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Embryonic Stem Cells/Induced Pluripotent Stem Cells
miR-290 Cluster Modulates Pluripotency by Repressing Canonical NF-κB Signaling†‡§
Article first published online: 22 MAR 2012
DOI: 10.1002/stem.1033
Copyright © 2012 AlphaMed Press
Additional Information
How to Cite
Lüningschrör, P., Stöcker, B., Kaltschmidt, B. and Kaltschmidt, C. (2012), miR-290 Cluster Modulates Pluripotency by Repressing Canonical NF-κB Signaling. STEM CELLS, 30: 655–664. doi: 10.1002/stem.1033
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Author contributions: P.L.: conception and design, collection and/or assembly of data, data analysis and interpretation, manuscript writing, and final approval of manuscript; B.S.: collection and/or assembly of data, data analysis and interpretation, and final approval of manuscript; B.K.: conception and design, data analysis and interpretation, and final approval of manuscript; C.K.: financial support, conception and design, data analysis and interpretation, manuscript writing, and final approval of manuscript.
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Disclosure of potential conflicts of interest is found at the end of this article.
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First published online in STEM CELLSEXPRESS January 9, 2012.
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Telephone: +495211065625; Fax: +495211065654
Publication History
- Issue published online: 22 MAR 2012
- Article first published online: 22 MAR 2012
- Accepted manuscript online: 9 JAN 2012 02:55PM EST
- Manuscript Accepted: 19 DEC 2011
- Manuscript Received: 15 SEP 2011
Funded by
- University of Bielefeld and Deutsche Forschungsgemeinschaft (DFG)
Keywords:
- NF-κB;
- Epithelial to mesenchymal transition;
- Pluripotency;
- MicroRNA-290 cluster;
- Embryonic stem cells
Abstract
Embryonic stem cell (ESC)-specific microRNAs (miRNAs) play a critical role in the maintenance of pluripotency and self-renewal but the complete network between these miRNAs and their broad range of target genes still remains elusive. Here we demonstrate that miR-290 cluster, the most abundant miRNA family in ESCs, targets the NF-κB subunit p65 (also known as RelA) by repressing its translation. Forced expression of p65 causes loss of pluripotency, promotes differentiation of ESCs, and leads to an epithelial to mesenchymal transition. These data define p65 as a novel target gene of miR-290 cluster and provide new insight into the function of ESC-specific miRNAs. STEM CELLS2012; 30:655–664

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