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The transcription factor snail regulates osteogenic differentiation by repressing Runx2 expression.

机译:转录因子蜗牛通过抑制Runx2表达来调节成骨分化。

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Osteoblasts originate from mesenchymal stem cells by the coordinated activities of different signaling pathways that regulate the expression of osteoblast-specific genes. Runt-related transcription factor 2 (Runx2) is the master transcription factor for osteoblast differentiation. Despite the importance of Runx2 in the developing skeleton, how Runx2 expression is regulated remains a pivotal question. Snail, a zinc finger transcription factor, is essential for triggering epithelial-to-mesenchymal transitions (EMTs) during embryonic development and tumor progression. Here, we report that Runx2 expression is significantly up- or down-regulated relative to Snail expression. We demonstrate that Snail binds to the Runx2 promoter and that repression of Runx2 transcription by Snail is dependent on specific E-box sequence within the promoter. With antisense morpholino oligonucleotide (MO)-mediated knockdown of Snail expression in zebrafish, we observed alterations in osteogenic potential. These results indicate that Snail plays a crucial role in osteogenic differentiation by acting as a direct Runx2 repressor.
机译:成骨细胞通过调节成骨细胞特异性基因表达的不同信号通路的协调活动而起源于间充质干细胞。矮子相关转录因子2(Runx2)是成骨细胞分化的主要转录因子。尽管Runx2在发育中的骨架中很重要,但是如何调节Runx2的表达仍然是一个关键问题。蜗牛是锌指转录因子,对于在胚胎发育和肿瘤进展过程中触发上皮到间质转化(EMT)至关重要。在这里,我们报告Runx2表达相对于Snail表达明显上调或下调。我们证明Snail绑定到Runx2启动子,并且Snail抑制Runx2转录取决于启动子内的特定E-box序列。用反义吗啉代寡核苷酸(MO)介导的斑马鱼中Snail表达的敲低,我们观察到成骨潜能的变化。这些结果表明,Snail通过直接充当Runx2阻遏物,在成骨分化中起关键作用。

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