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黄花烟 α-氧化酶 1 通过其产生的 2-羟基亚麻酸,是植物对烟青虫幼虫攻击保持完整防御表达所必需的。

Nicotiana attenuata α-DIOXYGENASE1 through its production of 2-hydroxylinolenic acid is required for intact plant defense expression against attack from Manduca sexta larvae.

机构信息

Department of Molecular Ecology, Max Planck Institute for Chemical Ecology, Hans-Knöll-Strasse 8, D-07745, Jena, Germany.

Institute of Biology, Dahlem Centre of Plant Sciences, Freie Universität Berlin, Haderslebener Strasse 9, 12169, Berlin, Germany.

出版信息

New Phytol. 2012 Oct;196(2):574-585. doi: 10.1111/j.1469-8137.2012.04286.x. Epub 2012 Aug 31.

Abstract

Nicotiana attenuata α-DIOXYGENASE1 (α-DOX1) is an oxylipin-forming gene elicited during herbivory by fatty acid amino acid conjugates (FACs) contained in oral secretions of Manduca sexta. To understand the roles of Naα-DOX1 and its major product, 2-hydroxylinolenic acid (2-hydroxylinolenic acid), in N. attenuata's anti-herbivore defenses, we used a transgenic line specifically silenced in Naα-DOX1 expression (ir-α-dox1) and monitored 2-HOT production in M. sexta-damaged tissues and its role in influencing the production of direct defense compounds and resistance to this insect. Attack by M. sexta larvae amplified 2-HOT formation at the feeding sites; a reaction probably facilitated by Naα-DOX1's high pH optimum which allows 2-HOT formation to occur in the more alkaline conditions at the feeding sites or potentially in the insect mouth parts after the leaf tissue is ingested. Manduca sexta larvae performed better on ir-α-dox1 plants than on wild-type (WT) plants as a result of attenuated herbivory-specific JA and 2-HOT bursts as well as JA-inducible well-established defenses (nicotine, caffeoylputrescine and trypsin proteinase inhibitors). Repeated applications of 2-HOT to wounds before insect feeding partly amplified JA-controlled defenses and restored the resistance of ir-α-dox1 plants. We conclude that 2-HOT, produced by attack-activated α-DOX1 activity, participates in defense activation during insect feeding.

摘要

黄花烟 α-双加氧酶 1(α-DOX1)是一种脂氧素形成基因,在烟蚜吸食的唾液中所含的脂肪酸-氨基酸轭合物(FACs)的作用下被诱导表达。为了了解 Naα-DOX1 及其主要产物 2-羟基亚麻酸(2-HOT)在黄花烟抗虫防御中的作用,我们使用了一种特异性沉默 Naα-DOX1 表达的转基因系(ir-α-dox1),并监测了 M. sexta 损伤组织中 2-HOT 的产生及其对影响直接防御化合物的产生和对这种昆虫的抗性的作用。烟蚜幼虫的攻击增强了 2-HOT 在取食部位的形成;这一反应可能是由于 Naα-DOX1 的高 pH 最适值促进的,该最适值允许 2-HOT 在取食部位的碱性条件下形成,或者在叶片组织被摄入后,可能在昆虫的口器中形成。由于减弱的与取食相关的 JA 和 2-HOT 爆发以及 JA 诱导的成熟防御(尼古丁、咖啡酰腐胺和胰蛋白酶蛋白酶抑制剂),烟蚜幼虫在 ir-α-dox1 植株上的表现优于野生型(WT)植株。2-HOT 在昆虫取食前反复应用于伤口部分放大了 JA 控制的防御,并恢复了 ir-α-dox1 植株的抗性。我们得出结论,2-HOT 是由攻击激活的α-DOX1 活性产生的,参与了昆虫取食期间的防御激活。

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