The interferon γ pathway enhances pluripotency and X-chromosome reactivation in iPSC reprogramming

Author:

Barrero Mercedes1ORCID,Lazarenkov Aleksey2ORCID,Blanco Enrique1ORCID,Palma Luis G.23ORCID,López-Rubio Anna V.2ORCID,Bauer Moritz1ORCID,Bigas Anna23ORCID,Di Croce Luciano145ORCID,Sardina José Luis2ORCID,Payer Bernhard14ORCID

Affiliation:

1. Centre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Dr. Aiguader 88, Barcelona 08003, Spain.

2. Josep Carreras Leukemia Research Institute (IJC), Badalona 08916, Spain.

3. Institut Hospital del Mar d’Investigacions Mèdiques, CIBERONC, Barcelona 08003, Spain.

4. Universitat Pompeu Fabra (UPF), Barcelona 08003, Spain.

5. ICREA, Passeig Lluís Companys 23, Barcelona 08010, Spain.

Abstract

Reprogramming somatic cells into induced pluripotent stem cells (iPSCs) requires activation of the pluripotency network and resetting of the epigenome by erasing the epigenetic memory of the somatic state. In female mouse cells, a critical epigenetic reprogramming step is the reactivation of the inactive X chromosome. Despite its importance, a systematic understanding of the regulatory networks linking pluripotency and X-reactivation is missing. Here, we reveal important pathways for pluripotency acquisition and X-reactivation using a genome-wide CRISPR screen during neural precursor to iPSC reprogramming. In particular, we discover that activation of the interferon γ (IFNγ) pathway early during reprogramming accelerates pluripotency acquisition and X-reactivation. IFNγ stimulates STAT3 signaling and the pluripotency network and leads to enhanced TET-mediated DNA demethylation, which consequently boosts X-reactivation. We therefore gain a mechanistic understanding of the role of IFNγ in reprogramming and X-reactivation and provide a comprehensive resource of the molecular networks involved in these processes.

Publisher

American Association for the Advancement of Science (AAAS)

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