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Genetic dissection of mutual interference between two consecutive learning tasks in Drosophila

Animals can continuously learn different tasks to adapt to changing environments and, therefore, have strategies to effectively cope with inter-task interference, including both proactive interference (Pro-I) and retroactive interference (Retro-I). Many biological mechanisms are known to contribute...

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Autores principales: Zhao, Jianjian, Zhang, Xuchen, Zhao, Bohan, Hu, Wantong, Diao, Tongxin, Wang, Liyuan, Zhong, Yi, Li, Qian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10030115/
https://www.ncbi.nlm.nih.gov/pubmed/36897069
http://dx.doi.org/10.7554/eLife.83516
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author Zhao, Jianjian
Zhang, Xuchen
Zhao, Bohan
Hu, Wantong
Diao, Tongxin
Wang, Liyuan
Zhong, Yi
Li, Qian
author_facet Zhao, Jianjian
Zhang, Xuchen
Zhao, Bohan
Hu, Wantong
Diao, Tongxin
Wang, Liyuan
Zhong, Yi
Li, Qian
author_sort Zhao, Jianjian
collection PubMed
description Animals can continuously learn different tasks to adapt to changing environments and, therefore, have strategies to effectively cope with inter-task interference, including both proactive interference (Pro-I) and retroactive interference (Retro-I). Many biological mechanisms are known to contribute to learning, memory, and forgetting for a single task, however, mechanisms involved only when learning sequential different tasks are relatively poorly understood. Here, we dissect the respective molecular mechanisms of Pro-I and Retro-I between two consecutive associative learning tasks in Drosophila. Pro-I is more sensitive to an inter-task interval (ITI) than Retro-I. They occur together at short ITI (<20 min), while only Retro-I remains significant at ITI beyond 20 min. Acutely overexpressing Corkscrew (CSW), an evolutionarily conserved protein tyrosine phosphatase SHP2, in mushroom body (MB) neurons reduces Pro-I, whereas acute knockdown of CSW exacerbates Pro-I. Such function of CSW is further found to rely on the γ subset of MB neurons and the downstream Raf/MAPK pathway. In contrast, manipulating CSW does not affect Retro-I as well as a single learning task. Interestingly, manipulation of Rac1, a molecule that regulates Retro-I, does not affect Pro-I. Thus, our findings suggest that learning different tasks consecutively triggers distinct molecular mechanisms to tune proactive and retroactive interference.
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spelling pubmed-100301152023-03-22 Genetic dissection of mutual interference between two consecutive learning tasks in Drosophila Zhao, Jianjian Zhang, Xuchen Zhao, Bohan Hu, Wantong Diao, Tongxin Wang, Liyuan Zhong, Yi Li, Qian eLife Neuroscience Animals can continuously learn different tasks to adapt to changing environments and, therefore, have strategies to effectively cope with inter-task interference, including both proactive interference (Pro-I) and retroactive interference (Retro-I). Many biological mechanisms are known to contribute to learning, memory, and forgetting for a single task, however, mechanisms involved only when learning sequential different tasks are relatively poorly understood. Here, we dissect the respective molecular mechanisms of Pro-I and Retro-I between two consecutive associative learning tasks in Drosophila. Pro-I is more sensitive to an inter-task interval (ITI) than Retro-I. They occur together at short ITI (<20 min), while only Retro-I remains significant at ITI beyond 20 min. Acutely overexpressing Corkscrew (CSW), an evolutionarily conserved protein tyrosine phosphatase SHP2, in mushroom body (MB) neurons reduces Pro-I, whereas acute knockdown of CSW exacerbates Pro-I. Such function of CSW is further found to rely on the γ subset of MB neurons and the downstream Raf/MAPK pathway. In contrast, manipulating CSW does not affect Retro-I as well as a single learning task. Interestingly, manipulation of Rac1, a molecule that regulates Retro-I, does not affect Pro-I. Thus, our findings suggest that learning different tasks consecutively triggers distinct molecular mechanisms to tune proactive and retroactive interference. eLife Sciences Publications, Ltd 2023-03-10 /pmc/articles/PMC10030115/ /pubmed/36897069 http://dx.doi.org/10.7554/eLife.83516 Text en © 2023, Zhao et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Zhao, Jianjian
Zhang, Xuchen
Zhao, Bohan
Hu, Wantong
Diao, Tongxin
Wang, Liyuan
Zhong, Yi
Li, Qian
Genetic dissection of mutual interference between two consecutive learning tasks in Drosophila
title Genetic dissection of mutual interference between two consecutive learning tasks in Drosophila
title_full Genetic dissection of mutual interference between two consecutive learning tasks in Drosophila
title_fullStr Genetic dissection of mutual interference between two consecutive learning tasks in Drosophila
title_full_unstemmed Genetic dissection of mutual interference between two consecutive learning tasks in Drosophila
title_short Genetic dissection of mutual interference between two consecutive learning tasks in Drosophila
title_sort genetic dissection of mutual interference between two consecutive learning tasks in drosophila
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10030115/
https://www.ncbi.nlm.nih.gov/pubmed/36897069
http://dx.doi.org/10.7554/eLife.83516
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