University of Thessaly, Department of Biochemistry & Biotechnology, Larissa, Greece.
Hellenic Agricultural Organization Demeter, Institute of Industrial and Forage Crops, Larissa, Greece.
RNA Biol. 2023 Jan;20(1):20-30. doi: 10.1080/15476286.2022.2159158.
A growing body of evidence suggests that RNA interference (RNAi) plays a pivotal role in the communication between plants and pathogenic fungi, where a bi-directional trans-kingdom RNAi is established to the advantage of either the host or the pathogen. Similar mechanisms acting during plant association with non-pathogenic symbiotic microorganisms have been elusive to this date. To determine whether root endophytes can induce systemic RNAi responses to their host plants, we designed an experimental reporter-based system consisting of the root-restricted, beneficial fungal endophyte, strain K (FsK) and its host . Since not all fungi encode the RNAi machinery, we first needed to validate that FsK does so, by identifying its core RNAi enzymes (2 Dicer-like genes, 2 Argonautes and 4 RNA-dependent RNA polymerases) and by showing its susceptibility to RNAi upon exogenous application of double stranded RNAs (dsRNAs). Upon establishing this, we transformed FsK with a hairpin RNA (hpRNA) construct designed to target a reporter gene in its host . The hpRNA was processed by FsK RNAi machinery predominantly into 21-24-nt small RNAs that triggered RNA silencing but not DNA methylation in the fungal hyphae. Importantly, when the hpRNA-expressing FsK was used to inoculate , systemic RNA silencing and DNA methylation of the host reporter gene was recorded. Our data suggest that RNAi signals can be translocated by root endophytes to their hosts and can modulate gene expression during mutualism, which may be translated to beneficial phenotypes.
越来越多的证据表明,RNA 干扰(RNAi)在植物与病原真菌之间的通讯中起着关键作用,在这种通讯中建立了双向的跨领域 RNAi,有利于宿主或病原体。迄今为止,在植物与非致病性共生微生物的相互作用中,类似的机制还难以捉摸。为了确定根内生真菌是否能诱导宿主植物的系统性 RNAi 反应,我们设计了一个基于实验报告的系统,该系统由根限制的有益真菌内生菌 菌株 K(FsK)及其宿主 组成。由于并非所有真菌都编码 RNAi 机制,我们首先需要通过鉴定 FsK 的核心 RNAi 酶(2 个 Dicer 样基因、2 个 Argonautes 和 4 个 RNA 依赖性 RNA 聚合酶)并通过显示其对外源双链 RNA(dsRNA)的 RNAi 敏感性来验证这一点。在建立了这一点之后,我们用针对其宿主报告基因的发夹 RNA(hpRNA)构建体转化了 FsK。hpRNA 主要被 FsK 的 RNAi 机制加工成 21-24 个核苷酸的小 RNA,触发了真菌菌丝中的 RNA 沉默但不触发 DNA 甲基化。重要的是,当表达 hpRNA 的 FsK 被用来接种 时,记录到了宿主报告基因的系统性 RNA 沉默和 DNA 甲基化。我们的数据表明,RNAi 信号可以被根内生菌转移到它们的宿主中,并在共生关系中调节基因表达,这可能转化为有益的表型。