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纯化后的植物ABC转运蛋白NtPDR1的活性受到参与组成型防御和诱导型防御的二萜类化合物和倍半萜类化合物的刺激。

Activity of the purified plant ABC transporter NtPDR1 is stimulated by diterpenes and sesquiterpenes involved in constitutive and induced defenses.

作者信息

Pierman Baptiste, Toussaint Frédéric, Bertin Aurélie, Lévy Daniel, Smargiasso Nicolas, De Pauw Edwin, Boutry Marc

机构信息

From the Institut des Sciences de la Vie, Université catholique de Louvain, B-1348 Louvain-la-Neuve, Belgium.

the Laboratoire Physico Chimie Curie, Institut Curie, Paris Sciences et Lettres Research University, CNRS UMR168, and Sorbonne Universités, Université Pierre et Marie Curie Paris 06, 75005 Paris, France, and.

出版信息

J Biol Chem. 2017 Nov 24;292(47):19491-19502. doi: 10.1074/jbc.M117.811935. Epub 2017 Sep 29.

Abstract

Within the plant ATP-binding cassette transporter family, pleiotropic drug resistance (PDR) transporters play essential functions, such as in hormone transport or defense against biotic and abiotic stresses. NtPDR1 from has been shown to be involved in the constitutive defense against pathogens through the secretion of toxic cyclic diterpenes, such as the antimicrobial substrates cembrene and sclareol from the leaf hairs (trichomes). However, direct evidence of an interaction between NtPDR1 and terpenes is lacking. Here, we stably expressed NtPDR1 in BY-2 suspension cells. NtPDR1 was purified as an active monomer glycosylated at a single site in the third external loop. NtPDR1 reconstitution in proteoliposomes stimulated its basal ATPase activity from 21 to 38 nmol of P·mg·min, and ATPase activity was further stimulated by the NtPDR1 substrates cembrene and sclareol, providing direct evidence of an interaction between NtPDR1 and its two substrates. Interestingly, NtPDR1 was also stimulated by capsidiol, a sesquiterpene produced by upon pathogen attack. We also monitored the transcriptional activity from the promoter with a reporter gene and found that, although expression was limited to trichomes under normal conditions, addition of methyl jasmonate, a biotic stress hormone, induced expression in all leaf tissues. This finding indicated that NtPDR1 is involved not only in constitutive but also in induced plant defenses. In conclusion, we provide direct evidence of an interaction between the NtPDR1 transporter and its substrates and that NtPDR1 transports compounds involved in both constitutive (diterpenes) and induced (sesquiterpenes) plant defenses.

摘要

在植物ATP结合盒转运蛋白家族中,多药耐药性(PDR)转运蛋白发挥着重要功能,例如在激素运输或抵御生物和非生物胁迫方面。已证明来自烟草的NtPDR1通过分泌有毒的环状二萜类化合物参与对病原体的组成性防御,例如从叶毛(表皮毛)分泌抗菌底物西松烯和香紫苏醇。然而,缺乏NtPDR1与萜类化合物之间相互作用的直接证据。在这里,我们在烟草BY-2悬浮细胞中稳定表达了NtPDR1。NtPDR1被纯化,其作为一个在第三个外环单一位点糖基化的活性单体。将NtPDR1重组到蛋白脂质体中可将其基础ATP酶活性从21提高到38 nmol Pi·mg-1·min-1,并且ATP酶活性被NtPDR1底物西松烯和香紫苏醇进一步激活,这为NtPDR1与其两种底物之间的相互作用提供了直接证据。有趣的是,NtPDR1也被辣椒素激活,辣椒素是烟草在病原体攻击时产生的一种倍半萜。我们还用报告基因监测了来自NtPDR1启动子的转录活性,发现尽管在正常条件下NtPDR1的表达仅限于表皮毛,但添加生物胁迫激素茉莉酸甲酯可诱导其在所有叶片组织中表达。这一发现表明NtPDR1不仅参与组成性防御,还参与诱导性植物防御。总之,我们提供了NtPDR1转运蛋白与其底物之间相互作用的直接证据,并且NtPDR1转运参与组成性(二萜类)和诱导性(倍半萜类)植物防御的化合物。

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