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Genetic Dissection of Aversive Associative Olfactory Learning and Memory in Drosophila Larvae

Memory formation is a highly complex and dynamic process. It consists of different phases, which depend on various neuronal and molecular mechanisms. In adult Drosophila it was shown that memory formation after aversive Pavlovian conditioning includes—besides other forms—a labile short-term componen...

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Autores principales: Widmann, Annekathrin, Artinger, Marc, Biesinger, Lukas, Boepple, Kathrin, Peters, Christina, Schlechter, Jana, Selcho, Mareike, Thum, Andreas S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5074598/
https://www.ncbi.nlm.nih.gov/pubmed/27768692
http://dx.doi.org/10.1371/journal.pgen.1006378
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author Widmann, Annekathrin
Artinger, Marc
Biesinger, Lukas
Boepple, Kathrin
Peters, Christina
Schlechter, Jana
Selcho, Mareike
Thum, Andreas S.
author_facet Widmann, Annekathrin
Artinger, Marc
Biesinger, Lukas
Boepple, Kathrin
Peters, Christina
Schlechter, Jana
Selcho, Mareike
Thum, Andreas S.
author_sort Widmann, Annekathrin
collection PubMed
description Memory formation is a highly complex and dynamic process. It consists of different phases, which depend on various neuronal and molecular mechanisms. In adult Drosophila it was shown that memory formation after aversive Pavlovian conditioning includes—besides other forms—a labile short-term component that consolidates within hours to a longer-lasting memory. Accordingly, memory formation requires the timely controlled action of different neuronal circuits, neurotransmitters, neuromodulators and molecules that were initially identified by classical forward genetic approaches. Compared to adult Drosophila, memory formation was only sporadically analyzed at its larval stage. Here we deconstruct the larval mnemonic organization after aversive olfactory conditioning. We show that after odor-high salt conditioning larvae form two parallel memory phases; a short lasting component that depends on cyclic adenosine 3’5’-monophosphate (cAMP) signaling and synapsin gene function. In addition, we show for the first time for Drosophila larvae an anesthesia resistant component, which relies on radish and bruchpilot gene function, protein kinase C activity, requires presynaptic output of mushroom body Kenyon cells and dopamine function. Given the numerical simplicity of the larval nervous system this work offers a unique prospect for studying memory formation of defined specifications, at full-brain scope with single-cell, and single-synapse resolution.
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spelling pubmed-50745982016-11-04 Genetic Dissection of Aversive Associative Olfactory Learning and Memory in Drosophila Larvae Widmann, Annekathrin Artinger, Marc Biesinger, Lukas Boepple, Kathrin Peters, Christina Schlechter, Jana Selcho, Mareike Thum, Andreas S. PLoS Genet Research Article Memory formation is a highly complex and dynamic process. It consists of different phases, which depend on various neuronal and molecular mechanisms. In adult Drosophila it was shown that memory formation after aversive Pavlovian conditioning includes—besides other forms—a labile short-term component that consolidates within hours to a longer-lasting memory. Accordingly, memory formation requires the timely controlled action of different neuronal circuits, neurotransmitters, neuromodulators and molecules that were initially identified by classical forward genetic approaches. Compared to adult Drosophila, memory formation was only sporadically analyzed at its larval stage. Here we deconstruct the larval mnemonic organization after aversive olfactory conditioning. We show that after odor-high salt conditioning larvae form two parallel memory phases; a short lasting component that depends on cyclic adenosine 3’5’-monophosphate (cAMP) signaling and synapsin gene function. In addition, we show for the first time for Drosophila larvae an anesthesia resistant component, which relies on radish and bruchpilot gene function, protein kinase C activity, requires presynaptic output of mushroom body Kenyon cells and dopamine function. Given the numerical simplicity of the larval nervous system this work offers a unique prospect for studying memory formation of defined specifications, at full-brain scope with single-cell, and single-synapse resolution. Public Library of Science 2016-10-21 /pmc/articles/PMC5074598/ /pubmed/27768692 http://dx.doi.org/10.1371/journal.pgen.1006378 Text en © 2016 Widmann et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Widmann, Annekathrin
Artinger, Marc
Biesinger, Lukas
Boepple, Kathrin
Peters, Christina
Schlechter, Jana
Selcho, Mareike
Thum, Andreas S.
Genetic Dissection of Aversive Associative Olfactory Learning and Memory in Drosophila Larvae
title Genetic Dissection of Aversive Associative Olfactory Learning and Memory in Drosophila Larvae
title_full Genetic Dissection of Aversive Associative Olfactory Learning and Memory in Drosophila Larvae
title_fullStr Genetic Dissection of Aversive Associative Olfactory Learning and Memory in Drosophila Larvae
title_full_unstemmed Genetic Dissection of Aversive Associative Olfactory Learning and Memory in Drosophila Larvae
title_short Genetic Dissection of Aversive Associative Olfactory Learning and Memory in Drosophila Larvae
title_sort genetic dissection of aversive associative olfactory learning and memory in drosophila larvae
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5074598/
https://www.ncbi.nlm.nih.gov/pubmed/27768692
http://dx.doi.org/10.1371/journal.pgen.1006378
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