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早期神经发生的综合基因组分析揭示了前脑板和 Cajal-Retzius 神经元分化和特化的时间遗传程序。

Integrative genomic analysis of early neurogenesis reveals a temporal genetic program for differentiation and specification of preplate and Cajal-Retzius neurons.

机构信息

Key Laboratory of Spine and Spinal Cord Injury Repair and Regeneration of Ministry of Education, Orthopaedic Department of Tongji Hospital, School of Life Sciences and Technology, Tongji University, Shanghai, China.

PTN graduate program, School of Life Sciences, Peking University, Beijing, China.

出版信息

PLoS Genet. 2021 Mar 24;17(3):e1009355. doi: 10.1371/journal.pgen.1009355. eCollection 2021 Mar.

Abstract

Neurogenesis in the developing neocortex begins with the generation of the preplate, which consists of early-born neurons including Cajal-Retzius (CR) cells and subplate neurons. Here, utilizing the Ebf2-EGFP transgenic mouse in which EGFP initially labels the preplate neurons then persists in CR cells, we reveal the dynamic transcriptome profiles of early neurogenesis and CR cell differentiation. Genome-wide RNA-seq and ChIP-seq analyses at multiple early neurogenic stages have revealed the temporal gene expression dynamics of early neurogenesis and distinct histone modification patterns in early differentiating neurons. We have identified a new set of coding genes and lncRNAs involved in early neuronal differentiation and validated with functional assays in vitro and in vivo. In addition, at E15.5 when Ebf2-EGFP+ cells are mostly CR neurons, single-cell sequencing analysis of purified Ebf2-EGFP+ cells uncovers molecular heterogeneities in CR neurons, but without apparent clustering of cells with distinct regional origins. Along a pseudotemporal trajectory these cells are classified into three different developing states, revealing genetic cascades from early generic neuronal differentiation to late fate specification during the establishment of CR neuron identity and function. Our findings shed light on the molecular mechanisms governing the early differentiation steps during cortical development, especially CR neuron differentiation.

摘要

发育中的新皮层中的神经发生始于前板的产生,前板由包括 Cajal-Retzius (CR) 细胞和基板神经元在内的早期出生的神经元组成。在这里,我们利用 Ebf2-EGFP 转基因小鼠,其中 EGFP 最初标记前板神经元,然后持续存在于 CR 细胞中,揭示了早期神经发生和 CR 细胞分化的动态转录组谱。在多个早期神经发生阶段进行的全基因组 RNA-seq 和 ChIP-seq 分析揭示了早期神经发生的时间基因表达动态和早期分化神经元中独特的组蛋白修饰模式。我们已经确定了一组新的参与早期神经元分化的编码基因和 lncRNA,并通过体外和体内功能测定进行了验证。此外,在 E15.5 时,当 Ebf2-EGFP+细胞主要是 CR 神经元时,纯化的 Ebf2-EGFP+细胞的单细胞测序分析揭示了 CR 神经元中的分子异质性,但没有明显的具有不同区域起源的细胞聚类。沿着伪时间轨迹,这些细胞被分为三种不同的发育状态,揭示了在建立 CR 神经元身份和功能期间,从早期通用神经元分化到晚期命运特化的遗传级联。我们的发现揭示了调控皮质发育过程中早期分化步骤的分子机制,特别是 CR 神经元分化的分子机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1310/7990179/b92933c3b8f6/pgen.1009355.g001.jpg

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