Department of Neurosciences, University of New Mexico School of Medicine, Albuquerque, New Mexico, United States of America.
PLoS One. 2013;8(1):e51436. doi: 10.1371/journal.pone.0051436. Epub 2013 Jan 17.
Epigenetic mechanisms, including DNA methylation, histone modification, and microRNAs, play pivotal roles in stem cell biology. Methyl-CpG binding protein 1 (MBD1), an important epigenetic regulator of adult neurogenesis, controls the proliferation and differentiation of adult neural stem/progenitor cells (aNSCs). We recently demonstrated that MBD1 deficiency in aNSCs leads to altered expression of several noncoding microRNAs (miRNAs).
METHODOLOGY/PRINCIPAL FINDINGS: Here we show that one of these miRNAs, miR-195, and MBD1 form a negative feedback loop. While MBD1 directly represses the expression of miR-195 in aNSCs, high levels of miR-195 in turn repress the expression of MBD1. Both gain-of-function and loss-of-function investigations show that alterations of the MBD1-miR-195 feedback loop tip the balance between aNSC proliferation and differentiation.
CONCLUSIONS/SIGNIFICANCE: Therefore the regulatory loop formed by MBD1 and miR-195 is an important component of the epigenetic network that controls aNSC fate.
表观遗传机制,包括 DNA 甲基化、组蛋白修饰和 microRNAs,在干细胞生物学中发挥着关键作用。甲基化CpG 结合蛋白 1(MBD1)是成人神经发生的重要表观遗传调节剂,控制成年神经干细胞/祖细胞(aNSC)的增殖和分化。我们最近的研究表明,aNSC 中的 MBD1 缺乏会导致几种非编码 microRNAs(miRNAs)的表达发生改变。
方法/主要发现:在这里,我们展示了这些 miRNAs 中的一种,miR-195,与 MBD1 形成负反馈回路。虽然 MBD1 直接抑制 aNSC 中 miR-195 的表达,但 miR-195 的高表达反过来又抑制 MBD1 的表达。功能获得和功能丧失的研究表明,MBD1-miR-195 反馈回路的改变会影响 aNSC 的增殖和分化之间的平衡。
结论/意义:因此,MBD1 和 miR-195 形成的调节环是控制 aNSC 命运的表观遗传网络的重要组成部分。