Stoma Szymon, Lucas Mikael, Chopard Jérôme, Schaedel Marianne, Traas Jan, Godin Christophe
Virtual Plants Project-Team, UMR DAP, INRIA, Montpellier, France.
PLoS Comput Biol. 2008 Oct;4(10):e1000207. doi: 10.1371/journal.pcbi.1000207. Epub 2008 Oct 31.
Plants continuously generate new organs through the activity of populations of stem cells called meristems. The shoot apical meristem initiates leaves, flowers, and lateral meristems in highly ordered, spiralled, or whorled patterns via a process called phyllotaxis. It is commonly accepted that the active transport of the plant hormone auxin plays a major role in this process. Current hypotheses propose that cellular hormone transporters of the PIN family would create local auxin maxima at precise positions, which in turn would lead to organ initiation. To explain how auxin transporters could create hormone fluxes to distinct regions within the plant, different concepts have been proposed. A major hypothesis, canalization, proposes that the auxin transporters act by amplifying and stabilizing existing fluxes, which could be initiated, for example, by local diffusion. This convincingly explains the organised auxin fluxes during vein formation, but for the shoot apical meristem a second hypothesis was proposed, where the hormone would be systematically transported towards the areas with the highest concentrations. This implies the coexistence of two radically different mechanisms for PIN allocation in the membrane, one based on flux sensing and the other on local concentration sensing. Because these patterning processes require the interaction of hundreds of cells, it is impossible to estimate on a purely intuitive basis if a particular scenario is plausible or not. Therefore, computational modelling provides a powerful means to test this type of complex hypothesis. Here, using a dedicated computer simulation tool, we show that a flux-based polarization hypothesis is able to explain auxin transport at the shoot meristem as well, thus providing a unifying concept for the control of auxin distribution in the plant. Further experiments are now required to distinguish between flux-based polarization and other hypotheses.
植物通过被称为分生组织的干细胞群体的活动不断产生新器官。茎尖分生组织通过一种称为叶序的过程,以高度有序、螺旋状或轮状模式启动叶片、花朵和侧生分生组织。人们普遍认为植物激素生长素的主动运输在这一过程中起主要作用。目前的假说提出,PIN家族的细胞激素转运蛋白会在精确位置产生局部生长素最大值,进而导致器官起始。为了解释生长素转运蛋白如何在植物内将激素通量导向不同区域,人们提出了不同的概念。一个主要假说,即输导组织形成学说,提出生长素转运蛋白通过放大和稳定现有通量来发挥作用,例如,这些通量可以由局部扩散启动。这令人信服地解释了叶脉形成过程中有组织的生长素通量,但对于茎尖分生组织,人们提出了另一个假说,即激素会系统地运输到浓度最高的区域。这意味着在膜中PIN分配存在两种截然不同的机制,一种基于通量感知而另一种基于局部浓度感知。由于这些模式形成过程需要数百个细胞的相互作用,仅凭直观判断特定情况是否合理是不可能的。因此,计算建模为检验这类复杂假说提供了有力手段。在这里,我们使用专门的计算机模拟工具表明,基于通量的极化假说也能够解释茎尖分生组织处的生长素运输,从而为植物中生长素分布的控制提供了一个统一的概念。现在需要进一步的实验来区分基于通量的极化假说和其他假说。