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A single-cell analysis of the molecular lineage of chordate embryogenesis

机译:脊柱胚胎发生分子谱系的单细胞分析

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Progressive unfolding of gene expression cascades underlies diverse embryonic lineage development. Here, we report a single-cell RNA sequencing analysis of the complete and invariant embryonic cell lineage of the tunicate Ciona savignyi from fertilization to the onset of gastrulation. We reconstructed a developmental landscape of 47 cell types over eight cell cycles in the wild-type embryo and identified eight fate transformations upon fibroblast growth factor (FGF) inhibition. For most FGF-dependent asymmetric cell divisions, the bipotent mother cell displays the gene signature of the default daughter fate. In convergent differentiation of the two notochord lineages, we identified additional gene pathways parallel to the master regulator T / Brachyury . Last, we showed that the defined Ciona cell types can be matched to E6.5-E8.5 stage mouse cell types and display conserved expression of limited number of transcription factors. This study provides a high-resolution single-cell dataset to understand chordate early embryogenesis and cell lineage differentiation.
机译:基因表达级联的渐进式展开是不同的胚胎谱系发展。在这里,我们报告了剧烈癌症雄蕊的完整和不变胚胎细胞谱系的单细胞RNA测序分析,从施肥到腐化开始。我们在野生型胚胎中重建了47个细胞类型的发育景观,并在成纤维细胞生长因子(FGF)抑制时确定了八个命运转化。对于大多数FGF依赖性的不对称细胞部门,Bipotent Mother Cell显示默认女儿命运的基因签名。在两种脊索谱系的收敛分化中,我们确定了与主调节器T / BRACHYURY平行的额外基因途径。最后,我们表明,定义的CiONa细胞类型可以与E6.5-E8.5阶段小鼠细胞类型匹配,并显示有限数量的转录因子的保守表达。本研究提供了高分辨率的单细胞数据集,以了解脊索曲线早期胚胎发生和细胞谱系分化。

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