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首页> 外文期刊>Journal of neurobiology >Regulation of FGF10 by POU transcription factor Brn3a in the developing trigeminal ganglion.
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Regulation of FGF10 by POU transcription factor Brn3a in the developing trigeminal ganglion.

机译:在发育中的三叉神经节中,POU转录因子Brn3a对FGF10的调节。

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The POU-domain transcription factor Brn3a is expressed in specific neurons of the caudal CNS and peripheral sensory nervous system. The sensory neurons of mice lacking Brn3a exhibit marked defects in axon growth and extensive apoptosis in late gestation. Here we show that expression of the developmental regulator FGF10 is approximately 35-fold increased in the developing trigeminal ganglia of Brn3a-null mice. In order to determine whether FGF10 regulates other changes in gene expression observed in Brn3a knock-out ganglia, we have used a sensory-specific enhancer to over-express FGF10 in transgenic mice. Microarray analysis of trigeminal ganglia from individual transgenic founders effectively excludes the cell-autonomous activity of FGF10 as a mechanism for mediating the downstream effects of the loss of Brn3a, probably because developing sensory neurons lack the appropriate type of FGF receptor.
机译:POU域转录因子Brn3a在尾部CNS和周围感觉神经系统的特定神经元中表达。缺乏Brn3a的小鼠的感觉神经元在晚期妊娠中显示出明显的轴突生长缺陷和广泛的细胞凋亡。在这里,我们显示在Brn3a-null小鼠的三叉神经节中,发育调控因子FGF10的表达增加了约35倍。为了确定FGF10是否调节在Brn3a敲除神经节中观察到的基因表达的其他变化,我们使用了一种感觉特异性增强子在转基因小鼠中过表达FGF10。来自个别转基因创建者的三叉神经节的微阵列分析有效地排除了FGF10的细胞自主活性,作为介导Brn3a丧失的下游效应的一种机制,这可能是因为发育的感觉神经元缺乏适当类型的FGF受体。

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