Department of Molecular Biology, University of Texas Southwestern Medical Center, Dallas, TX 75390-9148, USA.
Proc Natl Acad Sci U S A. 2010 Mar 2;107(9):4218-23. doi: 10.1073/pnas.1000300107. Epub 2010 Feb 8.
microRNAs (miRNAs) play key roles in modulating a variety of cellular processes through repression of mRNA targets. In a screen for miRNAs regulated by myocardin-related transcription factor-A (MRTF-A), a coactivator of serum response factor (SRF), we discovered a muscle-enriched miRNA, miR-486, controlled by an alternative promoter within intron 40 of the Ankyrin-1 gene. Transcription of miR-486 is directly controlled by SRF and MRTF-A, as well as by MyoD. Among the most strongly predicted targets of miR-486 are phosphatase and tensin homolog (PTEN) and Foxo1a, which negatively affect phosphoinositide-3-kinase (PI3K)/Akt signaling. Accordingly, PTEN and Foxo1a protein levels are reduced by miR-486 overexpression, which, in turn, enhances PI3K/Akt signaling. Similarly, we show that MRTF-A promotes PI3K/Akt signaling by up-regulating miR-486 expression. Conversely, inhibition of miR-486 expression enhances the expression of PTEN and Foxo1a and dampens signaling through the PI3K/Akt-signaling pathway. Our findings implicate miR-486 as a downstream mediator of the actions of SRF/MRTF-A and MyoD in muscle cells and as a potential modulator of PI3K/Akt signaling.
微小 RNA(miRNAs)通过抑制 mRNA 靶标在调节多种细胞过程中发挥关键作用。在针对肌球蛋白相关转录因子-A(MRTF-A)调节的 miRNA 筛选中,MRTF-A 是血清反应因子(SRF)的共激活因子,我们发现了一种丰富的肌肉 miRNA,miR-486,由 Ankyrin-1 基因内含子 40 中的替代启动子控制。miR-486 的转录受 SRF 和 MRTF-A 以及 MyoD 的直接控制。miR-486 最强烈预测的靶标之一是磷酸酶和张力蛋白同源物(PTEN)和 Foxo1a,它们负向影响磷酸肌醇-3-激酶(PI3K)/Akt 信号通路。相应地,PTEN 和 Foxo1a 蛋白水平因 miR-486 过表达而降低,而 miR-486 过表达又增强了 PI3K/Akt 信号通路。同样,我们表明 MRTF-A 通过上调 miR-486 表达促进 PI3K/Akt 信号通路。相反,抑制 miR-486 表达会增强 PTEN 和 Foxo1a 的表达,并抑制 PI3K/Akt 信号通路的信号转导。我们的研究结果表明,miR-486 是 SRF/MRTF-A 和 MyoD 在肌肉细胞中作用的下游介质,并且是 PI3K/Akt 信号通路的潜在调节剂。