| Literature DB >> 23843298 |
Haggai Kaspi1, Elik Chapnik, Maayan Levy, Gilad Beck, Eran Hornstein, Yoav Soen.
Abstract
microRNAs of the miR-290-295 family are selectively expressed at high levels in mouse embryonic stem cells (mESCs) and have established roles in regulating self-renewal. However, the potential influence of these microRNAs on cell fate acquisition during differentiation has been overlooked. Here, we show that miR-290-295 regulate the propensity of mESCs to acquire specific fates. We generated a new miR-290-295-null mESC model, which exhibits increased propensity to generate ectoderm, at the expense of endoderm and mesoderm lineages. We further found that in wild-type cells, miR-290-295 repress Pax6 and ectoderm differentiation; accordingly, Pax6 knockdown partially rescues the mESCs differentiation impairment that is caused by loss of miR-290-295. Thus, in addition to regulating self-renewal, the large reservoir of miR-290-295 in undifferentiated mESCs fine-tunes the expression of master transcriptional factors, such as Pax6, thereby regulating the equilibrium of fate acquisition by mESC descendants. © AlphaMed Press.Entities:
Keywords: Differentiation; Ectoderm; Embryonic Stem Cells; Mesndoderm; Pax6; miR-290-295; miRNA
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Year: 2013 PMID: 23843298 DOI: 10.1002/stem.1465
Source DB: PubMed Journal: Stem Cells ISSN: 1066-5099 Impact factor: 6.277