Department of Molecular and Cellular Biology, Kennesaw State University, Kennesaw, GA 30144.
Department of Molecular and Cellular Biology, Kennesaw State University, Kennesaw, GA 30144
G3 (Bethesda). 2020 Sep 2;10(9):3071-3085. doi: 10.1534/g3.120.401515.
Identifying the mechanisms behind neuronal fate specification are key to understanding normal neural development in addition to neurodevelopmental disorders such as autism and schizophrenia. cell fate specification is difficult to study in vertebrates. However, the nematode , with its invariant cell lineage and simple nervous system of 302 neurons, is an ideal organism to explore the earliest stages of neural development. We used a comparative transcriptome approach to examine the role of /NeuroD1 in nervous system development and function. This basic helix-loop-helix transcription factor is deeply conserved across phyla and plays a crucial role in cell fate specification in both the vertebrate nervous system and pancreas. We find that controls expression of , a Vax2-like homeobox class transcription factor, in the RME head motorneurons and PVQ tail interneurons. We also show that functions redundantly with the Hox gene /labial in defining the fate of DD1 and DD2 embryonic ventral nerve cord motorneurons. These data highlight the utility of comparative transcriptomes for identifying transcription factor targets and understanding gene regulatory networks.
鉴定神经元命运特化的机制对于理解正常神经发育至关重要,此外还包括自闭症和精神分裂症等神经发育障碍。细胞命运特化在脊椎动物中难以研究。然而,线虫具有不变的细胞谱系和简单的 302 个神经元的神经系统,是探索神经发育最早阶段的理想生物体。我们使用比较转录组学方法研究了 /NeuroD1 在神经系统发育和功能中的作用。这个基本螺旋-环-螺旋转录因子在门之间深度保守,在脊椎动物神经系统和胰腺中对细胞命运特化起着至关重要的作用。我们发现 控制着 RME 头部运动神经元和 PVQ 尾部中间神经元中 的表达,这是一种 Vax2 样同源盒类转录因子。我们还表明 与 Hox 基因 /labial 一起,在确定 DD1 和 DD2 胚胎腹侧神经索运动神经元的命运方面具有冗余功能。这些数据突出了比较转录组学在鉴定转录因子靶标和理解基因调控网络方面的效用。