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      Optimal-transport analysis of single-cell gene expression identifies developmental trajectories in reprogramming

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          Summary

          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 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 mesenchymal-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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          Author and article information

          Journal
          0413066
          2830
          Cell
          Cell
          Cell
          0092-8674
          1097-4172
          1 February 2019
          31 January 2019
          07 February 2019
          07 February 2020
          : 176
          : 4
          : 928-943.e22
          Affiliations
          [1 ]Klarman Cell Observatory, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA
          [2 ]Whitehead Institute for Biomedical Research, Cambridge, MA 02142, USA
          [3 ]Computational and Systems Biology Program, MIT, Cambridge, MA 02142, USA
          [4 ]Harvard-MIT Division of Health Sciences and Technology, Cambridge, MA 02139 USA
          [5 ]Cancer Center, Massachusetts General Hospital, Boston, MA 02114 USA
          [6 ]Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA
          [7 ]Department of Molecular Biology, Center for Regenerative Medicine and Cancer Center, Massachusetts General Hospital, Boston, MA 02114, USA
          [8 ]Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA 02138, USA
          [9 ]Harvard Stem Cell Institute, Cambridge, MA 02138, USA
          [10 ]Harvard Medical School, Boston, MA 02115, USA
          [11 ]MIT Center for Statistics, Massachusetts Institute of Technology, Cambridge, MA 02139, USA
          [12 ]Department of Mathematics, Massachusetts Institute of Technology, Cambridge, MA 02139, USA
          [13 ]Howard Hughes Medical Institute, Chevy Chase, MD, USA
          [14 ]Department of Systems Biology Harvard Medical School, Boston, MA 02125, USA
          [15 ]Biochemistry Program, Wellesley College, Wellesley, 02481, MA, USA
          Author notes
          []Corresponding author.
          [#]

          Lead contact.

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          Present Address: Weizmann Institute of Science, Rehovot, Israel

          Author Contributions:

          JS and ESL conceived and designed the study of reprogramming in single-cell resolution. GS and ESL conceived the application of optimal transport; PR, AR, MT, and BC provided input on the development of the approach. MT, GS, BC, and JG developed WADDINGTON-OT. MT, GS, BC, ESL and A.R. analyzed the data, with assistance from J.S. All experiments were designed and performed by JS, with input from RJ and assistance from AS, SL, SL, PB, LL, JB, KH and VS. The manuscript was written by ESL, AR, GS, BC, MT, JS, and VS.

          Article
          PMC6402800 PMC6402800 6402800 nihpa1519815
          10.1016/j.cell.2019.01.006
          6402800
          30712874
          1047df7d-c9cb-4028-9afb-2f1849a60f98
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