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在 中,对两个连续学习任务之间的相互干扰进行遗传剖析。

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

机构信息

School of Life Sciences, IDG/McGovern Institute for Brain Research, MOE Key Laboratory of Protein Sciences, Tsinghua University, Beijing, China.

Tsinghua-Peking Center for Life Sciences, Beijing, China.

出版信息

Elife. 2023 Mar 10;12:e83516. doi: 10.7554/eLife.83516.

Abstract

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 . 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.

摘要

动物可以不断学习不同的任务,以适应不断变化的环境,因此它们有策略来有效地应对任务间干扰,包括前摄干扰(Pro-I)和回溯干扰(Retro-I)。许多已知的生物学机制有助于单一任务的学习、记忆和遗忘,然而,当学习连续的不同任务时,涉及的机制相对了解较少。在这里,我们在. 中剖析了两个连续的联想学习任务之间的 Pro-I 和 Retro-I 的各自分子机制。Pro-I 比 Retro-I 对任务间间隔(ITI)更敏感。它们在短 ITI(<20 分钟)时一起发生,而只有 Retro-I 在 ITI 超过 20 分钟时仍然显著。急性过表达蘑菇体(MB)神经元中进化保守的蛋白酪氨酸磷酸酶 SHP2 的 Corkscrew(CSW),可减少 Pro-I,而急性敲低 CSW 则加剧 Pro-I。CSW 的这种功能进一步被发现依赖于 MB 神经元的γ亚群和下游的 Raf/MAPK 途径。相比之下,操纵 CSW 既不影响 Retro-I,也不影响单一的学习任务。有趣的是,操纵 Rac1(一种调节 Retro-I 的分子)并不影响 Pro-I。因此,我们的研究结果表明,连续学习不同的任务会触发不同的分子机制来调节前摄和回溯干扰。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f978/10030115/0fa3a3818dd1/elife-83516-fig1.jpg

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