Evidence map›Paper›PMID 41162381›Full record

ArticleNature communications2025

A memory transcriptome time course reveals essential long-term memory transcription factors.

Spencer G Jones, Beatriz Gil-Martí, Eva Sacristán-Horcajada, Abigail C Edison, Emily F Butler, Neda Miandashti, Camilla Roselli, Enrique Turiégano, Tamara Boto, Jamie M Kramer and 1 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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Cell-type-specific circadian and light-responsive transcriptional dynamics in adultProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. 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

11 authors.

Spencer G Jones *Biochemistry and Molecular Biology, Dalhousie University, Halifax, NS, Canada.ORCID http://orcid.org/0000-0002-0584-526X
Beatriz Gil-Martí *Cajal Institute, Spanish National Research Council (CSIC), Madrid, Spain.ORCID http://orcid.org/0000-0001-6512-0925
Eva Sacristán-HorcajadaBiocomputational Analysis Core Facility, Centro de Biología Molecular Severo Ochoa, Spanish National Research Council (CSIC), Madrid, Spain.
Abigail C EdisonBiochemistry and Molecular Biology, Dalhousie University, Halifax, NS, Canada.
Emily F ButlerBiochemistry and Molecular Biology, Dalhousie University, Halifax, NS, Canada.ORCID http://orcid.org/0009-0007-9917-2345
Neda MiandashtiBiochemistry and Molecular Biology, Dalhousie University, Halifax, NS, Canada.
Camilla RoselliDepartment of Genetics and Microbiology, Trinity College Dublin, Dublin 2, Ireland.ORCID http://orcid.org/0000-0002-2272-980X
Enrique TuriéganoDepartment of Biology, Autonomous University of Madrid, Madrid, Spain.
Tamara BotoTrinity College Institute of Neuroscience, Trinity College Dublin, Dublin 2, Ireland.ORCID http://orcid.org/0000-0002-9974-3714
Jamie M Kramer *Biochemistry and Molecular Biology, Dalhousie University, Halifax, NS, Canada. jkramer@dal.ca.ORCID http://orcid.org/0000-0002-0924-1279
Francisco A Martin *Cajal Institute, Spanish National Research Council (CSIC), Madrid, Spain. fmarti22@ucm.es.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long-term memory (LTM) requires transcription and translation of new proteins, yet the transcriptional control of memory remains poorly understood. Here, we performed a transcriptome time-course during LTM formation in Drosophila melanogaster exposed to courtship conditioning. We identified a mushroom body-specific transcriptional memory trace that becomes activated during memory consolidation. Using scRNAseq of CREB-activated cells we were able to detect a persistent transcriptional response in MB neurons after LTM consolidation and retrieval. As a proof of causality, we conducted a loss-of-function screen for genes comprising the transcriptional memory trace, finding 16 positive hits whose disruption impaired LTM. Among them, we identified two neuron activity-regulated genes, Hr38 and sr, which encode transcription factors that are activated by courtship LTM training, required for LTM, and bind to many genes comprising the transcriptional memory trace. Overall, we further define the transcriptional response to LTM and identify transcription factors that may help shape it.

Indexed as

Drosophila melanogasterDrosophila ProteinsMemory, Long-TermTranscription FactorsTranscriptomeAnimalsCourtshipCyclic AMP Response Element-Binding ProteinFemaleGene Expression RegulationMaleMushroom BodiesNeuronsCyclic AMP Response Element-Binding ProteinDrosophila ProteinsTranscription Factors

Identifiers

PMID41162381
PMCPMC12572301

What OpenQuestion holds

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LicenceCC BY
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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.