| Literature DB >> 30712874 |
Geoffrey Schiebinger1, Jian Shu2, Marcin Tabaka3, Brian Cleary4, Vidya Subramanian3, Aryeh Solomon3, Joshua Gould3, Siyan Liu5, Stacie Lin6, Peter Berube3, Lia Lee3, Jenny Chen7, Justin Brumbaugh8, Philippe Rigollet9, Konrad Hochedlinger10, Rudolf Jaenisch11, Aviv Regev12, Eric S Lander13.
Abstract
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 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.Entities:
Keywords: ancestors; descendants; development; iPSCs; optimal-transport; paracrine interactions; regulation; reprogramming; scRNA-seq; trajectories
Mesh:
Substances:
Year: 2019 PMID: 30712874 PMCID: PMC6402800 DOI: 10.1016/j.cell.2019.01.006
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582