4.8 Article

A single-cell molecular map of mouse gastrulation and early organogenesis

期刊

NATURE
卷 566, 期 7745, 页码 490-+

出版社

NATURE PORTFOLIO
DOI: 10.1038/s41586-019-0933-9

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资金

  1. Wellcome
  2. MRC
  3. CRUK
  4. Bloodwise
  5. NIH-NIDDK
  6. Wellcome-MRC Cambridge Stem Cell Institute
  7. European Molecular Biology Laboratory
  8. Wellcome 4-Year PhD Programme in Stem Cell Biology and Medicine
  9. University of Cambridge
  10. Cambridge Commonwealth European and International Trust
  11. Wellcome Mathematical Genomics and Medicine Programme at the University of Cambridge [109081/Z/15/A]
  12. Swedish Research Council [2017-06278]
  13. Wellcome Strategic Award [105031/Z/14/Z]
  14. Wellcome [108438/Z/15]
  15. BBSRC [BBS/E/B/000C0421]
  16. Swedish Research Council [2017-06278] Funding Source: Swedish Research Council
  17. BBSRC [BBS/E/B/000C0421, BBS/E/B/000C0422, BB/J00989X/1] Funding Source: UKRI
  18. MRC [MR/M008975/1] Funding Source: UKRI
  19. Wellcome Trust [105031/Z/14/Z, 109081/Z/15/A] Funding Source: Wellcome Trust

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Across the animal kingdom, gastrulation represents a key developmental event during which embryonic pluripotent cells diversify into lineage-specific precursors that will generate the adult organism. Here we report the transcriptional profiles of 116,312 single cells from mouse embryos collected at nine sequential time points ranging from 6.5 to 8.5 days post-fertilization. We construct a molecular map of cellular differentiation from pluripotency towards all major embryonic lineages, and explore the complex events involved in the convergence of visceral and primitive streak-derived endoderm. Furthermore, we use single-cell profiling to show that Tal1(-/-) chimeric embryos display defects in early mesoderm diversification, and we thus demonstrate how combining temporal and transcriptional information can illuminate gene function. Together, this comprehensive delineation of mammalian cell differentiation trajectories in vivo represents a baseline for understanding the effects of gene mutations during development, as well as a roadmap for the optimization of in vitro differentiation protocols for regenerative medicine.

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