Consolidation and maintenance of long-term memory involve dual functions of the developmental regulator Apterous in clock neurons and mushroom bodies in the Drosophila brain.
Animals
Biological Clocks
/ physiology
Brain
/ physiology
Drosophila Proteins
/ genetics
Drosophila melanogaster
/ physiology
Heterozygote
LIM-Homeodomain Proteins
/ genetics
Memory Consolidation
/ physiology
Memory, Long-Term
/ physiology
Models, Biological
Mushroom Bodies
/ physiology
Mutation
/ genetics
Neurons
/ physiology
Phenotype
Synaptic Transmission
/ physiology
Transcription Factors
/ genetics
gamma-Aminobutyric Acid
/ pharmacology
Journal
PLoS biology
ISSN: 1545-7885
Titre abrégé: PLoS Biol
Pays: United States
ID NLM: 101183755
Informations de publication
Date de publication:
12 2021
12 2021
Historique:
received:
21
10
2020
accepted:
25
10
2021
entrez:
3
12
2021
pubmed:
4
12
2021
medline:
24
12
2021
Statut:
epublish
Résumé
Memory is initially labile but can be consolidated into stable long-term memory (LTM) that is stored in the brain for extended periods. Despite recent progress, the molecular and cellular mechanisms underlying the intriguing neurobiological processes of LTM remain incompletely understood. Using the Drosophila courtship conditioning assay as a memory paradigm, here, we show that the LIM homeodomain (LIM-HD) transcription factor Apterous (Ap), which is known to regulate various developmental events, is required for both the consolidation and maintenance of LTM. Interestingly, Ap is involved in these 2 memory processes through distinct mechanisms in different neuronal subsets in the adult brain. Ap and its cofactor Chip (Chi) are indispensable for LTM maintenance in the Drosophila memory center, the mushroom bodies (MBs). On the other hand, Ap plays a crucial role in memory consolidation in a Chi-independent manner in pigment dispersing factor (Pdf)-containing large ventral-lateral clock neurons (l-LNvs) that modulate behavioral arousal and sleep. Since disrupted neurotransmission and electrical silencing in clock neurons impair memory consolidation, Ap is suggested to contribute to the stabilization of memory by ensuring the excitability of l-LNvs. Indeed, ex vivo imaging revealed that a reduced function of Ap, but not Chi, results in exaggerated Cl- responses to the inhibitory neurotransmitter gamma-aminobutyric acid (GABA) in l-LNvs, indicating that wild-type (WT) Ap maintains high l-LNv excitability by suppressing the GABA response. Consistently, enhancing the excitability of l-LNvs by knocking down GABAA receptors compensates for the impaired memory consolidation in ap null mutants. Overall, our results revealed unique dual functions of the developmental regulator Ap for LTM consolidation in clock neurons and LTM maintenance in MBs.
Identifiants
pubmed: 34860826
doi: 10.1371/journal.pbio.3001459
pii: PBIOLOGY-D-20-03123
pmc: PMC8641882
doi:
Substances chimiques
Drosophila Proteins
0
LIM-Homeodomain Proteins
0
Transcription Factors
0
ap protein, Drosophila
0
gamma-Aminobutyric Acid
56-12-2
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e3001459Déclaration de conflit d'intérêts
The authors have declared that no competing interests exist.
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