BGI-Shenzhen, Shenzhen 518083, China; Shenzhen Key Laboratory of Single-Cell Omics, Shenzhen 518083, China.
BGI-Shenzhen, Shenzhen 518083, China; College of Life Sciences, University of Chinese Academy of Sciences, Beijing 100049, China; Shenzhen Key Laboratory of Single-Cell Omics, Shenzhen 518083, China.
Dev Cell. 2022 May 23;57(10):1284-1298.e5. doi: 10.1016/j.devcel.2022.04.009. Epub 2022 May 4.
A major challenge in understanding vertebrate embryogenesis is the lack of topographical transcriptomic information that can help correlate microenvironmental cues within the hierarchy of cell-fate decisions. Here, we employed Stereo-seq to profile 91 zebrafish embryo sections covering six critical time points during the first 24 h of development, obtaining a total of 152,977 spots at a resolution of 10 × 10 × 15 μm (close to cellular size) with spatial coordinates. Meanwhile, we identified spatial modules and co-varying genes for specific tissue organizations. By performing the integrated analysis of the Stereo-seq and scRNA-seq data from each time point, we reconstructed the spatially resolved developmental trajectories of cell-fate transitions and molecular changes during zebrafish embryogenesis. We further investigated the spatial distribution of ligand-receptor pairs and identified potentially important interactions during zebrafish embryo development. Our study constitutes a fundamental reference for further studies aiming to understand vertebrate development.
理解脊椎动物胚胎发生的主要挑战是缺乏能够帮助在细胞命运决策的层次结构中关联微环境线索的拓扑转录组学信息。在这里,我们采用 Stereo-seq 对 91 个斑马鱼胚胎切片进行了分析,这些切片涵盖了发育的前 24 小时内的六个关键时间点,在 10×10×15μm 的分辨率下(接近细胞大小)总共获得了 152977 个点,具有空间坐标。同时,我们确定了特定组织组织的空间模块和共变基因。通过对每个时间点的 Stereo-seq 和 scRNA-seq 数据进行综合分析,我们重建了斑马鱼胚胎发生过程中细胞命运转变和分子变化的空间分辨发育轨迹。我们进一步研究了配体-受体对的空间分布,并鉴定了斑马鱼胚胎发育过程中潜在的重要相互作用。我们的研究为进一步理解脊椎动物发育提供了基本参考。