Department of Biology, New York University, New York, NY 10003, USA.
Center for Genomics and Systems Biology, New York University Abu Dhabi, Abu Dhabi, United Arab Emirates.
Science. 2018 Oct 12;362(6411):176-180. doi: 10.1126/science.aas9435.
To understand how neurons assemble to form functional circuits, it is necessary to obtain a detailed knowledge of their diversity and to define the developmental specification programs that give rise to this diversity. Invertebrates and vertebrates appear to share common developmental principles of neuronal specification in which cascades of transcription factors temporally pattern progenitors, while spatial cues modify the outcomes of this temporal patterning. Here, we highlight these conserved mechanisms and describe how they are used in distinct neural structures. We present the questions that remain for a better understanding of neuronal specification. Single-cell RNA profiling approaches will potentially shed light on these questions, allowing not only the characterization of neuronal diversity in adult brains, but also the investigation of the developmental trajectories leading to the generation and maintenance of this diversity.
为了了解神经元如何组装形成功能性回路,有必要详细了解它们的多样性,并确定产生这种多样性的发育规范程序。无脊椎动物和脊椎动物似乎都有共同的神经元特化的发育原则,其中转录因子级联在时间上对祖细胞进行模式化,而空间线索则改变这种时间模式化的结果。在这里,我们强调这些保守的机制,并描述它们如何在不同的神经结构中使用。我们提出了仍需解决的问题,以更好地理解神经元特化。单细胞 RNA 分析方法可能会为这些问题提供线索,不仅可以对成年大脑中的神经元多样性进行特征描述,还可以研究导致产生和维持这种多样性的发育轨迹。