斑马鱼
生物
转录组
命运图
计算生物学
发育生物学
胚胎
胚胎发生
细胞命运测定
脊椎动物
进化生物学
基因
基因表达谱
基因表达
细胞生物学
遗传学
胚胎干细胞
转录因子
作者
Chang Liu,Rui Li,Young Li,Xiumei Lin,Kaichen Zhao,Qun Liu,Shuowen Wang,Xueqian Yang,Xuyang Shi,Yuting Ma,Chenyu Pei,Hui Wang,Wendai Bao,Junhou Hui,Tao Yang,Zhicheng Xu,Tingting Lai,Michael A. Berberoglu,Sunil Kumar Sahu,Miguel A. Esteban
标识
DOI:10.1016/j.devcel.2022.04.009
摘要
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 μm3 (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.
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