Université de Strasbourg, CNRS, IBMP UPR 2357, F-67000, Strasbourg, France.
Institute of Biosciences and Biotechnologies, CEA-CNRS-Aix Marseille Université, UMR 7265, LB3M, F-13108, Cadarache, France.
New Phytol. 2017 Jul;215(1):173-186. doi: 10.1111/nph.14590. Epub 2017 May 12.
Epoxide hydrolases (EHs) are present in all living organisms. They have been extensively characterized in mammals; however, their biological functions in plants have not been demonstrated. Based on in silico analysis, we identified AtEH1 (At3g05600), a putative Arabidopsis thaliana epoxide hydrolase possibly involved in cutin monomer synthesis. We expressed AtEH1 in yeast and studied its localization in vivo. We also analyzed the composition of cutin from A. thaliana lines in which this gene was knocked out. Incubation of recombinant AtEH1 with epoxy fatty acids confirmed its capacity to hydrolyze epoxides of C18 fatty acids into vicinal diols. Transfection of Nicotiana benthamiana leaves with constructs expressing AtEH1 fused to enhanced green fluorescent protein (EGFP) indicated that AtEH1 is localized in the cytosol. Analysis of cutin monomers in loss-of-function Ateh1-1 and Ateh1-2 mutants showed an accumulation of 18-hydroxy-9,10-epoxyoctadecenoic acid and a concomitant decrease in corresponding vicinal diols in leaf and seed cutin. Compared with wild-type seeds, Ateh1 seeds showed delayed germination under osmotic stress conditions and increased seed coat permeability to tetrazolium red. This work reports a physiological role for a plant EH and identifies AtEH1 as a new member of the complex machinery involved in cutin synthesis.
环氧化物水解酶(EHs)存在于所有生物中。它们在哺乳动物中得到了广泛的研究;然而,它们在植物中的生物学功能尚未得到证实。通过计算机分析,我们鉴定了拟南芥 AtEH1(At3g05600),一种可能参与角质单体合成的拟南芥环氧化物水解酶。我们在酵母中表达了 AtEH1,并研究了其在体内的定位。我们还分析了该基因敲除的拟南芥系的角质组成。用环氧脂肪酸孵育重组 AtEH1 证实了其水解 C18 脂肪酸中环氧化物为邻二醇的能力。将表达 AtEH1 与增强型绿色荧光蛋白(EGFP)融合的构建体转染到黄花烟叶片中,表明 AtEH1 定位于细胞质中。在功能丧失型 Ateh1-1 和 Ateh1-2 突变体中角质单体的分析表明,18-羟基-9,10-环氧十八烯酸积累,相应的邻二醇在叶和种子角质中减少。与野生型种子相比,Ateh1 种子在渗透胁迫条件下发芽延迟,种子种皮对四唑红的通透性增加。这项工作报道了植物 EH 的生理作用,并将 AtEH1 鉴定为参与角质合成的复杂机制的新成员。