Abstract
MicroRNAs are posttranscriptional regulators of gene expression, but their roles in controlling self-renewal and pluripotency of human embryonic stem cells (hESCs) remain unclear. Our recent study indicates that the level of microRNA-145 (miR-145) is low in hESCs but highly upregulated during differentiation. Endogenous miR-145 is sufficient to repress the 3′ untranslated regions of OCT4, SOX2, and KLF4. By downregulating OCT4 and SOX2, increased miR-145 inhibits hESC self-renewal, represses pluripotency, and induces lineage-restricted differentiation. Furthermore, the miR-145 promoter is bound and repressed by OCT4 in hESCs. Thus, miR-145 plays key roles in repressing hESC pluripotency and promoting differentiation. This work reveals a direct link between the core reprogramming factors and miR-145 and uncovers a double-negative feedback loop involving OCT4, SOX2, KLF4, and miR-145.
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Xu, N., Kosik, K.S. (2011). Function of MicroRNA-145 in Human Embryonic Stem Cell Pluripotency. In: Appasani, K., Appasani, R. (eds) Stem Cells & Regenerative Medicine. Stem Cell Biology and Regenerative Medicine. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-60761-860-7_9
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DOI: https://doi.org/10.1007/978-1-60761-860-7_9
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