Whole-embryo Spatial Transcriptomics at Subcellular Resolution from Gastrulation to Organogenesis
Yinan WaniD, Jakob El KholteiiD, Ignatius JenieiD, Mariona Colomer-RoselliD, Jialin LiuiD, Qinghua ZhangiD, Joaquín Navajas AcedoiD, Lucia Y. DuiD, Mireia Codina-TobiasiD, Mengfan WangiD, Wei ZhengiD, Edward Lin, Tzy-Harn Chuang, Oded MayselessiD, Ahilya N. SawhiD, Susan E. MangoiD, Guoqiang YuiD, Bogdan BintuiD, Alexander F. SchieriD
Abstract
Spatiotemporal patterns of gene expression underlie embryogenesis. Despite progress in single-cell genomics, mapping these patterns across whole embryos with comprehensive gene coverage and at high resolution has remained elusive. Here, we introduce a whole-embryo imaging platform using multiplexed error-robust fluorescent in-situ hybridization (weMERFISH). We quantified the expression of 495 genes in whole-mount zebrafish embryos at subcellular resolution. Integration with single-cell multiomics data generated an atlas detailing the expression of 25,872 genes and the accessibility of 294,954 chromatin regions, explorable with an online interface MERFISHEYES (beta version). We found that temporal gene expression aligns with cellular maturation and morphogenetic movements, diverse expression patterns correspond to composites of tissue-specific accessible elements, and changes in gene expression generate sharp boundaries during gastrulation. These results establish a novel approach for whole-organism spatial transcriptomics, provide a comprehensive spatially resolved atlas of gene expression and chromatin accessibility, and reveal the diversity, precision and emergence of embryonic patterns.
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