment of biology, Philipps-Universität Marburg, Marburg, Germany.ORCID 0000-0003-1114-9233
Stephan J SigristInstitute of Biology, Freie Universität Berlin , Berlin, Germany.ORCID 0000-0002-1698-5815

Funding

RobustCircuit FOR 5289
6 · The paper itself

Abstract

The assembly and remodeling of presynaptic specializations are of crucial importance for circuit development and adaptive behaviors. However, the mechanisms by which presynaptic material is locally distributed within synaptic terminals and across consuming active zones remain poorly understood. In this study, we identify the conserved unconventional class XV myosin, Myo15, an actin motor, as a novel regulator of presynaptic assembly and remodeling in Drosophila. Myo15 localizes to the local actin and microtubule network at synaptic terminals. Depletion of Myo15 resulted in smaller individual active zones, increased active zone density, and irregular terminal morphology, while its overexpression enlarged individual active zones and promoted synaptic terminal growth. Myo15 was found to modulate the actin meshwork, and deletion of its microtubule-binding MyTH4 domain rendered the protein nonfunctional. Furthermore, Myo15 was essential for presynaptic functional homeostatic plasticity and memory consolidation. These findings suggest that Myo15 plays a critical role in the assembly and remodeling of presynaptic active zones.

Indexed as

Drosophila melanogasterDrosophila ProteinsMyosinsPresynaptic TerminalsActinsAnimalsMicrotubulesNeuronal PlasticityActinsDrosophila ProteinsMyosins

Identifiers

PMID40627464
PMCPMC12237259

What Socratic 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 Socratic graph.