Wnt/β-catenin signaling pathway safeguards epigenetic stability and homeostasis of mouse embryonic stem cells

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作者
Ilda Theka
Francesco Sottile
Marco Cammisa
Sarah Bonnin
Marta Sanchez-Delgado
Umberto Di Vicino
Maria Victoria Neguembor
Karthik Arumugam
Francesco Aulicino
David Monk
Andrea Riccio
Maria Pia Cosma
机构
[1] The Barcelona Institute of Science and Technology,Centre for Genomic Regulation (CRG)
[2] Institute of Genetics and Biophysics ‘A. Buzzati-Traverso’,Imprinting and Cancer Group, Cancer Epigenetic and Biology Program, Institut d’Investigació Biomedica de Bellvitge
[3] CNR,Universitat Pompeu Fabra
[4] Department of Environmental,undefined
[5] Biological and Pharmaceutical Sciences and Technologies,undefined
[6] Second University of Naples,undefined
[7] Hospital Duran i Reynals,undefined
[8] (UPF),undefined
[9] Institució Catalana de Recerca i Estudis Avançat (ICREA),undefined
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摘要
Mouse embryonic stem cells (mESCs) are pluripotent and can differentiate into cells belonging to the three germ layers of the embryo. However, mESC pluripotency and genome stability can be compromised in prolonged in vitro culture conditions. Several factors control mESC pluripotency, including Wnt/β-catenin signaling pathway, which is essential for mESC differentiation and proliferation. Here we show that the activity of the Wnt/β-catenin signaling pathway safeguards normal DNA methylation of mESCs. The activity of the pathway is progressively silenced during passages in culture and this results into a loss of the DNA methylation at many imprinting control regions (ICRs), loss of recruitment of chromatin repressors, and activation of retrotransposons, resulting into impaired mESC differentiation. Accordingly, sustained Wnt/β-catenin signaling maintains normal ICR methylation and mESC homeostasis and is a key regulator of genome stability.
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