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拟南芥保卫细胞中三聚体 G 蛋白对 ROS 信号和钙电流的调节。

Heterotrimeric G-protein regulation of ROS signalling and calcium currents in Arabidopsis guard cells.

机构信息

Biology Department, Penn State University, 208 Mueller Laboratory, University Park, PA 16802, USA.

出版信息

J Exp Bot. 2011 Apr;62(7):2371-9. doi: 10.1093/jxb/erq424. Epub 2011 Jan 24.

DOI:10.1093/jxb/erq424
PMID:21262908
Abstract

Heterotrimeric G proteins composed of Gα, Gβ, and Gγ subunits are important signalling agents in both animals and plants. In plants, G proteins modulate numerous responses, including abscisic acid (ABA) and pathogen-associated molecular pattern (PAMP) regulation of guard cell ion channels and stomatal apertures. Previous analyses of mutants deficient in the sole canonical Arabidopsis Gα subunit, GPA1, have shown that Gα-deficient guard cells are impaired in ABA inhibition of K(+) influx channels, and in pH-independent activation of anion efflux channels. ABA-induced Ca(2+) uptake through ROS-activated Ca(2+)-permeable channels in the plasma membrane is another key component of ABA signal transduction in guard cells, but the question of whether these channels are also dependent on Gα for their ABA response has not been evaluated previously. We used two independent Arabidopsis T-DNA null mutant lines, gpa1-3 and gpa1-4, to investigate this issue. We observed that gpa1 mutants are disrupted both in ABA-induced Ca(2+)-channel activation, and in production of reactive oxygen species (ROS) in response to ABA. However, in response to exogenous H(2)O(2) application, I(Ca) channels are activated normally in gpa1 guard cells. In addition, H(2)O(2) inhibition of stomatal opening and promotion of stomatal closure are not disrupted in gpa1 mutant guard cells. These data indicate that absence of GPA1 interrupts ABA signalling between ABA reception and ROS production, with a consequent impairment in Ca(2+)-channel activation.

摘要

三聚体 G 蛋白由 Gα、Gβ 和 Gγ 亚基组成,是动物和植物中重要的信号转导因子。在植物中,G 蛋白调节许多反应,包括脱落酸(ABA)和病原体相关分子模式(PAMP)对保卫细胞离子通道和气孔开度的调节。以前对唯一的拟南芥 Gα 亚基 GPA1 缺失突变体的分析表明,Gα 缺陷的保卫细胞在 ABA 抑制 K(+)内流通道和 pH 独立激活阴离子外排通道方面受损。ABA 通过质膜中 ROS 激活的 Ca(2+)渗透性通道诱导的 Ca(2+)摄取是保卫细胞 ABA 信号转导的另一个关键组成部分,但这些通道是否也依赖 Gα 来响应 ABA 以前尚未得到评估。我们使用两个独立的拟南芥 T-DNA 缺失突变体系 gpa1-3 和 gpa1-4 来研究这个问题。我们观察到,gpa1 突变体在 ABA 诱导的 Ca(2+)通道激活以及 ABA 响应中的活性氧(ROS)产生方面都受到破坏。然而,在外源 H(2)O(2)应用时,gpa1 保卫细胞中的 I(Ca)通道正常激活。此外,gpa1 突变体保卫细胞中 H(2)O(2)抑制气孔张开和促进气孔关闭的作用没有受到破坏。这些数据表明,缺乏 GPA1 中断了 ABA 信号从 ABA 受体到 ROS 产生之间的传递,导致 Ca(2+)通道激活受损。

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