a The State Key Laboratory for Agrobiotechnology, College of Biological Sciences, China Agricultural University , Beijing , China.
Cell Cycle. 2017 Sep 17;16(18):1661-1672. doi: 10.1080/15384101.2017.1281479. Epub 2017 Jan 26.
miRNAs are increasingly being implicated as key regulators of cell proliferation, apoptosis, and differentiation. miRNA-34c appears to play a crucial role in cancer pathogenesis wherein it exerts its effect as a tumor suppressor. However, the role of miR-34c in myoblast proliferation remains poorly understood. Here, we found that overexpression miR-34c inhibited myoblasts proliferation by reducing the protein and mRNA expression of cell cycle genes. In contrast, blocking the function of miR-34c promoted myoblasts proliferation and increased the protein and mRNA expression of cell cycle genes. Moreover, miR-34c directly targeted YY1 and inhibited its expression. Similar to overexpression miR-34c, knockdown of YY1 by siRNA suppressed myoblasts proliferation. Our study provides novel evidence for a role of miR-34c in inhibiting myoblasts proliferation by repressing YY1. Thus, miR-34c has the potential to be used to enhance skeletal muscle development and regeneration.
miRNAs 越来越被认为是细胞增殖、凋亡和分化的关键调节因子。miR-34c 似乎在癌症发病机制中发挥着重要作用,作为一种肿瘤抑制因子发挥作用。然而,miR-34c 在成肌细胞增殖中的作用仍知之甚少。在这里,我们发现过表达 miR-34c 通过降低细胞周期基因的蛋白和 mRNA 表达来抑制成肌细胞增殖。相比之下,阻断 miR-34c 的功能促进了成肌细胞增殖,并增加了细胞周期基因的蛋白和 mRNA 表达。此外,miR-34c 可以直接靶向 YY1 并抑制其表达。与过表达 miR-34c 相似,用 siRNA 敲低 YY1 抑制了成肌细胞的增殖。我们的研究为 miR-34c 通过抑制 YY1 抑制成肌细胞增殖提供了新的证据。因此,miR-34c 有可能被用于增强骨骼肌的发育和再生。