Copley Richard R, Buttin Julia, Arguel Marie-Jeanne, Williaume Géraldine, Lebrigand Kevin, Barbry Pascal, Hudson Clare, Yasuo Hitoyoshi
Laboratoire de Biologie du Développement de Villefranche-sur-mer, Institut de la Mer de Villefranche-sur-mer, Sorbonne Université, CNRS UMR7009, 06230, Villefranche-sur-mer, France.
Laboratoire de Biologie du Développement de Villefranche-sur-mer, Institut de la Mer de Villefranche-sur-mer, Sorbonne Université, CNRS UMR7009, 06230, Villefranche-sur-mer, France.
Dev Biol. 2024 Oct;514:1-11. doi: 10.1016/j.ydbio.2024.06.005. Epub 2024 Jun 13.
In chordates, the central nervous system arises from precursors that have distinct developmental and transcriptional trajectories. Anterior nervous systems are ontogenically associated with ectodermal lineages while posterior nervous systems are associated with mesoderm. Taking advantage of the well-documented cell lineage of ascidian embryos, we asked to what extent the transcriptional states of the different neural lineages become similar during the course of progressive lineage restriction. We performed single-cell RNA sequencing (scRNA-seq) analyses on hand-dissected neural precursor cells of the two distinct lineages, together with those of their sister cell lineages, with a high temporal resolution covering five successive cell cycles from the 16-cell to neural plate stages. A transcription factor binding site enrichment analysis of neural specific genes at the neural plate stage revealed limited evidence for shared transcriptional control between the two neural lineages, consistent with their different ontogenies. Nevertheless, PCA analysis and hierarchical clustering showed that, by neural plate stages, the two neural lineages cluster together. Consistent with this, we identified a set of genes enriched in both neural lineages at the neural plate stage, including miR-124, Celf3.a, Zic.r-b, and Ets1/2. Altogether, the current study has revealed genome-wide transcriptional dynamics of neural progenitor cells of two distinct developmental origins. Our scRNA-seq dataset is unique and provides a valuable resource for future analyses, enabling a precise temporal resolution of cell types not previously described from dissociated embryos.
在脊索动物中,中枢神经系统起源于具有不同发育和转录轨迹的前体细胞。前部神经系统在个体发育上与外胚层谱系相关,而后部神经系统则与中胚层相关。利用海鞘胚胎中记录详尽的细胞谱系,我们探究了在渐进性谱系限制过程中,不同神经谱系的转录状态在多大程度上变得相似。我们对手工解剖的两个不同谱系的神经前体细胞及其姐妹细胞谱系进行了单细胞RNA测序(scRNA-seq)分析,时间分辨率高,涵盖了从16细胞期到神经板期的五个连续细胞周期。对神经板期神经特异性基因的转录因子结合位点富集分析显示,两个神经谱系之间共享转录控制的证据有限,这与其不同的个体发育情况一致。然而,主成分分析和层次聚类表明,到神经板期时,这两个神经谱系聚集在一起。与此一致的是,我们在神经板期鉴定出一组在两个神经谱系中均富集的基因,包括miR-124、Celf3.a、Zic.r-b和Ets1/2。总之,当前研究揭示了两个不同发育起源的神经祖细胞的全基因组转录动态。我们的scRNA-seq数据集独一无二,为未来分析提供了宝贵资源,能够精确解析解离胚胎中以前未描述的细胞类型的时间分辨率。