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解析和建模 TGF-β 信号相互作用,指定海胆胚胎的背腹轴。

Deciphering and modelling the TGF-β signalling interplays specifying the dorsal-ventral axis of the sea urchin embryo.

机构信息

Department of Biology, Institut de Biologie de l'ENS (IBENS), École Normale Supérieure, CNRS, INSERM, Université PSL, 75005 Paris, France.

Institut Biologie Valrose, Université Côte d'Azur, 06108 Nice, France.

出版信息

Development. 2021 Jan 20;148(2):dev189944. doi: 10.1242/dev.189944.

Abstract

During sea urchin development, secretion of Nodal and BMP2/4 ligands and their antagonists Lefty and Chordin from a ventral organiser region specifies the ventral and dorsal territories. This process relies on a complex interplay between the Nodal and BMP pathways through numerous regulatory circuits. To decipher the interplay between these pathways, we used a combination of treatments with recombinant Nodal and BMP2/4 proteins and a computational modelling approach. We assembled a logical model focusing on cell responses to signalling inputs along the dorsal-ventral axis, which was extended to cover ligand diffusion and enable multicellular simulations. Our model simulations accurately recapitulate gene expression in wild-type embryos, accounting for the specification of ventral ectoderm, ciliary band and dorsal ectoderm. Our model simulations further recapitulate various morphant phenotypes, reveal a dominance of the BMP pathway over the Nodal pathway and stress the crucial impact of the rate of Smad activation in dorsal-ventral patterning. These results emphasise the key role of the mutual antagonism between the Nodal and BMP2/4 pathways in driving early dorsal-ventral patterning of the sea urchin embryo.

摘要

在海胆发育过程中,来自腹侧组织者区域的 Nodal 和 BMP2/4 配体及其拮抗剂 Lefty 和 Chordin 的分泌将腹侧和背侧区域指定。这个过程依赖于 Nodal 和 BMP 途径之间的复杂相互作用,通过许多调节回路。为了解析这些途径之间的相互作用,我们使用了重组 Nodal 和 BMP2/4 蛋白的组合处理和计算建模方法。我们组装了一个逻辑模型,重点关注沿背腹轴的信号输入的细胞反应,该模型扩展到包括配体扩散,并能够进行多细胞模拟。我们的模型模拟准确地再现了野生型胚胎中的基因表达,说明了腹侧外胚层、纤毛带和背侧外胚层的指定。我们的模型模拟进一步再现了各种形态发生表型,揭示了 BMP 途径对 Nodal 途径的主导作用,并强调了 Smad 激活速率在背腹模式形成中的关键影响。这些结果强调了 Nodal 和 BMP2/4 途径之间的相互拮抗在驱动海胆胚胎早期背腹模式形成中的关键作用。

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