miR-290 contributes to the low abundance of cyclin D1 protein in mouse embryonic stem cells

Mouse miR-290 cluster miRNAs are expressed specifically in early embryos and embryonic germ cells. These miRNAs play critical roles in the maintenance of pluripotency and self-renewal. Here, we showed that Cyclin D1 is a direct target gene of miR-290 cluster miRNAs. Negative relationships between th...

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Veröffentlicht in:Acta biochimica et biophysica Sinica 2017-07, Vol.49 (7), p.635-642
Hauptverfasser: Gong, Zizhen, Wang, Detao, Zhu, Shaoliang, Xia, Yuqing, Fan, Chunsun, Zhao, Botao, Jin, Youxin
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Sprache:eng
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Zusammenfassung:Mouse miR-290 cluster miRNAs are expressed specifically in early embryos and embryonic germ cells. These miRNAs play critical roles in the maintenance of pluripotency and self-renewal. Here, we showed that Cyclin D1 is a direct target gene of miR-290 cluster miRNAs. Negative relationships between the expression of Cyclin D1 protein and miR-290 cluster miRNAs in pluripotent and non-pluripotent cells, as well as in differentiating CGR8 cells were observed. Inhibition of miR-290 cluster miRNAs could arrest cells at the G1 phase and slow down the cell proliferation in CGR8 mouse stem cells. Since miR-290 cluster miRNAs are the most dominant stem-cell-specific miRNAs, our results revealed an important cause for the absence of Cyclin D1 in mouse embryonic stem cells.
ISSN:1672-9145
1745-7270
DOI:10.1093/abbs/gmx049