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MorphoSeq: Full Single-Cell Transcriptome Dynamics Up to Gastrulation in a Chordate.
Sladitschek, Hanna L; Fiuza, Ulla-Maj; Pavlinic, Dinko; Benes, Vladimir; Hufnagel, Lars; Neveu, Pierre A.
Affiliation
  • Sladitschek HL; Cell Biology and Biophysics Unit, European Molecular Biology Laboratory, 69117 Heidelberg, Germany; Department of Molecular Medicine, University of Padua School of Medicine, 35126 Padua, Italy.
  • Fiuza UM; Cell Biology and Biophysics Unit, European Molecular Biology Laboratory, 69117 Heidelberg, Germany.
  • Pavlinic D; Genomics Core Facility, European Molecular Biology Laboratory, 69117 Heidelberg, Germany.
  • Benes V; Genomics Core Facility, European Molecular Biology Laboratory, 69117 Heidelberg, Germany.
  • Hufnagel L; Cell Biology and Biophysics Unit, European Molecular Biology Laboratory, 69117 Heidelberg, Germany. Electronic address: hufnagel@embl.de.
  • Neveu PA; Cell Biology and Biophysics Unit, European Molecular Biology Laboratory, 69117 Heidelberg, Germany. Electronic address: neveu@embl.de.
Cell ; 181(4): 922-935.e21, 2020 05 14.
Article in En | MEDLINE | ID: mdl-32315617
ABSTRACT
Single-cell RNA sequencing (scRNA-seq) provides a leap forward in resolving cellular diversity and developmental trajectories but fails to comprehensively delineate the spatial organization and precise cellular makeup of individual embryos. Here, we reconstruct from scRNA-seq and light sheet imaging data a canonical digital embryo that captures the genome-wide gene expression trajectory of every single cell at every cell division in the 18 lineages up to gastrulation in the ascidian Phallusia mammillata. By using high-coverage scRNA-seq, we devise a computational framework that stratifies single cells of individual embryos into cell types without prior knowledge. Unbiased transcriptome data analysis mapped each cell's physical position and lineage history, yielding the complete history of gene expression at the genome-wide level for every single cell in a developing embryo. A comparison of individual embryos reveals both extensive reproducibility between symmetric embryo sides and a large inter-embryonic variability due to small differences in embryogenesis timing.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sequence Analysis, RNA / Gene Expression Profiling / Single-Cell Analysis Limits: Animals Language: En Journal: Cell Year: 2020 Type: Article Affiliation country: Italy

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sequence Analysis, RNA / Gene Expression Profiling / Single-Cell Analysis Limits: Animals Language: En Journal: Cell Year: 2020 Type: Article Affiliation country: Italy