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Theoretical and experimental evidence indicates that there is no detectable auxin gradient in the angiosperm female gametophyte

机译:理论和实验证据表明被子植物雌配子体中没有可检测的生长素梯度

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摘要

The plant life cycle alternates between a diploid sporophytic and a haploid gametophytic generation. The female gametophyte (FG) of flowering plants is typically formed through three syncytial mitoses, followed by cellularisation that forms seven cells belonging to four cell types. The specification of cell fates in the FG has been suggested to depend on positional information provided by an intrinsic auxin concentration gradient. The goal of this study was to develop mathematical models that explain the formation of this gradient in a syncytium. Two factors were proposed to contribute to the maintenance of the auxin gradient in Arabidopsis FGs: polar influx at early stages and localised auxin synthesis at later stages. However, no gradient could be generated using classical, one-dimensional theoretical models under these assumptions. Thus, we tested other hypotheses, including spatial confinement by the large central vacuole, background efflux and localised degradation, and investigated the robustness of cell specification under different parameters and assumptions. None of the models led to the generation of an auxin gradient that was steep enough to allow sufficiently robust patterning. This led us to re-examine the response to an auxin gradient in developing FGs using various auxin reporters, including a novel degron-based reporter system. In agreement with the predictions of our models, auxin responses were not detectable within the FG of Arabidopsis or maize, suggesting that the effects of manipulating auxin production and response on cell fate determination might be indirect.
机译:植物的生命周期在二倍体孢子体和单倍体配子体世代之间交替。开花植物的雌配子体(FG)通常是通过三个合胞体有丝分裂形成的,然后进行细胞化作用,形成七个属于四种细胞类型的细胞。已经提出FG中细胞命运的规格取决于内在生长素浓度梯度提供的位置信息。这项研究的目的是建立能够解释合胞体中这种梯度形成的数学模型。提出了两个因素来维持拟南芥FG中的生长素梯度:早期的极地涌入和后期的局部生长素合成。但是,在这些假设下,使用经典的一维理论模型无法生成梯度。因此,我们测试了其他假设,包括通过大型中央液泡进行的空间限制,背景外排和局部降解,并研究了在不同参数和假设下细胞规格的稳健性。没有一个模型导致生长素梯度的产生,该生长素梯度足够陡峭以允许足够鲁棒的图案。这导致我们使用各种生长素报告基因,包括基于德格隆的新型报告系统,重新审查了发育中的FG中对生长素梯度的反应。与我们模型的预测一致,在拟南芥或玉米的FG中未检测到生长素反应,这表明操纵生长素产生和反应对细胞命运的确定可能是间接的。

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