Key Laboratory for Clinical Laboratory Diagnostics of Education Ministry of China, Chongqing Medical University, People's Republic of China.
PLoS One. 2012;7(10):e47914. doi: 10.1371/journal.pone.0047914. Epub 2012 Oct 22.
Bub1 is a critical component of the spindle assembly checkpoint (SAC) and closely linked to cell proliferation and differentiation. We previously found that spontaneous abortion embryos contained a low level of Bub1 protein but normal mRNA level, while the knockdown of Bub1 leads to abnormal numerical chromosomes in embryonic cells. Here, we investigated the mechanism through which governs the post-transcriptional regulation of Bub1 protein expression level. We first conducted bioinformatics analysis and identified eight putative miRNAs that may target Bub1. Luciferase reporter assay confirmed that miR-450a-3p can directly regulate Bub1 by binding to the 3'-untranslated region of Bub1 mRNA. We found that the overexpression of miR-450a-3p in mouse embryonic fibroblast (MEF) cells down-regulated Bub1 protein level, repressed cell proliferation, increased apoptosis and restricted most cells in G1 phase of the cell cycle. Furthermore, when the fertilized eggs were microinjected with miR-450a-3p mimics, the cleavage of zygotes was effectively suppressed. Our results strongly suggest that an abnormally decreased Bub1 level regulated by miRNAs may be implicated in the pathogenesis of spontaneous miscarriage. Therefore, the blockade of miR-450a-3p may be explored as a novel therapeutic strategy for preventing spontaneous miscarriages.
Bub1 是纺锤体组装检查点 (SAC) 的关键组成部分,与细胞增殖和分化密切相关。我们之前发现,自发流产胚胎中 Bub1 蛋白水平较低,但 mRNA 水平正常,而 Bub1 的敲低导致胚胎细胞的染色体数目异常。在这里,我们研究了调节 Bub1 蛋白表达水平的转录后调控机制。我们首先进行了生物信息学分析,鉴定出了 8 个可能靶向 Bub1 的假定 miRNA。荧光素酶报告基因实验证实,miR-450a-3p 可以通过结合 Bub1 mRNA 的 3'非翻译区直接调控 Bub1。我们发现,在小鼠胚胎成纤维细胞 (MEF) 细胞中过表达 miR-450a-3p 可下调 Bub1 蛋白水平,抑制细胞增殖,增加细胞凋亡,并将大多数细胞阻滞在细胞周期的 G1 期。此外,当用 miR-450a-3p 模拟物微注射受精卵时,有效地抑制了胚胎的卵裂。我们的结果强烈表明,miRNA 调节的 Bub1 水平异常降低可能与自然流产的发病机制有关。因此,阻断 miR-450a-3p 可能被探索为预防自然流产的一种新的治疗策略。