FB2026_01 , released March 12, 2026
FB2026_01 , released March 12, 2026
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Citation
Jones, S.G., Gil-Martí, B., Sacristán-Horcajada, E., Edison, A.C., Butler, E.F., Miandashti, N., Roselli, C., Turiégano, E., Boto, T., Kramer, J.M., Martin, F.A. (2025). A memory transcriptome time course reveals essential long-term memory transcription factors.  Nat. Commun. 16(1): 9320.
FlyBase ID
FBrf0263729
Publication Type
Research paper
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.
PubMed ID
PubMed Central ID
PMC12572301 (PMC) (EuropePMC)
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Secondary IDs
    Language of Publication
    English
    Additional Languages of Abstract
    Parent Publication
    Publication Type
    Journal
    Abbreviation
    Nat. Commun.
    Title
    Nature communications
    ISBN/ISSN
    2041-1723
    Data From Reference