Anderson Nathan, Lai Sen-Lin, Doe Chris Q
bioRxiv. 2025 Sep 8:2025.09.04.674256. doi: 10.1101/2025.09.04.674256.
Understanding how neuronal diversity is generated is a major goal of neuroscience. Here we characterize the first step in generating neuronal diversity in the embryo: spatial transcription factors (STFs) expressed in orthogonal rows and columns of neural progenitors. These factors give spatial identity to neural progenitors (neuroblasts, NBs), and are highly conserved in mammals. Here we investigate the roles of Engrailed (En+; posterior row) and Vnd+ (medial column) in specifying the well-characterized progenitor: neuroblast 7-1 (NB7-1). We show that NB7-1 is located at the intersection of Vnd and En, and we identify NB7-1 using a newly characterized gene, , that we show is specifically expressed in NB7-1 and its progeny, giving us a specific assay for NB7-1 identity. We show that En and Vnd are both required for Fd4 expression, and that Vnd and En co-expression is sufficient to induce ectopic Fd4 expression in other NBs and their lineages. Finally, we show that NBs gradually lose competence to respond to En or Vnd. We conclude that En and Vnd are STFs that act combinatorially to specify the identity of an individual progenitor, NB7-1.
理解神经元多样性是如何产生的是神经科学的一个主要目标。在此,我们描述了胚胎中产生神经元多样性的第一步:在神经祖细胞的正交行和列中表达的空间转录因子(STF)。这些因子赋予神经祖细胞(神经母细胞,NB)空间特性,并且在哺乳动物中高度保守。在此,我们研究了Engrailed(En+;后排)和Vnd+(内侧列)在指定特征明确的祖细胞:神经母细胞7-1(NB7-1)中的作用。我们表明NB7-1位于Vnd和En的交叉点,并且我们使用一个新鉴定的基因 来鉴定NB7-1,我们发现该基因在NB7-1及其后代中特异性表达,这为我们提供了一种鉴定NB7-1特性的特异性检测方法。我们表明En和Vnd对于Fd4表达都是必需的,并且Vnd和En的共表达足以在其他神经母细胞及其谱系中诱导异位Fd4表达。最后,我们表明神经母细胞逐渐丧失对En或Vnd作出反应的能力。我们得出结论,En和Vnd是组合作用以指定单个祖细胞NB7-1特性的空间转录因子。