真菌的 sRNA 能抑制宿主植物的转录因子,促进丛枝菌根共生。

IF 9.4 1区 生物学 Q1 Agricultural and Biological Sciences New Phytologist Pub Date : 2024-11-18 DOI:10.1111/nph.20273
Alessandro Silvestri, William Conrad Ledford, Valentina Fiorilli, Cristina Votta, Alessia Scerna, Jacopo Tucconi, Antonio Mocchetti, Gianluca Grasso, Raffaella Balestrini, Hailing Jin, Ignacio Rubio-Somoza, Luisa Lanfranco
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引用次数: 0

摘要

跨域 RNA 干扰(ckRNAi)是一种种间交流机制,即小 RNA(sRNA)从一种生物体运输到另一种生物体;这些 sRNA 通过加载到宿主 AGO 蛋白中,反式抑制目标基因。在这项工作中,我们研究了丛枝菌根共生(AMS)中ckRNAi的发生。我们利用硅预测分析确定了来自AM真菌Rhizophagus irregularis的sRNA(Rir2216)及其推测的植物基因靶标--Medicago truncatula MtWRKY69转录因子。我们利用烟草中的异源共表达实验、5' RACE 反应和菌根中的 AGO1 免疫沉淀实验来确定 Rir2216-MtWRKY69 相互作用的特征。我们进一步分析了 MtWRKY69 的表达谱以及组成型和条件型 MtWRKY69 表达对 AMS 的贡献。我们发现,Rir2216 被加载到宿主植物 M. truncatula 的 AGO1 沉默复合体中,导致宿主目标转录本编码 MtWRKY69 转录因子被裂解。MtWRKY69在菌根的假根细胞中特异性下调,MtWRKY69表达水平的增加导致AM定殖水平的降低。我们的研究结果表明,由真菌 sRNA 介导的 MtWRKY69 沉默与 AMS 有关;因此,我们首次提出了 AMS 中真菌对植物 ckRNAi 的实验证据。
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A fungal sRNA silences a host plant transcription factor to promote arbuscular mycorrhizal symbiosis.

Cross-kingdom RNA interference (ckRNAi) is a mechanism of interspecies communication where small RNAs (sRNAs) are transported from one organism to another; these sRNAs silence target genes in trans by loading into host AGO proteins. In this work, we investigated the occurrence of ckRNAi in Arbuscular Mycorrhizal Symbiosis (AMS). We used an in silico prediction analysis to identify a sRNA (Rir2216) from the AM fungus Rhizophagus irregularis and its putative plant gene target, the Medicago truncatula MtWRKY69 transcription factor. Heterologous co-expression assays in Nicotiana benthamiana, 5' RACE reactions and AGO1-immunoprecipitation assays from mycorrhizal roots were used to characterize the Rir2216-MtWRKY69 interaction. We further analyzed MtWRKY69 expression profile and the contribution of constitutive and conditional MtWRKY69 expression to AMS. We show that Rir2216 is loaded into an AGO1 silencing complex from the host plant M. truncatula, leading to cleavage of a host target transcript encoding for the MtWRKY69 transcription factor. MtWRKY69 is specifically downregulated in arbusculated cells in mycorrhizal roots and increased levels of MtWRKY69 expression led to a reduced AM colonization level. Our results indicate that MtWRKY69 silencing, mediated by a fungal sRNA, is relevant for AMS; we thus present the first experimental evidence of fungus to plant ckRNAi in AMS.

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来源期刊
New Phytologist
New Phytologist PLANT SCIENCES-
CiteScore
17.60
自引率
5.30%
发文量
728
审稿时长
1 months
期刊介绍: New Phytologist is a leading publication that showcases exceptional and groundbreaking research in plant science and its practical applications. With a focus on five distinct sections - Physiology & Development, Environment, Interaction, Evolution, and Transformative Plant Biotechnology - the journal covers a wide array of topics ranging from cellular processes to the impact of global environmental changes. We encourage the use of interdisciplinary approaches, and our content is structured to reflect this. Our journal acknowledges the diverse techniques employed in plant science, including molecular and cell biology, functional genomics, modeling, and system-based approaches, across various subfields.
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