重编程
诱导多能干细胞
生物
体细胞
表观遗传学
表观基因组
DNA去甲基化
细胞生物学
DNA甲基化
胚胎干细胞
遗传学
细胞
基因
基因表达
作者
Mercedes Barrero,Aleksey Lazarenkov,Enrique Blanco,Luis Galán Palma,Anna Vanessa Lopez-Rubio,Moritz Bauer,Anna Bigas,Luciano Di Croce,José Luis Sardina,Bernhard Payer
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2024-08-09
卷期号:10 (32)
标识
DOI:10.1126/sciadv.adj8862
摘要
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.
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