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CACNA1C gene regulates behavioral strategies in operant rule learning
Behavioral experiments are usually designed to tap into a specific cognitive function, but animals may solve a given task through a variety of different and individual behavioral strategies, some of them not foreseen by the experimenter. Animal learning may therefore be seen more as the process of s...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5467799/ https://www.ncbi.nlm.nih.gov/pubmed/28604818 http://dx.doi.org/10.1371/journal.pbio.2000936 |
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author | Koppe, Georgia Mallien, Anne Stephanie Berger, Stefan Bartsch, Dusan Gass, Peter Vollmayr, Barbara Durstewitz, Daniel |
author_facet | Koppe, Georgia Mallien, Anne Stephanie Berger, Stefan Bartsch, Dusan Gass, Peter Vollmayr, Barbara Durstewitz, Daniel |
author_sort | Koppe, Georgia |
collection | PubMed |
description | Behavioral experiments are usually designed to tap into a specific cognitive function, but animals may solve a given task through a variety of different and individual behavioral strategies, some of them not foreseen by the experimenter. Animal learning may therefore be seen more as the process of selecting among, and adapting, potential behavioral policies, rather than mere strengthening of associative links. Calcium influx through high-voltage-gated Ca(2+) channels is central to synaptic plasticity, and altered expression of Ca(v)1.2 channels and the CACNA1C gene have been associated with severe learning deficits and psychiatric disorders. Given this, we were interested in how specifically a selective functional ablation of the Cacna1c gene would modulate the learning process. Using a detailed, individual-level analysis of learning on an operant cue discrimination task in terms of behavioral strategies, combined with Bayesian selection among computational models estimated from the empirical data, we show that a Cacna1c knockout does not impair learning in general but has a much more specific effect: the majority of Cacna1c knockout mice still managed to increase reward feedback across trials but did so by adapting an outcome-based strategy, while the majority of matched controls adopted the experimentally intended cue-association rule. Our results thus point to a quite specific role of a single gene in learning and highlight that much more mechanistic insight could be gained by examining response patterns in terms of a larger repertoire of potential behavioral strategies. The results may also have clinical implications for treating psychiatric disorders. |
format | Online Article Text |
id | pubmed-5467799 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-54677992017-06-22 CACNA1C gene regulates behavioral strategies in operant rule learning Koppe, Georgia Mallien, Anne Stephanie Berger, Stefan Bartsch, Dusan Gass, Peter Vollmayr, Barbara Durstewitz, Daniel PLoS Biol Research Article Behavioral experiments are usually designed to tap into a specific cognitive function, but animals may solve a given task through a variety of different and individual behavioral strategies, some of them not foreseen by the experimenter. Animal learning may therefore be seen more as the process of selecting among, and adapting, potential behavioral policies, rather than mere strengthening of associative links. Calcium influx through high-voltage-gated Ca(2+) channels is central to synaptic plasticity, and altered expression of Ca(v)1.2 channels and the CACNA1C gene have been associated with severe learning deficits and psychiatric disorders. Given this, we were interested in how specifically a selective functional ablation of the Cacna1c gene would modulate the learning process. Using a detailed, individual-level analysis of learning on an operant cue discrimination task in terms of behavioral strategies, combined with Bayesian selection among computational models estimated from the empirical data, we show that a Cacna1c knockout does not impair learning in general but has a much more specific effect: the majority of Cacna1c knockout mice still managed to increase reward feedback across trials but did so by adapting an outcome-based strategy, while the majority of matched controls adopted the experimentally intended cue-association rule. Our results thus point to a quite specific role of a single gene in learning and highlight that much more mechanistic insight could be gained by examining response patterns in terms of a larger repertoire of potential behavioral strategies. The results may also have clinical implications for treating psychiatric disorders. Public Library of Science 2017-06-12 /pmc/articles/PMC5467799/ /pubmed/28604818 http://dx.doi.org/10.1371/journal.pbio.2000936 Text en © 2017 Koppe 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 Koppe, Georgia Mallien, Anne Stephanie Berger, Stefan Bartsch, Dusan Gass, Peter Vollmayr, Barbara Durstewitz, Daniel CACNA1C gene regulates behavioral strategies in operant rule learning |
title | CACNA1C gene regulates behavioral strategies in operant rule learning |
title_full | CACNA1C gene regulates behavioral strategies in operant rule learning |
title_fullStr | CACNA1C gene regulates behavioral strategies in operant rule learning |
title_full_unstemmed | CACNA1C gene regulates behavioral strategies in operant rule learning |
title_short | CACNA1C gene regulates behavioral strategies in operant rule learning |
title_sort | cacna1c gene regulates behavioral strategies in operant rule learning |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5467799/ https://www.ncbi.nlm.nih.gov/pubmed/28604818 http://dx.doi.org/10.1371/journal.pbio.2000936 |
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