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神经分化因子1(NeuroD1)重编程染色质和转录因子格局以诱导神经元程序。

NeuroD1 reprograms chromatin and transcription factor landscapes to induce the neuronal program.

作者信息

Pataskar Abhijeet, Jung Johannes, Smialowski Pawel, Noack Florian, Calegari Federico, Straub Tobias, Tiwari Vijay K

机构信息

Institute of Molecular Biology (IMB), Mainz, Germany.

Adolf Butenandt Institute and Center for Integrated Protein Science, Ludwig Maximilian University, Munich, Germany.

出版信息

EMBO J. 2016 Jan 4;35(1):24-45. doi: 10.15252/embj.201591206. Epub 2015 Oct 29.

Abstract

Cell fate specification relies on the action of critical transcription factors that become available at distinct stages of embryonic development. One such factor is NeuroD1, which is essential for eliciting the neuronal development program and possesses the ability to reprogram other cell types into neurons. Given this capacity, it is important to understand its targets and the mechanism underlying neuronal specification. Here, we show that NeuroD1 directly binds regulatory elements of neuronal genes that are developmentally silenced by epigenetic mechanisms. This targeting is sufficient to initiate events that confer transcriptional competence, including reprogramming of transcription factor landscape, conversion of heterochromatin to euchromatin, and increased chromatin accessibility, indicating potential pioneer factor ability of NeuroD1. The transcriptional induction of neuronal fate genes is maintained via epigenetic memory despite a transient NeuroD1 induction during neurogenesis. NeuroD1 also induces genes involved in the epithelial-to-mesenchymal transition, thereby promoting neuronal migration. Our study not only reveals the NeuroD1-dependent gene regulatory program driving neurogenesis but also increases our understanding of how cell fate specification during development involves a concerted action of transcription factors and epigenetic mechanisms.

摘要

细胞命运特化依赖于关键转录因子的作用,这些转录因子在胚胎发育的不同阶段发挥作用。其中一个这样的因子是NeuroD1,它对于启动神经元发育程序至关重要,并且具有将其他细胞类型重编程为神经元的能力。鉴于这种能力,了解其靶点以及神经元特化的潜在机制非常重要。在这里,我们表明NeuroD1直接结合神经元基因的调控元件,这些基因在发育过程中通过表观遗传机制被沉默。这种靶向作用足以启动赋予转录能力的事件,包括转录因子格局的重编程、异染色质向常染色质的转变以及染色质可及性的增加,这表明NeuroD1具有潜在的先驱因子能力。尽管在神经发生过程中NeuroD1是短暂诱导的,但神经元命运基因的转录诱导通过表观遗传记忆得以维持。NeuroD1还诱导参与上皮-间质转化的基因,从而促进神经元迁移。我们的研究不仅揭示了驱动神经发生的NeuroD1依赖性基因调控程序,还增进了我们对发育过程中细胞命运特化如何涉及转录因子和表观遗传机制协同作用的理解。

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