An auxin homeostat allows plant cells to establish and control defined transmembrane auxin gradients

IF 8.3 1区 生物学 Q1 PLANT SCIENCES
New Phytologist Pub Date : 2024-09-15 DOI:10.1111/nph.20120
Markus Geisler, Ingo Dreyer
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引用次数: 0

Abstract

  • Extracellular auxin maxima and minima are important to control plant developmental programs. Auxin gradients are provided by the concerted action of proteins from the three major plasma membrane (PM) auxin transporter classes AUX1/LAX, PIN and ATP-BINDING CASSETTE subfamily B (ABCB) transporters. But neither genetic nor biochemical nor modeling approaches have been able to reliably assign the individual roles and interplay of these transporter types.
  • Based on the thermodynamic properties of the transporters, we show here by mathematical modeling and computational simulations that the concerted action of different auxin transporter types allows the adjustment of specific transmembrane auxin gradients. The dynamic flexibility of the ‘auxin homeostat’ comes at the cost of an energy-consuming ‘auxin cycling’ across the membrane.
  • An unexpected finding was that potential functional ABCB-PIN synchronization appears to allow an optimization of the trade-off between the speed of PM auxin gradient adjustment on the one hand and ATP consumption and disturbance of general anion homeostasis on the other.
  • In conclusion, our analyses provide fundamental insights into the thermodynamic constraints and flexibility of transmembrane auxin transport in plants.
植物细胞可以利用植物生长调节剂建立并控制确定的跨膜植物生长调节剂梯度。
细胞外辅助素的最大值和最小值对控制植物发育程序非常重要。AUX1/LAX、PIN 和 ATP-BINDING CASSETTE 亚家族 B(ABCB)转运体这三大类质膜(PM)辅助素转运蛋白的协同作用提供了辅助素梯度。但是,无论是遗传学方法、生物化学方法还是建模方法,都无法可靠地确定这些转运体类型的各自作用和相互影响。基于转运体的热力学特性,我们在此通过数学建模和计算模拟表明,不同类型的辅助素转运体协同作用可调节特定的跨膜辅助素梯度。而 "辅素同态 "的动态灵活性是以消耗能量的跨膜 "辅素循环 "为代价的。一个意想不到的发现是,潜在的功能性 ABCB-PIN 同步似乎允许在 PM auxin 梯度调节速度与 ATP 消耗和一般阴离子平衡紊乱之间进行优化权衡。总之,我们的分析为了解植物跨膜辅助素转运的热力学限制和灵活性提供了基本见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
New Phytologist
New Phytologist 生物-植物科学
自引率
5.30%
发文量
728
期刊介绍: New Phytologist is an international electronic journal published 24 times a year. It is owned by the New Phytologist Foundation, a non-profit-making charitable organization dedicated to promoting plant science. The journal publishes excellent, novel, rigorous, and timely research and scholarship in plant science and its applications. The articles cover topics in five sections: Physiology & Development, Environment, Interaction, Evolution, and Transformative Plant Biotechnology. These sections encompass intracellular processes, global environmental change, and encourage cross-disciplinary approaches. The journal recognizes the use of techniques from molecular and cell biology, functional genomics, modeling, and system-based approaches in plant science. Abstracting and Indexing Information for New Phytologist includes Academic Search, AgBiotech News & Information, Agroforestry Abstracts, Biochemistry & Biophysics Citation Index, Botanical Pesticides, CAB Abstracts®, Environment Index, Global Health, and Plant Breeding Abstracts, and others.
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