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Shapeshifting in the Venus flytrap (): Morphological and biomechanical adaptations and the potential costs of a failed hunting cycle.捕蝇草的形态变化:形态学与生物力学适应性以及捕猎周期失败的潜在代价
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The effect of abscisic acid on cell turgor pressures, solute content and growth of wheat roots.脱落酸对小麦根细胞膨压、溶质含量和生长的影响。
Planta. 1987 Feb;170(2):257-62. doi: 10.1007/BF00397896.
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The action potential of Dionaea muscipula Ellis.捕蝇草的动作电位。
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Trap-closing chemical factors of the Venus flytrap (Dionaea muscipulla Ellis).捕蝇草(茅膏菜科捕蝇草属埃利斯)的陷阱关闭化学因子
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AtALMT12 represents an R-type anion channel required for stomatal movement in Arabidopsis guard cells.AtALMT12 代表了拟南芥保卫细胞中气孔运动所必需的 R 型阴离子通道。
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The Pseudomonas syringae phytotoxin coronatine promotes virulence by overcoming salicylic acid-dependent defences in Arabidopsis thaliana.丁香假单胞菌植物毒素冠菌素通过克服拟南芥中水杨酸依赖的防御来促进毒力。
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Guard cell anion channel SLAC1 is regulated by CDPK protein kinases with distinct Ca2+ affinities.保卫细胞阴离子通道 SLAC1 受具有不同 Ca2+ 亲和力的 CDPK 蛋白激酶调节。
Proc Natl Acad Sci U S A. 2010 Apr 27;107(17):8023-8. doi: 10.1073/pnas.0912030107. Epub 2010 Apr 12.
8
Activity of guard cell anion channel SLAC1 is controlled by drought-stress signaling kinase-phosphatase pair.保卫细胞阴离子通道 SLAC1 的活性受干旱胁迫信号激酶-磷酸酶对的控制。
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Nature. 2009 Dec 3;462(7273):660-4. doi: 10.1038/nature08599. Epub 2009 Nov 18.
10
Velocity estimates for signal propagation leading to systemic jasmonic acid accumulation in wounded Arabidopsis.导致受伤拟南芥中系统性茉莉酸积累的信号传播速度估计。
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一对特殊的植物激素控制捕蝇草的兴奋性、缓慢关闭和外部胃的形成。

A special pair of phytohormones controls excitability, slow closure, and external stomach formation in the Venus flytrap.

机构信息

Institute for Molecular Plant Physiology and Biophysics, University Wuerzburg, D-97070 Wuerzburg, Germany.

出版信息

Proc Natl Acad Sci U S A. 2011 Sep 13;108(37):15492-7. doi: 10.1073/pnas.1112535108. Epub 2011 Sep 6.

DOI:10.1073/pnas.1112535108
PMID:21896747
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3174645/
Abstract

Venus flytrap's leaves can catch an insect in a fraction of a second. Since the time of Charles Darwin, scientists have struggled to understand the sensory biology and biomechanics of this plant, Dionaea muscipula. Here we show that insect-capture of Dionaea traps is modulated by the phytohormone abscisic acid (ABA) and jasmonates. Water-stressed Dionaea, as well as those exposed to the drought-stress hormone ABA, are less sensitive to mechanical stimulation. In contrast, application of 12-oxo-phytodienoic acid (OPDA), a precursor of the phytohormone jasmonic acid (JA), the methyl ester of JA (Me-JA), and coronatine (COR), the molecular mimic of the isoleucine conjugate of JA (JA-Ile), triggers secretion of digestive enzymes without any preceding mechanical stimulus. Such secretion is accompanied by slow trap closure. Under physiological conditions, insect-capture is associated with Ca(2+) signaling and a rise in OPDA, Apparently, jasmonates bypass hapto-electric processes associated with trap closure. However, ABA does not affect OPDA-dependent gland activity. Therefore, signals for trap movement and secretion seem to involve separate pathways. Jasmonates are systemically active because application to a single trap induces secretion and slow closure not only in the given trap but also in all others. Furthermore, formerly touch-insensitive trap sectors are converted into mechanosensitive ones. These findings demonstrate that prey-catching Dionaea combines plant-specific signaling pathways, involving OPDA and ABA with a rapidly acting trigger, which uses ion channels, action potentials, and Ca(2+) signals.

摘要

捕蝇草的叶子可以在瞬间捕捉到昆虫。自查尔斯·达尔文时代以来,科学家们一直在努力研究这种植物——腺毛捕蝇草的感觉生物学和生物力学。在这里,我们表明,昆虫捕捉捕蝇草陷阱受到植物激素脱落酸 (ABA) 和茉莉酸的调节。处于缺水胁迫状态的捕蝇草,以及那些暴露在干旱胁迫激素 ABA 下的捕蝇草,对机械刺激的敏感性降低。相比之下,应用 12-氧-植物二烯酸(OPDA),一种植物激素茉莉酸(JA)的前体,JA 的甲酯(Me-JA)和冠菌素(COR),JA 的异亮氨酸轭合物(JA-Ile)的分子模拟物,会在没有任何先前机械刺激的情况下触发消化酶的分泌。这种分泌伴随着缓慢的陷阱关闭。在生理条件下,昆虫的捕获与 Ca(2+)信号和 OPDA 的增加有关,显然,茉莉酸盐绕过了与陷阱关闭相关的触觉-电过程。然而,ABA 并不影响依赖 OPDA 的腺体活动。因此,陷阱运动和分泌的信号似乎涉及不同的途径。茉莉酸盐是全身性的,因为应用于单个陷阱不仅会引起该特定陷阱的分泌和缓慢关闭,而且还会引起所有其他陷阱的分泌和缓慢关闭。此外,以前对触摸不敏感的陷阱扇区变成了机械敏感的扇区。这些发现表明,捕食性的捕蝇草结合了植物特有的信号通路,涉及 OPDA 和 ABA 以及一个快速作用的触发机制,该机制使用离子通道、动作电位和 Ca(2+)信号。