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Elevated p53 Activities Restrict Differentiation Potential of MicroRNA-Deficient Pluripotent Stem Cells

Pluripotent stem cells (PSCs) deficient for microRNAs (miRNAs), such as Dgcr8(−/−) or Dicer(−/–) embryonic stem cells (ESCs), contain no mature miRNA and cannot differentiate into somatic cells. How miRNA deficiency causes differentiation defects remains poorly understood. Here, we report that miR-3...

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Detalles Bibliográficos
Autores principales: Liu, Zhong, Zhang, Cheng, Skamagki, Maria, Khodadadi-Jamayran, Alireza, Zhang, Wei, Kong, Dexin, Chang, Chia-Wei, Feng, Jingyang, Han, Xiaosi, Townes, Tim M., Li, Hu, Kim, Kitai, Zhao, Rui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5688240/
https://www.ncbi.nlm.nih.gov/pubmed/29141234
http://dx.doi.org/10.1016/j.stemcr.2017.10.006
Descripción
Sumario:Pluripotent stem cells (PSCs) deficient for microRNAs (miRNAs), such as Dgcr8(−/−) or Dicer(−/–) embryonic stem cells (ESCs), contain no mature miRNA and cannot differentiate into somatic cells. How miRNA deficiency causes differentiation defects remains poorly understood. Here, we report that miR-302 is sufficient to enable neural differentiation of differentiation-incompetent Dgcr8(−/−) ESCs. Our data showed that miR-302 directly suppresses the tumor suppressor p53, which is modestly upregulated in Dgcr8(−/−) ESCs and serves as a barrier restricting neural differentiation. We demonstrated that direct inactivation of p53 by SV40 large T antigen, a short hairpin RNA against Trp53, or genetic ablation of Trp53 in Dgcr8(−/−) PSCs enables neural differentiation, while activation of p53 by the MDM2 inhibitor nutlin-3a in wild-type ESCs inhibits neural differentiation. Together, we demonstrate that a major function of miRNAs in neural differentiation is suppression of p53 and that modest activation of p53 blocks neural differentiation of miRNA-deficient PSCs.