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The activity of Pax3 and Zic1 regulates three distinct cell fates at the neural plate border

机译:Pax3和Zic1的活性调节神经板边界的三个不同的细胞命运

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In Xenopus, the neural plate border gives rise to at least three cell populations: the neural crest, the preplacodal ectoderm, and the hatching gland. To understand the molecular mechanisms that regulate the formation of these lineages, we have analyzed the role of two transcription factors, Pax3 and Zic1, which are among the earliest genes activated in response to neural plate border-inducing signals. At the end of gastrulation, Pax3 and Zic1 are coexpressed in the neural crest forming region. In addition, Pax3 is expressed in progenitors of the hatching gland, and Zic1 is detected in the preplacodal ectoderm. Using gain of function and knockdown approaches in whole embryos and animal explants, we demonstrate that Pax3 and Zic1 are necessary and sufficient to promote hatching gland and preplacodal fates, respectively, whereas their combined activity is essential to specify the neural crest. Moreover, we show that by manipulating the levels of Pax3 and Zic1 it is possible to shift fates among these cells. These findings provide novel information on the mechanisms regulating cell fate decisions at the neural plate border.
机译:在非洲爪蟾中,神经板边界至少会引起三个细胞种群:神经rest,前斑外胚层和孵化腺。为了了解调节这些谱系形成的分子机制,我们分析了两个转录因子Pax3和Zic1的作用,它们是响应神经板边界诱导信号而被激活的最早基因。在胃形成结束时,Pax3和Zic1在神经neural形成区域共表达。此外,Pax3在孵化腺的祖细胞中表达,而Zic1在斑前外胚层中检测到。使用功能获得和击倒方法在整个胚胎和动物外植体中,我们证明Pax3和Zic1分别是促进孵化腺和前剥离命运的必要和充分条件,而它们的结合活性对于指定神经c至关重要。此外,我们表明通过操纵Pax3和Zic1的水平,可以在这些细胞之间转移命运。这些发现为调节神经板边界细胞命运决定的机制提供了新颖的信息。

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