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Examining Recall Memory in Infancy and Early Childhood Using the Elicited Imitation Paradigm
Published on: April 28, 2016
Selective suppression and recall of long-term memories in Drosophila
Dominique Siegenthaler1, Benjamin Escribano1, Vanessa Bräuler1
1Division of Neurobiology and Zoology, University of Kaiserslautern, Kaiserslautern, Germany.
Abstract:
Adaptive decision-making depends on the formation of novel memories. In Drosophila, the mushroom body (MB) is the site of associative olfactory long-term memory (LTM) storage. However, due to the sparse and stochastic representation of olfactory information in Kenyon cells (KCs), genetic access to individual LTMs remains elusive. Here, we develop a cAMP response element (CRE)-activity-dependent memory engram label (CAMEL) tool that genetically tags KCs responding to the conditioned stimulus (CS). CAMEL activity depends on protein-synthesis-dependent aversive LTM conditioning and reflects the time course of CRE binding protein 2 (CREB2) activity during natural memory formation. We demonstrate that inhibition of LTM-induced CAMEL neurons reduces memory expression and that artificial optogenetic reactivation is sufficient to evoke aversive behavior phenocopying memory recall. Together, our data are consistent with CAMEL neurons marking a subset of engram KCs encoding individual memories. This study provides new insights into memory circuitry organization and an entry point towards cellular and molecular understanding of LTM storage.
Insights
Researchers developed a new tool to tag memory engrams in fruit flies. This tool helps identify specific neurons involved in long-term memory, offering insights into memory storage mechanisms.
Area of Science:
- Neuroscience
- Molecular Biology
- Genetics
Background:
- Adaptive decision-making relies on forming new memories.
- The Drosophila mushroom body (MB) is crucial for storing olfactory long-term memories (LTM).
- Sparse neural representations in Kenyon cells (KCs) hinder genetic access to individual LTMs.
Purpose of the Study:
- To develop a genetic tool for labeling memory engrams in Drosophila KCs.
- To investigate the cellular basis of LTM storage in the MB.
- To explore the role of specific KC populations in memory recall.
Main Methods:
- Development of a cAMP response element (CRE)-activity-dependent memory engram label (CAMEL) tool.
- Utilizing protein-synthesis-dependent aversive LTM conditioning in Drosophila.
- Employing optogenetic techniques to manipulate CAMEL-labeled neurons.
Main Results:
- CAMEL successfully tags KCs activated by the conditioned stimulus (CS) during LTM formation.
- CAMEL activity correlates with CRE binding protein 2 (CREB2) activity during memory formation.
- Inhibiting CAMEL neurons impairs memory expression, while optogenetic reactivation elicits memory recall behavior.
Conclusions:
- CAMEL neurons mark a subset of engram KCs encoding individual memories.
- This study provides a method to access and study LTM engrams at the cellular level.
- Findings offer insights into memory circuitry organization and LTM storage mechanisms.
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