4.8 Article

Optimal-Transport Analysis of Single-Cell Gene Expression Identifies Developmental Trajectories in Reprogramming

期刊

CELL
卷 176, 期 4, 页码 928-+

出版社

CELL PRESS
DOI: 10.1016/j.cell.2019.01.006

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资金

  1. Broad Institute
  2. NIH [HD045022, R01 MH104610-15, R01NS088538, R01HD058013]
  3. Helen Hay Whitney Foundation
  4. NIH Pathway to Independence Award [K99HD096049]
  5. Klarman Cell Observatory at Broad Institute
  6. CEGS grant from NIH
  7. CASI from the Burroughs Wellcome Fund
  8. NSF [DMS-1712596, TRIPODS-1740751, IIS-1838071]
  9. ONR [N00014-17-1-2147]
  10. CZI [DAF 2018-182642]
  11. MIT Skoltech Seed Fund

向作者/读者索取更多资源

Understanding the molecular programs that guide differentiation during development is a major challenge. Here, we introduce Waddington-OT, an approach for studying developmental time courses to infer ancestor-descendant fates and model the regulatory programs that underlie them. We apply the method to reconstruct the landscape of reprogramming from 315,000 single-cell RNA sequencing (scRNA-seq) profiles, collected at half-day intervals across 18 days. The results reveal a wider range of developmental programs than previously characterized. Cells gradually adopt either a terminal stromal state or a nnesenchymal-to-epithelial transition state. The latter gives rise to populations related to pluripotent, extra-embryonic, and neural cells, with each harboring multiple finer subpopulations. The analysis predicts transcription factors and paracrine signals that affect fates and experiments validate that the TF Obox6 and the cytokine GDF9 enhance reprogramming efficiency. Our approach sheds light on the process and outcome of reprogramming and provides a framework applicable to diverse temporal processes in biology.

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