利用谱系决定因子Olig2和Sox10探索少突胶质细胞发育的转录调控

IF 2.7 4区 医学 Q2 DEVELOPMENTAL BIOLOGY
Elisabeth Sock, Michael Wegner
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引用次数: 22

摘要

转录因子Olig2和Sox10共同定义少突胶质的同一性。由于它们在发育和分化状态中持续存在,它们在任何时候都形成了少突胶质调节网络。在这篇综述中,我们利用它们的突出作用和无所不在来阐述在少突胶质细胞中组织基因调控网络的核心原则,使其保持其身份,但同时允许定义和刺激依赖性的变化,从而导致有序的谱系进展、分化和髓鞘形成。为此,我们概述了少突胶质细胞前体和Tcf7l2、Sip1、Nkx2.2、Zfp24和Myrf在分化和髓鞘形成过程中与其他转录因子(如Hes5、Id和SoxD蛋白)的多种功能和物理相互作用以及复杂的交叉调控关系,并在调控网络的背景下进行了解释。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Using the lineage determinants Olig2 and Sox10 to explore transcriptional regulation of oligodendrocyte development

Using the lineage determinants Olig2 and Sox10 to explore transcriptional regulation of oligodendrocyte development

The transcription factors Olig2 and Sox10 jointly define oligodendroglial identity. Because of their continuous presence during development and in the differentiated state they shape the oligodendroglial regulatory network at all times. In this review, we exploit their eminent role and omnipresence to elaborate the central principles that organize the gene regulatory network in oligodendrocytes in such a way that it preserves its identity, but at the same time allows defined and stimulus-dependent changes that result in an ordered lineage progression, differentiation, and myelination. For this purpose, we outline the multiple functional and physical interactions and intricate cross-regulatory relationships with other transcription factors, such as Hes5, Id, and SoxD proteins, in oligodendrocyte precursors and Tcf7l2, Sip1, Nkx2.2, Zfp24, and Myrf during differentiation and myelination, and interpret them in the context of the regulatory network.

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来源期刊
Developmental Neurobiology
Developmental Neurobiology 生物-发育生物学
CiteScore
6.50
自引率
0.00%
发文量
45
审稿时长
4-8 weeks
期刊介绍: Developmental Neurobiology (previously the Journal of Neurobiology ) publishes original research articles on development, regeneration, repair and plasticity of the nervous system and on the ontogeny of behavior. High quality contributions in these areas are solicited, with an emphasis on experimental as opposed to purely descriptive work. The Journal also will consider manuscripts reporting novel approaches and techniques for the study of the development of the nervous system as well as occasional special issues on topics of significant current interest. We welcome suggestions on possible topics from our readers.
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