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BMP 信号通过抑制眼的身份及其 Cxcr4 依赖性形态发生来保护端脑命运。

BMP signaling protects telencephalic fate by repressing eye identity and its Cxcr4-dependent morphogenesis.

机构信息

Medical Research Council Centre for Developmental Neurobiology, King's College London, London SE1 1UL, UK.

出版信息

Dev Cell. 2012 Oct 16;23(4):812-22. doi: 10.1016/j.devcel.2012.09.006.

Abstract

Depletion of Wnt signaling is a major requirement for the induction of the anterior prosencephalon. However, the molecular events driving the differential regionalization of this area into eye-field and telencephalon fates are still unknown. Here we show that the BMP pathway is active in the anterior neural ectoderm during late blastula to early gastrula stage in zebrafish. Bmp2b mutants and mosaic loss-of-function experiments reveal that BMP acts as a repressor of eye-field fate through inhibition of its key transcription factor Rx3, thereby protecting the future telencephalon from acquiring eye identity. This BMP-driven mechanism initiates the establishment of the telencephalon prior to the involvement of Wnt antagonists from the anterior neural border. Furthermore, we demonstrate that Rx3 and BMP are respectively required to maintain and restrict the chemokine receptor cxcr4a, which in turn contributes to the morphogenetic separation of eye-field and telencephalic cells during early neurulation.

摘要

Wnt 信号的耗竭是诱导前脑前脑的主要要求。然而,驱动该区域向眼区和端脑命运进行差异区域化的分子事件仍然未知。在这里,我们显示在斑马鱼的晚期囊胚到早期原肠胚阶段,BMP 途径在前神经外胚层中活跃。Bmp2b 突变体和镶嵌性功能丧失实验表明,BMP 通过抑制其关键转录因子 Rx3 作为眼区命运的抑制剂起作用,从而防止未来的端脑获得眼睛身份。在 Wnt 拮抗剂从前神经边界介入之前,这种 BMP 驱动的机制启动了端脑的建立。此外,我们证明 Rx3 和 BMP 分别需要维持和限制趋化因子受体 cxcr4a,这反过来有助于早期神经胚形成期间眼区和端脑细胞的形态发生分离。

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