Genome-wide screening identifies Polycomb repressive complex 1.3 as an essential regulator of human naïve pluripotent cell reprogramming

Author:

Collier Amanda J.12ORCID,Bendall Adam1ORCID,Fabian Charlene1,Malcolm Andrew A.13ORCID,Tilgner Katarzyna4,Semprich Claudia I.1ORCID,Wojdyla Katarzyna1ORCID,Nisi Paola Serena1,Kishore Kamal5ORCID,Roamio Franklin Valar Nila5,Mirshekar-Syahkal Bahar4ORCID,D’Santos Clive5ORCID,Plath Kathrin2ORCID,Yusa Kosuke46ORCID,Rugg-Gunn Peter J.13ORCID

Affiliation:

1. Epigenetics Programme, Babraham Institute, Cambridge, UK.

2. Department of Biological Chemistry, David Geffen School of Medicine, UCLA, Los Angeles, CA, USA.

3. Wellcome–MRC Cambridge Stem Cell Institute, Jeffrey Cheah Biomedical Centre, University of Cambridge, Cambridge, UK.

4. Stem Cell Genetics, Wellcome Sanger Institute, Hinxton, Cambridge, UK.

5. Cancer Research UK Cambridge Institute, University of Cambridge, Cambridge, UK.

6. Stem Cell Genetics, Institute for Frontier Life and Medical Sciences, Kyoto University, Kyoto, Japan.

Abstract

Uncovering the mechanisms that establish naïve pluripotency in humans is crucial for the future applications of pluripotent stem cells including the production of human blastoids. However, the regulatory pathways that control the establishment of naïve pluripotency by reprogramming are largely unknown. Here, we use genome-wide screening to identify essential regulators as well as major impediments of human primed to naïve pluripotent stem cell reprogramming. We discover that factors essential for cell state change do not typically undergo changes at the level of gene expression but rather are repurposed with new functions. Mechanistically, we establish that the variant Polycomb complex PRC1.3 and PRDM14 jointly repress developmental and gene regulatory factors to ensure naïve cell reprogramming. In addition, small-molecule inhibitors of reprogramming impediments improve naïve cell reprogramming beyond current methods. Collectively, this work defines the principles controlling the establishment of human naïve pluripotency and also provides new insights into mechanisms that destabilize and reconfigure cell identity during cell state transitions.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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