首页> 外文期刊>Scientific reports. >Transcriptional Regulation of Notch1 Expression by Nkx6.1 in Neural Stem/Progenitor Cells during Ventral Spinal Cord Development
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Transcriptional Regulation of Notch1 Expression by Nkx6.1 in Neural Stem/Progenitor Cells during Ventral Spinal Cord Development

机译:NKX6.1在腹侧脊髓发育期间NKX6.1在神经茎/祖细胞中的转录调节

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Notch1 signaling plays a critical role in maintaining and determining neural stem/progenitor cell (NSPC) fate, yet the transcriptional mechanism controlling Notch1 specific expression in NSPCs remains incomplete. Here, we show transcription factor Nkx6.1 interacts with a cis-element (CR2, an evolutionarily conserved non-coding fragment in the second intron of Notch1 locus) and regulates the expression of Notch1 in ventral NSPCs of the developing spinal cord. We show that the Notch1 expression is modulated by the interaction of Nkx6.1 with a 139?bp enhancer sequence within CR2. Knockdown or overexpression of Nkx6.1 leads to down- or up-regulated Notch1 expression, respectively. In CR2-GFP transgenic mouse, GFP expression was found prominent in the ventricular zone and neural progenitor cells from embryonic day 9.5 to postnatal day 7. GFP+ cells were mainly neural progenitors for interneurons and not for motoneurons or glial cells. Moreover, GFP expression persisted in a subset of ependymal cells in the adult spinal cord, suggesting that CR2 is active in both embryonic and adult NSPCs. Together our data reveal a novel mechanism of Notch1 transcriptional regulation in the ventral spinal cord by Nkx6.1 via its binding with Notch1 enhancer CR2 during embryonic development.
机译:Notch1信号传导在维持和确定神经茎/祖细胞(NSPC)命运中起着关键作用,但控制NSPC中Notch1特异性表达的转录机制仍然不完整。在这里,我们显示转录因子NKX6.1与顺式元素(CR2,在Notch1基因座的第二内含子中的进化上保守的非编码片段中的相互作用,并调节缺口脊髓腹部NSPC中Notch1的表达。我们表明NOTCH1表达通过NKX6.1的相互作用与CR2内的139μl增强子序列进行调节。 NKX6.1的敲低或过表达分别导致下调或上调的Notch1表达。在CR2-GFP转基因小鼠中,在胚胎第9.5天的心室区和神经祖细胞中发现GFP表达突出至后期7. GFP +细胞主要是用于中间核的神经祖细胞,而不是用于运动神经元或胶质细胞。此外,GFP表达持续存在于成年脊髓中的突变细胞子集中,表明CR2在胚胎和成人NSPC中是活性的。我们的数据在一起揭示了NKX6.1在胚胎发育期间通过与NOTCH1增强子CR2结合的NKX6.1在腹侧脊髓中的Notch1转录调节的新机制。

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