Evidence map›Paper›PMID 42213044›Full record

ArticleGenetics2026

Amyloid precursor protein ortholog Appl acts with Vnd during mushroom body axon growth in Drosophila.

Claire Marquilly, Germain U Busto, Laure Pasquer, Robert P Zinzen, Bassem A Hassan, Lee G Fradkin, Thomas Preat, Ana Boulanger, Jean-Maurice Dura

Abstract read
In one paragraph

Article in Genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Claire MarquillyIGH, Univ Montpellier, CNRS, 141 rue de la Cardonille, Montpellier 34396, France.
Germain U BustoIGH, Univ Montpellier, CNRS, 141 rue de la Cardonille, Montpellier 34396, France.
Laure PasquerBrain Plasticity Unit, CNRS, ESPCI Paris, PSL Research University, 10 rue Vauquelin, Paris 75005, France.
Robert P ZinzenMax Delbrück Centrum für moleculare Medizin in der Helmholtz Gemeinschaft (MDC), BIMSB, Robert-Rössle-Straβe 10, Berlin 13125, Germany.
Bassem A HassanInstitut du Cerveau-Paris Brain Institute (ICM), Sorbonne Université, Inserm, CNRS, Hôpital Pitié-Salpêtrière, 47 Boulevard de l'Hôpital, Paris 75013, France.
Lee G FradkinInstitute for Stem Cell Biology and Regenerative Medicine, Lokey Stem Cell Research Building (SIM1), Stanford University Medical School, Stanford University, 265 Campus Drive, 3rd Floor, Stanford, CA 94305, United States.
Thomas PreatBrain Plasticity Unit, CNRS, ESPCI Paris, PSL Research University, 10 rue Vauquelin, Paris 75005, France.
Ana BoulangerIGH, Univ Montpellier, CNRS, 141 rue de la Cardonille, Montpellier 34396, France.
Jean-Maurice DuraIGH, Univ Montpellier, CNRS, 141 rue de la Cardonille, Montpellier 34396, France.ORCID 0000-0001-8296-9023

Funding

Agence Nationale de la Recherche ANR-21-CE16-0033-ORIOAgence Nationale de la Recherche ANR-24-CE16-5161-ExOrionAssociation pour la Recherche sur le Cancer PJA 20151203422Centre National de la Recherche ScientifiqueFondation Langlois and the Fondation pour la Recherche Médicale MND202411019909)Fondation pour la Recherche MédicaleMinistère de l'Enseignement Supérieur et de la Recherche
6 · The paper itself

Abstract

The amyloid precursor protein (APP) is associated with Alzheimer's disease. Appl is the single Drosophila APP ortholog and is expressed in all neurons throughout development. Appl was previously shown to cell-autonomously modulate axon outgrowth in the mushroom bodies (MBs), the fly olfactory memory center. However, we found that Appld, the only reported null allele, affects the normal function of vnd, the gene just proximal to Appl. To decipher developmental and memory defects specifically due to a loss of only Appl function, we generated a precise Appl null allele (ApplC2.1) by CRISPR/Cas9 genomic engineering. With ApplC2.1, we confirmed the partial contribution for Appl in MB axon outgrowth. We also produced new CRISPR vnd alleles removing either vnd-B or vnd-A function. We report here that vnd is also required for MB β-branch axon outgrowth and to a much greater extent than Appl itself. Moreover, vnd is expressed in neurons close to, but not within, the MB during development and is required non-cell-autonomously for MB axon outgrowth. It was previously shown that Appl knockdown in the MBs results in loss of memory following the association of odorants with electric shocks. Differently from Appld flies we found no defects of electric shock avoidance in ApplC2.1 flies, allowing us to test for memory. ApplC2.1 flies showed a complete loss of long-term memory which was fully rescued by MB-restricted expression of Appl+ only during the adult stage. Therefore, we demonstrate that the complete lack of Appl affects memory independently from structural developmental defects.

Indexed as

Adaptor Proteins, Signal TransducingAmyloid beta-Protein PrecursorAxonsDrosophila ProteinsMushroom BodiesNerve Tissue ProteinsAnimalsDrosophila melanogasterMembrane ProteinsAdaptor Proteins, Signal TransducingAmyloid beta-Protein PrecursorAppl protein, DrosophilaDrosophila ProteinsMembrane ProteinsNerve Tissue ProteinsAppl nullaversive long-term memoryaxon growthbrain developmentCRISPRmushroom bodyVnd-A nullVnd-Appl signalingVnd-B null

Identifiers

PMID42213044
PMCPMC13334118

What Socratic holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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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.