The Francis Crick Institute, London, United Kingdom.
Department of Neurobiology, Eli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research, David Geffen School of Medicine at UCLA, University of California, Los Angeles, Los Angeles, California, United States of America.
PLoS Biol. 2018 Feb 1;16(2):e2003127. doi: 10.1371/journal.pbio.2003127. eCollection 2018 Feb.
During tissue development, multipotent progenitors differentiate into specific cell types in characteristic spatial and temporal patterns. We addressed the mechanism linking progenitor identity and differentiation rate in the neural tube, where motor neuron (MN) progenitors differentiate more rapidly than other progenitors. Using single cell transcriptomics, we defined the transcriptional changes associated with the transition of neural progenitors into MNs. Reconstruction of gene expression dynamics from these data indicate a pivotal role for the MN determinant Olig2 just prior to MN differentiation. Olig2 represses expression of the Notch signaling pathway effectors Hes1 and Hes5. Olig2 repression of Hes5 appears to be direct, via a conserved regulatory element within the Hes5 locus that restricts expression from MN progenitors. These findings reveal a tight coupling between the regulatory networks that control patterning and neuronal differentiation and demonstrate how Olig2 acts as the developmental pacemaker coordinating the spatial and temporal pattern of MN generation.
在组织发育过程中,多能祖细胞按照特定的时空模式分化为特定的细胞类型。我们研究了将祖细胞特性与分化速度联系起来的机制,在神经管中,运动神经元(MN)祖细胞比其他祖细胞分化得更快。我们使用单细胞转录组学来定义与神经祖细胞向 MN 分化相关的转录变化。从这些数据重建基因表达动态表明,MN 决定因素 Olig2 在 MN 分化之前起着关键作用。Olig2 抑制 Notch 信号通路效应物 Hes1 和 Hes5 的表达。Olig2 对 Hes5 的抑制似乎是直接的,通过 Hes5 基因座内的一个保守调控元件,限制了从 MN 祖细胞的表达。这些发现揭示了控制模式形成和神经元分化的调控网络之间的紧密联系,并展示了 Olig2 如何作为发育起搏器,协调 MN 生成的空间和时间模式。