Evidence map›Paper›PMID 39747038›Full record

ArticleNature communications2025

Blobby is a synaptic active zone assembly protein required for memory in Drosophila.

J Lützkendorf, T Matkovic-Rachid, S Liu, T Götz, L Gao, O Turrel, M Maglione, M Grieger, S Putignano, N Ramesh and 14 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

24 authors.

J Lützkendorf *Freie Universität Berlin, Institute for Biology and Genetics, Berlin, Germany.ORCID 0000-0001-5051-6281
T Matkovic-Rachid *Freie Universität Berlin, Institute for Biology and Genetics, Berlin, Germany.
S LiuFreie Universität Berlin, Institute of Chemistry and Biochemistry/Structural Biochemistry, Berlin, Germany.
T GötzFreie Universität Berlin, Institute for Biology and Genetics, Berlin, Germany.
L GaoFreie Universität Berlin, Institute for Biology and Genetics, Berlin, Germany.
O TurrelFreie Universität Berlin, Institute for Biology and Genetics, Berlin, Germany.ORCID 0000-0003-2174-7659
M MaglioneFreie Universität Berlin, Institute for Biology and Genetics, Berlin, Germany.ORCID 0000-0001-9052-9271
M GriegerFreie Universität Berlin, Institute for Biology and Genetics, Berlin, Germany.
S PutignanoFreie Universität Berlin, Institute for Biology and Genetics, Berlin, Germany.
N RameshFreie Universität Berlin, Institute for Biology and Genetics, Berlin, Germany.ORCID 0000-0002-7099-4093
T GhelaniFreie Universität Berlin, Institute for Biology and Genetics, Berlin, Germany.ORCID 0000-0003-1835-4686
A NeumannFreie Universität Berlin, Institute for Biology and Genetics, Berlin, Germany.
N GimberCharité- Universitätsmedizin, Advanced Medical Bioimaging Core Facility, Berlin, Germany.ORCID 0000-0001-9456-3063
J SchmoranzerCharité- Universitätsmedizin, Advanced Medical Bioimaging Core Facility, Berlin, Germany.
A StawrakakisFreie Universität Berlin, Institute for Biology and Genetics, Berlin, Germany.
B BrenceZuse Institute Berlin, Department of Visual and Data-Centric Computing, Berlin, Germany.
D BaumZuse Institute Berlin, Department of Visual and Data-Centric Computing, Berlin, Germany.ORCID 0000-0003-1550-7245
Kai LudwigFreie Universität Berlin, Institut für Chemie and Biochemie, Forschungszentrum für Elektronenmikroskopie, Berlin, Germany.ORCID 0000-0001-6808-8107
M HeineInstitute of Developmental Biology and Neurobiology, Johannes Gutenberg University Mainz, Mainz, Germany.
T MielkeMax Planck Institute for Molecular Genetics, Berlin, Microscopy and Cryo-Electron Microscopy Service Group, Berlin, Germany.ORCID 0000-0001-9275-3146
F LiuLeibniz-Forschungsinstitut für Molekulare Pharmakologie, Campus Berlin-Buch, Berlin, Germany.ORCID 0000-0002-2358-549X
A M WalterLeibniz-Forschungsinstitut für Molekulare Pharmakologie, Campus Berlin-Buch, Berlin, Germany.ORCID 0000-0001-5646-4750
M C WahlFreie Universität Berlin, Institute of Chemistry and Biochemistry/Structural Biochemistry, Berlin, Germany.ORCID 0000-0002-2811-5307
S J SigristFreie Universität Berlin, Institute for Biology and Genetics, Berlin, Germany. stephan.sigrist@fu-berlin.de.ORCID 0000-0002-1698-5815

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) CRC1315/A08 (project ID 327654276)Deutsche Forschungsgemeinschaft (German Research Foundation) Excellence Cluster Neurocure (EXC-2049-390688087)Deutsche Forschungsgemeinschaft (German Research Foundation) FOR2705 (project ID 365082554)Deutsche Forschungsgemeinschaft (German Research Foundation) FOR5228 (project ID 447288260)Deutsche Forschungsgemeinschaft (German Research Foundation) FOR5289 (project ID 453877723)Deutsche Forschungsgemeinschaft (German Research Foundation) NeuroNex2 (project ID 436260754)Deutsche Forschungsgemeinschaft (German Research Foundation) Transregio SFB 186 (project ID 278001972)Novo Nordisk Fonden (Novo Nordisk Foundation) Young Investigator Award (project ID NNF19OC0056047)
6 · The paper itself

Abstract

At presynaptic active zones (AZs), scaffold proteins are critical for coordinating synaptic vesicle release and forming essential nanoarchitectures. However, regulatory principles steering AZ scaffold assembly, function, and plasticity remain insufficiently understood. We here identify an additional Drosophila AZ protein, "Blobby", essential for proper AZ nano-organization. Blobby biochemically associates with the ELKS family AZ scaffold protein Bruchpilot (BRP) and integrates into newly forming AZs. Loss of Blobby results in fewer AZs forming, ectopic AZ scaffold protein accumulations ("blobs") and disrupts nanoscale architecture of the BRP-AZ scaffold. Functionally, blobby mutants show diminished evoked synaptic currents due to reduced synaptic vesicle release probability and fewer functional release sites. Blobby is also present in adult brain synapses, and post-developmental knockdown of Blobby in the mushroom body impairs olfactory aversive memory consolidation. Thus, our analysis identifies an additional layer of AZ regulation critical for developmental AZ assembly but also for AZ-mediated plasticity controlling behavior.

Indexed as

Drosophila melanogasterDrosophila ProteinsMemoryMushroom BodiesSynaptic VesiclesAnimalsBrainMutationNeuronal PlasticityPresynaptic TerminalsSynapsesSynaptic TransmissionBRP protein, DrosophilaDrosophila Proteins

Identifiers

PMID39747038
PMCPMC11696761

What OpenQuestion holds

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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 OpenQuestion graph.