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丙二烯氧化物合酶的敲除突变导致拟南芥雄性不育和伤口信号转导缺陷,这是由于茉莉酸生物合成受阻所致。

A knock-out mutation in allene oxide synthase results in male sterility and defective wound signal transduction in Arabidopsis due to a block in jasmonic acid biosynthesis.

作者信息

Park Joon-Hyun, Halitschke Rayko, Kim Ho Bang, Baldwin Ian T, Feldmann Kenneth A, Feyereisen René

机构信息

Ceres Inc., 3007 Malibu Canyon Road, Malibu, CA 90265, USA.

出版信息

Plant J. 2002 Jul;31(1):1-12. doi: 10.1046/j.1365-313x.2002.01328.x.

Abstract

Recent studies on jasmonic acid (JA) biosynthetic mutants have shown that jasmonates play essential roles in pollen maturation and dehiscence and wound-induced defence against biotic attacks. To better understand the biosynthetic mechanisms of this essential plant hormone, we isolated an Arabidopsis knock-out mutant defective in the JA biosynthetic gene CYP74A (allene oxide synthase, AOS) using reverse genetics screening methods. This enzyme catalyses dehydration of the hydroperoxide to an unstable allene oxide in the JA biosynthetic pathway. Endogenous JA levels, which increase 100-fold 1 h after wounding in wild-type plants, do not increase after wounding in the aos mutant. In addition, the mutant showed severe male sterility due to defects in anther and pollen development. The male-sterile phenotype was completely rescued by exogenous application of methyl jasomonate and by complementation with constitutive expression of the AOS gene. RT-PCR analysis showed that the induction of transcripts for vegetative storage protein and lipoxygenase genes, previously shown to be inducible by wound and jasmonate application in the wild-type, was absent in the aos mutant. In transgenic plants constitutively expressing AOS, wound-induced JA levels were 50-100% higher compared to wild-type plants. Taken together with JA deficiency in the aos mutant, our results show that AOS is critical for the biosynthesis of all biologically active jasmonates. Our results also suggest that AOS expression is limiting JA levels in wounded plants, but that the AOS hydroperoxide substrate levels, controlled by upstream enzymes (lipoxygenase and phospholipase), determine JA levels in unwounded plants.

摘要

近期关于茉莉酸(JA)生物合成突变体的研究表明,茉莉酸类物质在花粉成熟、开裂以及伤口诱导的抵御生物攻击的防御反应中发挥着重要作用。为了更好地理解这种重要植物激素的生物合成机制,我们利用反向遗传学筛选方法,分离出了拟南芥中一个在JA生物合成基因CYP74A(丙二烯氧化物合酶,AOS)上存在缺陷的敲除突变体。该酶在JA生物合成途径中催化氢过氧化物脱水生成不稳定的丙二烯氧化物。野生型植物在受伤1小时后内源性JA水平会增加100倍,而aos突变体在受伤后JA水平并未增加。此外,该突变体由于花药和花粉发育缺陷而表现出严重的雄性不育。通过外源施加茉莉酸甲酯以及用AOS基因的组成型表达进行互补,可完全挽救雄性不育表型。RT-PCR分析表明,在野生型中先前已证明可被伤口和茉莉酸诱导的营养贮藏蛋白和脂氧合酶基因的转录本诱导,在aos突变体中并不存在。在组成型表达AOS的转基因植物中,伤口诱导的JA水平比野生型植物高50 - 100%。综合aos突变体中JA缺乏的情况,我们的结果表明AOS对于所有具有生物活性的茉莉酸类物质的生物合成至关重要。我们的结果还表明,AOS的表达限制了受伤植物中的JA水平,但由上游酶(脂氧合酶和磷脂酶)控制的AOS氢过氧化物底物水平决定了未受伤植物中的JA水平。

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