首页> 外文期刊>Plant Science: An International Journal of Experimental Plant Biology >Cloning of novel rice allene oxide cyclase (OsAOC): mRNA expression and comparative analysis with allene oxide synthase (OsAOS) gene provides insight into the transcriptional regulation of octadecanoid pathway biosynthetic genes in rice
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Cloning of novel rice allene oxide cyclase (OsAOC): mRNA expression and comparative analysis with allene oxide synthase (OsAOS) gene provides insight into the transcriptional regulation of octadecanoid pathway biosynthetic genes in rice

机译:水稻新型水稻烯丙氧化物环化酶(OsAOC)的克隆:mRNA表达和烯丙氧化物合酶(OsAOS)基因的比较分析可深入了解水稻中十八烷类途径生物合成基因的转录调控

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Here we cloned a novel rice (japonica-type cv. Nipponbare) cDNA highly homologous to allene oxide cyclase (AOC, EC 5.3.99.6; jasmonate biosynthetic pathway), named OsAOC. OsAOC showed significant similarity at amino acid level with the available AOCs only from the dicotyledonous tomato and Arabidopsis. Examination of the steady-state mRNA level in an early time course experiment revealed that OsA OC expressed very weakly in healthy leaves, and showed responsiveness to wounding by cut within 30 min, followed by an increase with time till 120 min. Interestingly, jasmonic acid (JA) treatment itself potently enhanced its expression over the control (wounded leaves), suggesting feedback activation of OsA OC. Other signalling components, salicylic acid (SA), ethylene (using ethephon, ET), abscisic acid (ABA), and hydrogen peroxide (H2O2), also strongly and transiently up-regulated the OsAOC transcript. Moreover, heavy metals and protein phosphatase (PP) inhibitors were potent in inducing the OsAOC transcript. A protein synthesis inhibitor, cycloheximide (CHX), alone or in combination with JA and SA further enhanced its expression. suggesting the involvement of a de novo synthesized negative regulator in its regulation. A long-term time course experiment revealed that wounding by cut was the most effective in inducing the expression of OsAOC starting at 3 h after treatment, whereas all the above pharmacological agents showed induction at 3-12 h, after which the OsA OC expression declined under light. whereas this expression was substantially suppressed under darkness. Additionally, chitosan (CT), a fungal elicitor also transiently up-regulated the OsA OC expression. Intriguingly, OsA OC mRNA expression manifested a clear rhythmicity under light/ dark cycle. Finally, parallel investigations of allene oxide synthase (OsA OS, accession number AY062258) and its comparison with OsAOC indicated their differential response to various environmental cues. These results strongly suggest a role for OsAOC (and OsAOS) in rice plant defense/stress response pathway(s). (C) 2003 Elsevier Science Ireland Ltd. All rights reserved. [References: 43]
机译:在这里,我们克隆了一个与水稻氧化烯环化酶(AOC,EC 5.3.99.6;茉莉酸酯生物合成途径)高度同源的新型水稻(粳稻型日本晴)cDNA,称为OsAOC。 OsAOC在氨基酸水平上显示出与仅来自双子叶番茄和拟南芥的可用AOC显着相似。在早期时间过程实验中对稳态mRNA水平的检查表明,OsA OC在健康叶片中表达非常弱,并且在30分钟内显示出对伤口的反应,随后随时间增加直至120分钟。有趣的是,茉莉酸(JA)处理本身比对照(受伤的叶子)有力地增强了其表达,表明OsA OC的反馈激活。其他信号成分,水杨酸(SA),乙烯(使用乙烯利,ET),脱落酸(ABA)和过氧化氢(H2O2),也强烈且瞬时上调了OsAOC转录本。此外,重金属和蛋白磷酸酶(PP)抑制剂在诱导OsAOC转录本方面很有效。单独或与JA和SA组合使用的蛋白质合成抑制剂环己酰亚胺(CHX)进一步增强了其表达。提示从头合成负调节剂参与其调节。长期的时程实验表明,在治疗后3 h,切伤最有效地诱导OsAOC的表达,而上述所有药理剂在3-12 h均表现出诱导作用,此后OsA OC的表达下降在光下。而这种表情在黑暗中被压制了。此外,壳聚糖(CT),一种真菌引发剂也瞬时上调OsA OC表达。有趣的是,OsA OC mRNA表达在明/暗周期下表现出明显的节律性。最后,对氧化烯合酶(OsA OS,登录号AY062258)进行的并行研究及其与OsAOC的比较表明,它们对各种环境线索的响应不同。这些结果强烈暗示了OsAOC(和OsAOS)在水稻植物防御/胁迫响应途径中的作用。 (C)2003 Elsevier Science Ireland Ltd.保留所有权利。 [参考:43]

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