Department of Biology, University of North Carolina at Charlotte , Charlotte, NC 28223 , USA ; Gastrointestinal Unit, Massachusetts General Hospital , Harvard Medical School, 55 Fruit Street, Boston, MA 02114 , USA.
Biol Open. 2013 Jan 15;2(1):1-9. doi: 10.1242/bio.20122725. Epub 2012 Oct 23.
The abundance of Myc protein must be exquisitely controlled to avoid growth abnormalities caused by too much or too little Myc. An intriguing mode of regulation exists in which Myc protein itself leads to reduction in its abundance. We show here that dMyc binds to the miR-308 locus and increases its expression. Using our gain-of-function approach, we show that an increase in miR-308 causes a destabilization of dMyc mRNA and reduced dMyc protein levels. In vivo knockdown of miR-308 confirmed the regulation of dMyc levels in embryos. This regulatory loop is crucial for maintaining appropriate dMyc levels and normal development. Perturbation of the loop, either by elevated miR-308 or elevated dMyc, caused lethality. Combining elevated levels of both, therefore restoring balance between miR-308 and dMyc levels, resulted in lower apoptotic activity and suppression of lethality. These results reveal a sensitive feedback mechanism that is crucial to prevent the pathologies caused by abnormal levels of dMyc.
Myc 蛋白的丰度必须被精细地控制,以避免因 Myc 过多或过少而导致的生长异常。一种引人注目的调节模式存在,其中 Myc 蛋白本身导致其丰度降低。我们在这里表明,dMyc 与 miR-308 基因座结合并增加其表达。使用我们的功能获得方法,我们表明 miR-308 的增加导致 dMyc mRNA 的不稳定性和 dMyc 蛋白水平降低。体内 miR-308 的敲低证实了胚胎中 dMyc 水平的调节。这个调节环对于维持适当的 dMyc 水平和正常发育至关重要。环路的扰动,无论是通过升高的 miR-308 还是升高的 dMyc,都会导致致死性。因此,两者水平的升高相结合,从而恢复 miR-308 和 dMyc 水平之间的平衡,导致较低的细胞凋亡活性和致死性的抑制。这些结果揭示了一种敏感的反馈机制,对于防止由 dMyc 水平异常引起的病理学至关重要。