Phillips Michael A, Walter Michael H, Ralph Steven G, Dabrowska Paulina, Luck Katrin, Urós Eva Maria, Boland Wilhelm, Strack Dieter, Rodríguez-Concepción Manuel, Bohlmann Jörg, Gershenzon Jonathan
Max Planck Institut für Chemische Okologie, Abteilung Biochemie, Hans Knöll Str. 8, Jena, 07745, Germany.
Plant Mol Biol. 2007 Oct;65(3):243-57. doi: 10.1007/s11103-007-9212-5. Epub 2007 Aug 9.
Conifers produce terpenoid-based oleoresins as constitutive and inducible defenses against herbivores and pathogens. Much information is available about the genes and enzymes of the late steps of oleoresin terpenoid biosynthesis in conifers, but almost nothing is known about the early steps which proceed via the methylerythritol phosphate (MEP) pathway. Here we report the cDNA cloning and functional identification of three Norway spruce (Picea abies) genes encoding 1-deoxy-D-xylulose 5-phosphate synthase (DXS), which catalyzes the first step of the MEP pathway, and their differential expression in the stems of young saplings. Among them are representatives of both types of plant DXS genes. A single type I DXS gene is constitutively expressed in bark tissue and not affected by wounding or fungal application. In contrast, two distinct type II DXS genes, PaDXS2A and PaDXS2B, showed increased transcript abundance after these treatments as did two other genes of the MEP pathway tested, 1-deoxy-D-xylulose 5-phosphate reductoisomerase (DXR) and 4-hydroxyl 3-methylbutenyl diphosphate reductase (HDR). We also measured gene expression in a Norway spruce cell suspension culture system that, like intact trees, accumulates monoterpenes after treatment with methyl jasmonate. These cell cultures were characterized by an up-regulation of monoterpene synthase gene transcripts and enzyme activity after elicitor treatment, as well as induced formation of octadecanoids, including jasmonic acid and 12-oxophytodienoic acid. Among the Type II DXS genes in cell cultures, PaDXS2A was induced by treatment with chitosan, methyl salicylate, and Ceratocystis polonica (a bark beetle-associated, blue-staining fungal pathogen of Norway spruce). However, PaDXS2B was induced by treatment with methyl jasmonate and chitosan, but was not affected by methyl salicylate or C. polonica. Our results suggest distinct functions of the three DXS genes in primary and defensive terpenoid metabolism in Norway spruce.
针叶树产生基于萜类化合物的油性树脂,作为对食草动物和病原体的组成性和诱导性防御。关于针叶树油性树脂萜类生物合成后期步骤的基因和酶,已有很多信息,但对于通过甲基赤藓糖醇磷酸(MEP)途径进行的早期步骤却几乎一无所知。在此,我们报告了三个挪威云杉(Picea abies)基因的cDNA克隆及功能鉴定,这三个基因编码1-脱氧-D-木酮糖-5-磷酸合酶(DXS),该酶催化MEP途径的第一步,以及它们在幼树茎中的差异表达。其中包括两种类型植物DXS基因的代表。单个I型DXS基因在树皮组织中组成性表达,不受创伤或真菌接种的影响。相比之下,两个不同的II型DXS基因,PaDXS2A和PaDXS2B,在这些处理后转录本丰度增加,另外两个测试的MEP途径基因,1-脱氧-D-木酮糖-5-磷酸还原异构酶(DXR)和4-羟基-3-甲基丁烯基二磷酸还原酶(HDR)也是如此。我们还在挪威云杉细胞悬浮培养系统中测量了基因表达,该系统与完整树木一样,在用茉莉酸甲酯处理后积累单萜。这些细胞培养物的特征是在诱导剂处理后单萜合酶基因转录本和酶活性上调,以及诱导形成十八碳类化合物,包括茉莉酸和12-氧代植物二烯酸。在细胞培养物中的II型DXS基因中,PaDXS2A通过壳聚糖、水杨酸甲酯和云杉短喙木蠹蛾(一种与挪威云杉树皮甲虫相关的蓝变真菌病原体)处理诱导。然而,PaDXS2B通过茉莉酸甲酯和壳聚糖处理诱导,但不受水杨酸甲酯或云杉短喙木蠹蛾的影响。我们的结果表明,这三个DXS基因在挪威云杉的初级和防御性萜类代谢中具有不同的功能。