Cargando…
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...
Autores principales: | , , , , , , , |
---|---|
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 |
_version_ | 1784910288196206592 |
---|---|
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. |
format | Online Article Text |
id | pubmed-10030115 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT zhaojianjian geneticdissectionofmutualinterferencebetweentwoconsecutivelearningtasksindrosophila AT zhangxuchen geneticdissectionofmutualinterferencebetweentwoconsecutivelearningtasksindrosophila AT zhaobohan geneticdissectionofmutualinterferencebetweentwoconsecutivelearningtasksindrosophila AT huwantong geneticdissectionofmutualinterferencebetweentwoconsecutivelearningtasksindrosophila AT diaotongxin geneticdissectionofmutualinterferencebetweentwoconsecutivelearningtasksindrosophila AT wangliyuan geneticdissectionofmutualinterferencebetweentwoconsecutivelearningtasksindrosophila AT zhongyi geneticdissectionofmutualinterferencebetweentwoconsecutivelearningtasksindrosophila AT liqian geneticdissectionofmutualinterferencebetweentwoconsecutivelearningtasksindrosophila |