Bio-X Institutes, Key Laboratory for the Genetics of Developmental and Neuropsychiatric Disorders, Shanghai Jiao Tong University, Shanghai, People's Republic of China.
FEBS Lett. 2011 Oct 3;585(19):2992-7. doi: 10.1016/j.febslet.2011.08.013. Epub 2011 Aug 26.
MiR-140 is a microRNA specially involved in chondrogenesis and osteoarthritis pathogenesis. However, its transcriptional regulation and target genes in cartilage development are not fully understood. Here we detected that miR-140 was uniquely expressed in chondrocyte and suppressed by Wnt/β-catenin signalling. The miR-140 primary transcript was an intron-retained RNA co-expressed with Wwp2-C isoform, which was directly induced by Sox9 through binding to the intron 10 of Wwp2 gene. Knockdown of miR-140 in limb bud micromass cultures resulted in arrest of chondrogenic proliferation. Sp1, the activator of the cell cycle regulator p15(INK4b), was identified as a target of miR-140 in maintaining the chondrocyte proliferation. Collectively, our findings expand our understanding of the transcriptional regulation and the chondrogenic role of miR-140 in chondrogenesis.
miR-140 是一种专门参与软骨生成和骨关节炎发病机制的 microRNA。然而,其在软骨发育中的转录调控和靶基因尚不完全清楚。在这里,我们检测到 miR-140 特异性表达于软骨细胞中,并受到 Wnt/β-catenin 信号的抑制。miR-140 的初级转录物是一种与 Wwp2-C 同种型共表达的内含子保留 RNA,它通过结合 Wwp2 基因内含子 10 直接被 Sox9 诱导。在肢芽微团培养物中敲低 miR-140 会导致软骨生成性增殖停滞。Sp1,细胞周期调节剂 p15(INK4b)的激活剂,被鉴定为 miR-140 在维持软骨细胞增殖中的靶标。总之,我们的发现扩展了我们对 miR-140 在软骨生成中的转录调控和软骨生成作用的理解。