Regulation of PI3-kinase/Akt signaling by muscle-enriched microRNA-486

被引:336
作者
Small, Eric M. [1 ]
O'Rourke, Jason R. [1 ]
Moresi, Viviana [1 ]
Sutherland, Lillian B. [1 ]
McAnally, John [1 ]
Gerard, Robert D. [1 ,2 ]
Richardson, James A. [1 ,3 ]
Olson, Eric N. [1 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Mol Biol, Dallas, TX 75390 USA
[2] Univ Texas SW Med Ctr Dallas, Dept Internal Med, Dallas, TX 75390 USA
[3] Univ Texas SW Med Ctr Dallas, Dept Pathol, Dallas, TX 75390 USA
基金
美国国家卫生研究院;
关键词
Akt signaling; microRNA; muscle growth; myocardin related transcription factor-A; cardiomyocyte; SERUM RESPONSE FACTOR; ACTIN DYNAMICS; EXPRESSION; GENE; HYPERTROPHY; PROLIFERATION; ANKYRIN-1; ISOFORM; DISEASE; GROWTH;
D O I
10.1073/pnas.1000300107
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页码:4218 / 4223
页数:6
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