并非所有 IEG 都是相同的--记忆烙印中的分子排序。

Q3 Neuroscience Advances in neurobiology Pub Date : 2024-01-01 DOI:10.1007/978-3-031-62983-9_6
Tushar D Yelhekar, Meizhen Meng, Joslyn Doupe, Yingxi Lin
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引用次数: 0

摘要

当神经元被招募形成记忆烙印时,它们会被驱动激活一系列即时早期基因(IEGs)的表达。虽然这些 IEGs 被不加区分地用于识别所谓的记忆片段神经元,但最近的研究表明,在记忆片段中,不同的 IEG 组合在物理和功能上是不同的。记忆刻痕的这种内在异质性是由不同 IEG 的功能和分布的多样性驱动的。我们将这一过程称为分子排序,它类似于将整个记忆片段神经元群排序为由不同 IEG 分子定义的不同子记忆片段。在本章中,我们将通过系统回顾已发表的有关由以下四种主要 IEGs 定义的恩格拉集合细胞的研究成果来描述分子分拣过程:Fos、Npas4、Arc 和 Egr1。我们希望通过比较和对比记忆印记的这些可能不同的组成部分,更好地理解记忆功能分子排序过程背后的逻辑和意义。
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All IEGs Are Not Created Equal-Molecular Sorting Within the Memory Engram.

When neurons are recruited to form the memory engram, they are driven to activate the expression of a series of immediate-early genes (IEGs). While these IEGs have been used relatively indiscriminately to identify the so-called engram neurons, recent research has demonstrated that different IEG ensembles can be physically and functionally distinct within the memory engram. This inherent heterogeneity of the memory engram is driven by the diversity in the functions and distributions of different IEGs. This process, which we call molecular sorting, is analogous to sorting the entire population of engram neurons into different sub-engrams molecularly defined by different IEGs. In this chapter, we will describe the molecular sorting process by systematically reviewing published work on engram ensemble cells defined by the following four major IEGs: Fos, Npas4, Arc, and Egr1. By comparing and contrasting these likely different components of the memory engram, we hope to gain a better understanding of the logic and significance behind the molecular sorting process for memory functions.

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来源期刊
Advances in neurobiology
Advances in neurobiology Neuroscience-Neurology
CiteScore
2.80
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