Dalakouras Athanasios, Jarausch Wolfgang, Buchholz Guenther, Bassler Alexandra, Braun Mario, Manthey Thorsten, Krczal Gabi, Wassenegger Michael
RLP AgroScience GmbH, AlPlanta - Institute for Plant Research, Neustadt, Germany.
Institute of Plant Breeding and Genetic Resources ELGO-DEMETER, Thessaloniki, Greece.
Front Plant Sci. 2018 Aug 24;9:1253. doi: 10.3389/fpls.2018.01253. eCollection 2018.
Since its discovery, RNA interference has been widely used in crop protection. Recently, transgene-free procedures that were based on exogenous application of RNA molecules having the capacity to trigger RNAi have been reported. Yet, efficient delivery of such RNA molecules to plants and particularly to trees poses major technical challenges. Here, we describe simple methods for efficient delivery of hairpin RNAs (hpRNAs) and small interfering RNAs (siRNAs) to , , and that are based on trunk injection and/or petiole absorption. The applied RNA molecules were efficiently taken up and systemically transported. In apical leaves, the RNA was already detectable 1 day post-application (dpa) and could be detected at least up to 10 dpa, depending on the method of application. Confocal microscopy revealed that the uptaken and systemically transported RNA molecules were strictly restricted to the xylem and apoplast which may illustrate why the applied hpRNAs were not processed into siRNAs by plant DICER-LIKE (DCL) endonucleases. These innovative methods may have great impact in pest management against chewing and/or xylem sap-feeding vectors and eukaryotic pathogens that reside in the xylem.
自发现以来,RNA干扰已广泛应用于作物保护。最近,已报道了基于外源应用具有触发RNA干扰能力的RNA分子的无转基因程序。然而,将此类RNA分子有效递送至植物尤其是树木面临重大技术挑战。在此,我们描述了基于树干注射和/或叶柄吸收,将发夹RNA(hpRNA)和小干扰RNA(siRNA)有效递送至杨树、柳树和悬铃木的简单方法。所应用的RNA分子被有效吸收并进行系统运输。在顶端叶片中,施用后1天(dpa)即可检测到RNA,根据施用方法,至少在10 dpa时仍可检测到。共聚焦显微镜显示,吸收并系统运输的RNA分子严格局限于木质部和质外体,这可能解释了为何所应用的hpRNA未被植物类Dicer(DCL)核酸内切酶加工成siRNA。这些创新方法可能对防治咀嚼式和/或取食木质部汁液的媒介害虫以及寄生于木质部的真核病原体具有重大影响。