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Hunchback prevents notch-induced apoptosis in the serotonergic lineage of Drosophila Melanogaster.驼背蛋白可防止果蝇血清素能谱系中Notch诱导的细胞凋亡。
Dev Biol. 2022 Jun;486:109-120. doi: 10.1016/j.ydbio.2022.03.012. Epub 2022 Apr 4.
2
Identification of an evolutionarily conserved domain in Neurod1 favouring enteroendocrine versus goblet cell fate.鉴定 Neurod1 中一个进化上保守的结构域,有利于肠内分泌细胞而非杯状细胞的命运。
PLoS Genet. 2022 Mar 14;18(3):e1010109. doi: 10.1371/journal.pgen.1010109. eCollection 2022 Mar.
3
The Role of Neurod Genes in Brain Development, Function, and Disease.神经发育相关基因在大脑发育、功能及疾病中的作用。
Front Mol Neurosci. 2021 Jun 9;14:662774. doi: 10.3389/fnmol.2021.662774. eCollection 2021.
4
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/NeuroD1 Functions with the Homeobox Gene /Vax2 and Hox Gene /labial To Specify Aspects of RME and DD Neuron Fate in .NeuroD1 与同源盒基因 /Vax2 和 Hox 基因 /labial 一起作用,以指定. 中的 RME 和 DD 神经元命运的各个方面。
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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.

DOI:10.1002/dneu.22902
PMID:36336988
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10440801/
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。