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miRNA-124 通过调控 Notch 和 NeuroD1 介导神经元发育的过渡状态。

microRNA-124 regulates Notch and NeuroD1 to mediate transition states of neuronal development.

机构信息

Department of Biological Sciences, University of Delaware, Newark, Delaware, USA.

出版信息

Dev Neurobiol. 2023 Jan;83(1-2):3-27. doi: 10.1002/dneu.22902. Epub 2022 Nov 23.

Abstract

MicroRNAs regulate gene expression by destabilizing target mRNA and/or inhibiting translation in animal cells. The ability to mechanistically dissect miR-124's function during specification, differentiation, and maturation of neurons during development within a single system has not been accomplished. Using the sea urchin embryo, we take advantage of the manipulability of the embryo and its well-documented gene regulatory networks (GRNs). We incorporated NeuroD1 as part of the sea urchin neuronal GRN and determined that miR-124 inhibition resulted in aberrant gut contractions, swimming velocity, and neuronal development. Inhibition of miR-124 resulted in an increased number of cells expressing transcription factors (TFs) associated with progenitor neurons and a concurrent decrease of mature and functional neurons. Results revealed that in the early blastula/gastrula stages, miR-124 regulates undefined factors during neuronal specification and differentiation. In the late gastrula/larval stages, miR-124 regulates Notch and NeuroD1 during the transition between neuronal differentiation and maturation. Overall, we have improved the neuronal GRN and identified miR-124 to play a prolific role in regulating various transitions of neuronal development.

摘要

MicroRNAs 通过使靶 mRNA 不稳定和/或抑制翻译来调节基因表达。在单个系统中,尚未完成在发育过程中对神经元的特化、分化和成熟过程中 miR-124 的功能进行机制剖析的能力。利用海胆胚胎,我们利用胚胎的可操作性及其经过充分记录的基因调控网络 (GRN)。我们将 NeuroD1 作为海胆神经元 GRN 的一部分,并确定 miR-124 的抑制导致肠道收缩、游泳速度和神经元发育异常。miR-124 的抑制导致与祖细胞神经元相关的转录因子 (TF) 的表达细胞数量增加,而成熟和功能神经元的数量减少。结果表明,在早期囊胚/原肠胚阶段,miR-124 在神经元特化和分化过程中调节未定义的因子。在晚期原肠胚/幼虫阶段,miR-124 在神经元分化和成熟之间的过渡过程中调节 Notch 和 NeuroD1。总的来说,我们改进了神经元 GRN,并确定 miR-124 在调节神经元发育的各种转变中发挥了重要作用。

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