Tracking the embryonic stem cell transition from ground state pluripotency

Author:

Kalkan Tüzer1,Olova Nelly2,Roode Mila1,Mulas Carla1,Lee Heather J.23,Nett Isabelle1,Marks Hendrik4,Walker Rachael12,Stunnenberg Hendrik G.4,Lilley Kathryn S.56,Nichols Jennifer17,Reik Wolf238,Bertone Paul1,Smith Austin15ORCID

Affiliation:

1. Wellcome Trust-Medical Research Council Cambridge Stem Cell Institute, Cambridge CB2 1QR, UK

2. Babraham Institute, Cambridge CB22 3AT, UK

3. Wellcome Trust Sanger Institute, Hinxton CB10 1SA, UK

4. Radboud University, Faculty of Science, Department of Molecular Biology, Radboud Institute for Molecular Life Sciences (RIMLS), 6500HB, Nijmegen, The Netherlands

5. Department of Biochemistry, University of Cambridge, Cambridge CB2 1GA, UK

6. The Cambridge Centre for Proteomics, Cambridge System Biology Centre, University of Cambridge, Cambridge, CB2 1QR, UK

7. Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge CB2 4BG, UK

8. Centre for Trophoblast Research, University of Cambridge, Cambridge CB2 3EG, UK

Abstract

Mouse embryonic stem (ES) cells are locked into self-renewal by shielding from inductive cues. Release from this ground state in minimal conditions offers a system for delineating developmental progression from naive pluripotency. Here we examined the initial transition process. The ES cell population behaves asynchronously. We therefore exploited a short-half-life Rex1::GFP reporter to isolate cells either side of exit from naive status. Extinction of ES cell identity in single cells is acute. It occurs only after near-complete elimination of naïve pluripotency factors, but precedes appearance of lineage specification markers. Cells newly departed from the ES cell state display features of early post-implantation epiblast and are distinct from primed epiblast. They also exhibit a genome-wide increase in DNA methylation, intermediate between early and late epiblast. These findings are consistent with the proposition that naive cells transition to a distinct formative phase of pluripotency preparatory to lineage priming.

Funder

Medical Research Council

Wellcome Trust

Louis-Jeantet Foundation

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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