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反应性羰基物种作为 H2O2 产生下游的信号介质发挥作用,并调节拟南芥保卫细胞中 ABA 信号通路中的 [Ca2+]cyt 升高。

Reactive Carbonyl Species Function as Signal Mediators Downstream of H2O2 Production and Regulate [Ca2+]cyt Elevation in ABA Signal Pathway in Arabidopsis Guard Cells.

机构信息

Graduate School of Environmental and Life Science, Okayama University, 1-1-1 Tsushima-Naka, Okayama, Japan.

Department of Agronomy, Bangabandhu Sheikh Mujibur Rahman Agricultural University, Gazipur, Bangladesh.

出版信息

Plant Cell Physiol. 2019 May 1;60(5):1146-1159. doi: 10.1093/pcp/pcz031.

DOI:10.1093/pcp/pcz031
PMID:30796836
Abstract

We have demonstrated that reactive carbonyl species (RCS) function as an intermediate downstream of hydrogen peroxide (H2O2) production in abscisic acid (ABA) signaling for stomatal closure in guard cells using transgenic tobacco plants overexpressing alkenal reductase. We investigated the conversion of the RCS production into downstream signaling events in the guard cells. Both ABA and H2O2 induced production of the RCS, such as acrolein and 4-hydroxy-(E)-2-nonenal (HNE), in epidermal tissues of wild-type Arabidopsis thaliana plants. Application of the RCS scavengers, carnosine and pyridoxamine, did not affect the ABA-induced H2O2 production but inhibited the ABA- and H2O2-induced stomatal closure. Both acrolein and HNE induced stomatal closure in a plasma membrane NAD(P)H oxidase mutant atrbohD atrbohF as well as in the wild type, but not in a calcium-dependent kinase mutant cpk6. Acrolein activated plasma membrane Ca2+-permeable cation channels, triggered cytosolic free Ca2+ concentration ([Ca2+]cyt) elevation, and induced stomatal closure accompanied by depletion of glutathione in the guard cells. These results suggest that RCS production is a signaling event between the ROS production and [Ca2+]cyt elevation during guard cell ABA signaling.

摘要

我们已经证明,在保卫细胞中,活性羰基物质(RCS)作为过氧化氢(H2O2)产生下游的中间体,在脱落酸(ABA)信号转导中发挥作用,这是使用过表达烯醛还原酶的转基因烟草植物实现的。我们研究了 RCS 产生向保卫细胞中下游信号事件的转化。ABA 和 H2O2 均诱导产生 RCS,如丙烯醛和 4-羟基-(E)-2-壬烯醛(HNE),在野生型拟南芥表皮组织中。RCS 清除剂肌肽和吡哆胺的应用并不影响 ABA 诱导的 H2O2 产生,但抑制了 ABA 和 H2O2 诱导的气孔关闭。丙烯醛和 HNE 均可诱导质膜 NAD(P)H 氧化酶突变体 atrbohD atrbohF 以及野生型中的气孔关闭,但不能诱导钙依赖性激酶突变体 cpk6 中的气孔关闭。丙烯醛激活质膜 Ca2+渗透性阳离子通道,引发细胞质游离 Ca2+浓度 ([Ca2+]cyt) 升高,并诱导气孔关闭,同时保卫细胞中谷胱甘肽耗竭。这些结果表明,RCS 产生是保卫细胞 ABA 信号转导过程中 ROS 产生和 [Ca2+]cyt 升高之间的信号事件。

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