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A Boolean Function for Neural Induction Reveals a Critical Role of Direct Intercellular Interactions in Patterning the Ectoderm of the Ascidian Embryo

机译:用于神经感应的布尔函数揭示了直肠间间相互作用在图案化嵌入式胚胎的外胚层中的关键作用

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A complex system of multiple signaling molecules often produce differential gene expression patterns in animal embryos. In the ascidian embryo, four signaling ligands, Ephrin-A.d (Efna.d), Fgf9/16/20, Admp, and Gdf1/3-r, coordinately induce Otx expression in the neural lineage at the 32-cell stage. However, it has not been determined whether differential inputs of all of these signaling pathways are really necessary. It is possible that differential activation of one of these signaling pathways is sufficient and the remaining signaling pathways are activated in all cells at similar levels. To address this question, we developed a parameter-free method for determining a Boolean function for Otx expression in the present study. We treated activities of signaling pathways as Boolean values, and we also took all possible patterns of signaling gradients into consideration. We successfully determined a Boolean function that explains Otx expression in the animal hemisphere of wild-type and morphant embryos at the 32-cell stage. This Boolean function was not inconsistent with three sensing patterns, which represented whether or not individual cells received sufficient amounts of the signaling molecules. These sensing patterns all indicated that differential expression of Otx in the neural lineage is primarily determined by Efna.d, but not by differential inputs of Fgf9/16/20, Admp, and Gdf1/3-r signaling. To confirm this hypothesis experimentally, we simultaneously knocked-down Admp, Gdf1/3-r, and Fgf9/16/20, and treated this triple morphant with recombinant bFGF and BMP4 proteins, which mimic Fgf9/16/20 and Admp/Gdf1/3-r activity, respectively. Although no differential inputs of Admp, Gdf1/3-r and Fgf9/16/20 signaling were expected under this experimental condition, Otx was expressed specifically in the neural lineage. Thus, direct cell–cell interactions through Efna.d play a critical role in patterning the ectoderm of the early ascidian embryo.
机译:多个信号分子的复杂系统通常在动物胚胎中产生差异基因表达模式。在阿立迪亚胚胎中,四个信号配体,Ephrin-A.D(EFNA.D),FGF9 / 16/20,ADMP和GDF1 / 3-R,在32细胞阶段的神经谱系中协调诱导OTX表达。但是,尚未确定所有这些信令路径的差分输入是否真的需要。这些信号传导途径中的一个是足够的差异激活,并且剩余的信令途径在类似水平的所有细胞中被激活。为了解决这个问题,我们开发了一种用于确定本研究中OTX表达式的布尔函数的可参数方法。我们将信令路径的活动视为布尔值,我们还考虑了所有可能的信令梯度模式。我们成功确定了一个布尔功能,解释了32个细胞阶段的野生型和美氏胚胎动物半球中的OTX表达。这种布尔函数与三种感测模式不符合不一致,其表示单个细胞是否接收到足量的信号分子。这些感测模式表明,神经谱系中OTX的差异表达主要由EFNA.D确定,但不是通过FGF9 / 16/20,ADMP和GDF1 / 3-R信号的差分输入。为了实验证实这一假设,我们同时被击倒,GDF1 / 3-R和FGF9 / 16/20,并用重组BFGF和BMP4蛋白处理了这一三重晶体,其模仿FGF9 / 16/20并允许/ GDF1 / 3-R活动分别。尽管在该实验条件下,预计在该实验条件下预期GDF1 / 3-R和FGF9 / 16/20信号传导的差异输入,但OTX在神经谱系中特别表达。因此,通过EFNA的直接细胞 - 细胞相互作用在图案化早期的阿立迪亚胚胎的外胚层中起着关键作用。

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