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Molecular recording of mammalian embryogenesis.
Chan, Michelle M; Smith, Zachary D; Grosswendt, Stefanie; Kretzmer, Helene; Norman, Thomas M; Adamson, Britt; Jost, Marco; Quinn, Jeffrey J; Yang, Dian; Jones, Matthew G; Khodaverdian, Alex; Yosef, Nir; Meissner, Alexander; Weissman, Jonathan S.
Affiliation
  • Chan MM; Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA, USA.
  • Smith ZD; Howard Hughes Medical Institute, University of California, San Francisco, San Francisco, CA, USA.
  • Grosswendt S; Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Kretzmer H; Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, USA.
  • Norman TM; Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA, USA.
  • Adamson B; Department of Genome Regulation, Max Planck Institute for Molecular Genetics, Berlin, Germany.
  • Jost M; Department of Genome Regulation, Max Planck Institute for Molecular Genetics, Berlin, Germany.
  • Quinn JJ; Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA, USA.
  • Yang D; Howard Hughes Medical Institute, University of California, San Francisco, San Francisco, CA, USA.
  • Jones MG; Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA, USA.
  • Khodaverdian A; Howard Hughes Medical Institute, University of California, San Francisco, San Francisco, CA, USA.
  • Yosef N; Department of Molecular Biology, Lewis Sigler Institute, Princeton University, Princeton, NJ, USA.
  • Meissner A; Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA, USA.
  • Weissman JS; Howard Hughes Medical Institute, University of California, San Francisco, San Francisco, CA, USA.
Nature ; 570(7759): 77-82, 2019 06.
Article in En | MEDLINE | ID: mdl-31086336
Ontogeny describes the emergence of complex multicellular organisms from single totipotent cells. This field is particularly challenging in mammals, owing to the indeterminate relationship between self-renewal and differentiation, variation in progenitor field sizes, and internal gestation in these animals. Here we present a flexible, high-information, multi-channel molecular recorder with a single-cell readout and apply it as an evolving lineage tracer to assemble mouse cell-fate maps from fertilization through gastrulation. By combining lineage information with single-cell RNA sequencing profiles, we recapitulate canonical developmental relationships between different tissue types and reveal the nearly complete transcriptional convergence of endodermal cells of extra-embryonic and embryonic origins. Finally, we apply our cell-fate maps to estimate the number of embryonic progenitor cells and their degree of asymmetric partitioning during specification. Our approach enables massively parallel, high-resolution recording of lineage and other information in mammalian systems, which will facilitate the construction of a quantitative framework for understanding developmental processes.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Embryonic Development / Embryo, Mammalian Limits: Animals Language: En Journal: Nature Year: 2019 Document type: Article Affiliation country: United States Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Embryonic Development / Embryo, Mammalian Limits: Animals Language: En Journal: Nature Year: 2019 Document type: Article Affiliation country: United States Country of publication: United kingdom