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首页> 外文期刊>eLife journal >Calcium specificity signaling mechanisms in abscisic acid signal transduction in Arabidopsis guard cells
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Calcium specificity signaling mechanisms in abscisic acid signal transduction in Arabidopsis guard cells

机译:拟南芥保卫细胞脱落酸信号转导中的钙特异性信号转导机制

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Plant leaves have tiny openings or pores called stomata, which allow carbon dioxide, water vapor and other gases to diffuse in and out of the plant. Two cells called guard cells surround each stoma and control the opening and closing of the pore. If a plant is losing excessive amounts of water, for example during a drought, the plant produces a hormone called abscisic acid that promotes the closure of its stomata. When abscisic acid is present, the guard cells are sensitive to changes in their internal concentration of calcium ions so that calcium ions can activate a protein called SLAC1. This leads to responses in the guard cells that close the stoma. The calcium ions activate SLAC1 by stimulating enzymes called calcium-dependent protein kinases (CPKs). However, abscisic acid can also trigger other enzymes that can activate SLAC1 independently of the calcium ions. Calcium ions are also reported to be involved in the opening of stomata, when abscisic acid is not present. Therefore, it is not clear how abscisic acid works to specifically ‘prime’ guard cells to close the stomata in response to increases in calcium ions during drought. Brandt, Munemasa et al. studied stomata in a plant called Arabidopsis thaliana. The experiments show that, in the presence of abscisic acid, mutant plants that lack four different CPK enzymes are impaired in the activation of SLAC1 and the closing of stomata in response to increases in calcium ions. Further experiments found that other enzymes called the PP2Cs—which are switched off by abscisic acid—are responsible for regulating the Ca2+ sensitivity of guard cells. Switching off PP2Cs enables closing of the stomata in response to calcium ions. It has been suggested previously that the CPKs and the calcium-independent enzymes are involved in two separate pathways that promote the closure of stomata. However, Brandt, Munemasa et al. found that the calcium-independent enzymes are required for calcium ions to activate SLAC1 in guard cells, revealing that these two pathways are linked. Brandt, Munemasa et al.'s findings reveal how abscisic acid is able to specifically prime guard cells to close stomata in response to calcium ions. The next challenge is to understand how the CPKs and calcium-independent enzymes work together during the closure of stomata.
机译:植物的叶子上有微小的开口或气孔,称为气孔,可使二氧化碳,水蒸气和其他气体扩散进出植物。两个称为保卫细胞的细胞围绕着每个造口,并控制毛孔的打开和关闭。如果植物流失过多的水,例如在干旱期间,该植物会产生一种称为脱落酸的激素,该激素会促进其气孔的闭合。当存在脱落酸时,保卫细胞对其内部钙离子浓度的变化敏感,因此钙离子可以激活称为SLAC1的蛋白质。这导致封闭造口的保卫细胞作出反应。钙离子通过刺激称为钙依赖性蛋白激酶(CPK)的酶来激活SLAC1。但是,脱落酸还可以触发其他酶,这些酶可以独立于钙离子激活SLAC1。据报道,当不存在脱落酸时,钙离子也参与了气孔的开放。因此,尚不清楚脱落酸如何在干旱期间响应钙离子的增加而专门“启动”保卫细胞以关闭气孔。 Brandt,Munemasa等。在一种叫做拟南芥的植物中研究了气孔。实验表明,在脱落酸的存在下,缺少4种不同CPK酶的突变植物在SLAC1的激活和气孔关闭中的钙离子响应受到损害。进一步的实验发现,其他被称为PP2C的酶(被脱落酸切断)负责调节保卫细胞对Ca2 +的敏感性。关闭PP2C可以响应钙离子而关闭气孔。以前已经有人提出,CPK和不依赖钙的酶参与促进气孔关闭的两个独立途径。但是,Brandt,Munemasa等。发现钙独立的酶是钙离子激活保卫细胞中SLAC1所必需的,这表明这两个途径是相关的。 Brandt,Munemasa等人的发现揭示了脱落酸如何能够特异地引发保卫细胞响应钙离子而关闭气孔。下一个挑战是了解气孔关闭过程中CPK和不依赖钙的酶如何协同工作。

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