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Phospholipase D alpha 1 and Phosphatidic Acid Regulate NADPH Oxidase Activity and Production of Reactive Oxygen Species in ABA-Mediated Stomatal Closure in Arabidopsis

机译:拟南芥ABA介导的气孔关闭中磷脂酶D alpha 1和磷脂酸调节NADPH氧化酶活性和活性氧的产生。

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摘要

We determined the role of Phospholipase D alpha 1 (PLD alpha 1) and its lipid product phosphatidic acid (PA) in abscisic acid (ABA)-induced production of reactive oxygen species (ROS) in Arabidopsis thaliana guard cells. The pld alpha 1 mutant failed to produce ROS in guard cells in response to ABA. ABA stimulated NADPH oxidase activity in wild-type guard cells but not in pld alpha 1 cells, whereas PA stimulated NADPH oxidase activity in both genotypes. PA bound to recombinant Arabidopsis NADPH oxidase RbohD (respiratory burst oxidase homolog D) and RbohF. The PA binding motifs were identified, and mutation of the Arg residues 149, 150, 156, and 157 in RbohD resulted in the loss of PA binding and the loss of PA activation of RbohD. The rbohD mutant expressing non-PA-binding RbohD was compromised in ABA-mediated ROS production and stomatal closure. Furthermore, ABA-induced production of nitric oxide (NO) was impaired in pld alpha 1 guard cells. Disruption of PA binding to ABI1 protein phosphatase 2C did not affect ABA-induced production of ROS or NO, but the PA-ABI1 interaction was required for stomatal closure induced by ABA, H2O2, or NO. Thus, PA is as a central lipid signaling molecule that links different components in the ABA signaling network in guard cells.
机译:我们确定了磷脂酶D alpha 1(PLD alpha 1)及其脂质产物磷脂酸(PA)在脱落酸(ABA)诱导的拟南芥保卫细胞中产生的活性氧(ROS)产生中的作用。 pld alpha 1突变体无法响应ABA而在保卫细胞中产生ROS。 ABA刺激野生型保卫细胞中的NADPH氧化酶活性,但不刺激pld alpha 1细胞,而PA刺激两种基因型中的NADPH氧化酶活性。 PA与重组拟南芥NADPH氧化酶RbohD(呼吸爆发氧化酶同系物D)和RbohF结合。鉴定出PA结合基序,并且RbohD中Arg残基149、150、156和157的突变导致PA结合的丧失和RbohD的PA活化的丧失。表达非PA结合RbohD的rbohD突变体在ABA介导的ROS产生和气孔关闭中受损。此外,在pld alpha 1保卫细胞中ABA诱导的一氧化氮(NO)产生受到损害。破坏PA与ABI1蛋白磷酸酶2C的结合不会影响ABA诱导的ROS或NO的产生,但PA-ABI1相互作用是ABA,H2O2或NO诱导的气孔关闭所必需的。因此,PA是连接保护细胞中ABA信号网络中不同成分的中心脂质信号分子。

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