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Regulatory factor X transcription factors control musashi1 transcription in mouse neural stem/progenitor cells

机译:调节因子X转录因子控制小鼠神经干/祖细胞中musashi1的转录

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The transcriptional regulation of neural stem/progenitor cells (NS/PCs) is of great interest in neural development and stem cell biology. The RNA-binding protein Musashi1 (Msi1), which is often employed as a marker for NS/PCs, regulates Notch signaling to maintain NS/PCs in undifferentiated states by the translational repression of Numb expression. Considering these critical roles of Msi1 in the maintenance of NS/PCs, it is extremely important to elucidate the regulatory mechanisms by which Msi1 is selectively expressed in these cells. However, the mechanism regulating Msi1 transcription is unclear. We previously reported that the transcriptional regulatory region of Msi1 is located in the sixth intron of the Msi1 locus in NS/PCs, based on in vitro experiments. In the present study, we generated reporter transgenic mice for the sixth intronic Msi1 enhancer (Msi1-6IE), which show the reporter expression corresponding with endogenous Msi1-positive cells in developing and adult NS/PCs. We found that the core element responsible for this reporter gene activity includes palindromic Regulatory factor X (Rfx) binding sites and that Msi1-6IE was activated by Rfx. Rfx4, which was highly expressed in NS/PCs positive for the Msi1-6IE reporter, bound to this region, and both of the palindromic Rfx binding sites were required for the transactivation of Msi1-6IE. Furthermore, ectopic Rfx4 expression in the developing mouse cerebral cortex transactivates Msi1 expression in the intermediate zone. This study suggests that ciliogenic Rfx transcription factors regulate Msi1 expression through Msi1-6IE in NS/PCs.
机译:神经干/祖细胞(NS / PCs)的转录调控在神经发育和干细胞生物学中引起了极大的兴趣。 RNA结合蛋白Musashi1(Msi1)通常被用作NS / PC的标记,通过Numb表达的翻译抑制来调节Notch信号,从而将NS / PC保持在未分化状态。考虑到Msi1在维持NS / PC中的这些关键作用,阐明在这些细胞中选择性表达Msi1的调控机制极为重要。但是,调节Msi1转录的机制尚不清楚。我们以前曾报道,基于体外实验,Msi1的转录调控区位于NS / PCs中Msi1基因座的第六个内含子。在本研究中,我们为第六个内含子Msi1增强子(Msi1-6IE)生成了报告基因转基因小鼠,显示出与发育中和成年NS / PCs中内源性Msi1阳性细胞相对应的报告基因表达。我们发现负责此报告基因活性的核心元素包括回文调节因子X(Rfx)结合位点,并且Msi1-6IE被Rfx激活。 Rfx4(在Msi1-6IE报告基因阳性的NS / PC中高度表达)与该区域结合,并且两个回文的Rfx结合位点都是Msi1-6IE反式激活所必需的。此外,在发育中的小鼠大脑皮层中的异位Rfx4表达激活中间区域Msi1表达。这项研究表明,致龋性Rfx转录因子通过NS / PC中的Msi1-6IE调节Msi1表达。

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