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Cooperative Function of PLDδ and PLDα1 in Abscisic Acid-Induced Stomatal Closure in Arabidopsis1[W][OA]

机译:PLDδ和PLDα1在拟南芥中由脱落酸诱导的气孔关闭中的协同作用[W] [OA]

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摘要

Phospholipase D (PLD) is involved in responses to abiotic stress and abscisic acid (ABA) signaling. To investigate the roles of two Arabidopsis (Arabidopsis thaliana) PLDs, PLDα1 and PLDδ, in ABA signaling in guard cells, we analyzed ABA responses in guard cells using Arabidopsis wild type, pldα1 and pldδ single mutants, and a pldα1 pldδ double mutant. ABA-induced stomatal closure was suppressed in the pldα1 pldδ double mutant but not in the pld single mutants. The pldα1 and pldδ mutations reduced ABA-induced phosphatidic acid production in epidermal tissues. Expression of either PLDα1 or PLDδ complemented the double mutant stomatal phenotype. ABA-induced stomatal closure in both pldα1 and pldδ single mutants was inhibited by a PLD inhibitor (1-butanol ), suggesting that both PLDα1 and PLDδ function in ABA-induced stomatal closure. During ABA-induced stomatal closure, wild-type guard cells accumulate reactive oxygen species and nitric oxide and undergo cytosolic alkalization, but these changes are reduced in guard cells of the pldα1 pldδ double mutant. Inward-rectifying K+ channel currents of guard cells were inhibited by ABA in the wild type but not in the pldα1 pldδ double mutant. ABA inhibited stomatal opening in the wild type and the pldδ mutant but not in the pldα1 mutant. In wild-type rosette leaves, ABA significantly increased PLDδ transcript levels but did not change PLDα1 transcript levels. Furthermore, the pldα1 and pldδ mutations mitigated ABA inhibition of seed germination. These results suggest that PLDα1 and PLDδ cooperate in ABA signaling in guard cells but that their functions do not completely overlap.
机译:磷脂酶D(PLD)参与对非生物胁迫和脱落酸(ABA)信号的响应。为了研究两个拟南芥(Arabidopsis thaliana)PLD,PLDα1和PLDδ在保卫细胞ABA信号中的作用,我们使用拟南芥属野生型pldα1和pldδ单突变体以及pldα1pldδ双突变体分析了保卫细胞中的ABA反应。 ABA诱导的气孔关闭在pldα1pldδ双突变体中被抑制,而在pld单突变体中则没有。 pldα1和pldδ突变减少了表皮组织中ABA诱导的磷脂酸生成。 PLDα1或PLDδ的表达与双重突变气孔表型互补。在Pldα1和pldδ单个突变体中,ABA诱导的气孔关闭均受到PLD抑制剂(1-丁醇)的抑制,表明PLDα1和PLDδ在ABA诱导的气孔关闭中均起作用。在ABA诱导的气孔关闭过程中,野生型保卫细胞积聚活性氧和一氧化氮,并发生胞质碱化,但这些变化在pldα1pldδ双突变体的保卫细胞中减少。在野生型中,ABA抑制保卫细胞的向内整流K +通道电流,而在pldα1pldδ双突变体中则没有。 ABA抑制野生型和pldδ突变体中的气孔开放,但不抑制pldα1突变体中的气孔开放。在野生型莲座丛叶中,ABA显着增加了PLDδ转录水平,但没有改变PLDα1转录水平。此外,pldα1和pldδ突变减轻了ABA对种子发芽的抑制作用。这些结果表明PLDα1和PLDδ在保卫细胞的ABA信号转导中合作,但它们的功能并不完全重叠。

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