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转录组范围内鉴定番茄斑萎病毒衍生的小干扰 RNA 靶向的宿主基因。

Transcriptome-wide identification of host genes targeted by tomato spotted wilt virus-derived small interfering RNAs.

机构信息

Department of Plant Pathology, Washington State University, Pullman, WA 99164, USA.

Queensland Alliance for Agriculture and Food Innovation, University of Queensland, St. Lucia, QLD, Australia.

出版信息

Virus Res. 2017 Jun 15;238:13-23. doi: 10.1016/j.virusres.2017.05.014. Epub 2017 May 22.

Abstract

RNA silencing mechanism functions as a major defense against invading viruses. The caveat in the RNA silencing mechanism is that the effector small interfering RNAs (siRNAs) act on any RNA transcripts with sequence complementarity irrespective of target's origin. A subset of highly expressed viral small interfering RNAs (vsiRNAs) derived from the tomato spotted wilt virus (TSWV; Tospovirus: Bunyaviridae) genome was analyzed for their propensity to downregulate the tomato transcriptome. A total of 11898 putative target sites on tomato transcripts were found to exhibit a propensity for down regulation by TSWV-derived vsiRNAs. In total, 2450 unique vsiRNAs were found to have potential cross-reacting capability with the tomato transcriptome. VsiRNAs were found to potentially target a gamut of host genes involved in basal cellular activities including enzymes, transcription factors, membrane transporters, and cytoskeletal proteins. KEGG pathway annotation of targets revealed that the vsiRNAs were mapped to secondary metabolite biosynthesis, amino acids, starch and sucrose metabolism, and carbon and purine metabolism. Transcripts for protein processing, hormone signalling, and plant-pathogen interactions were the most likely targets from the genetic, environmental information processing, and organismal systems, respectively. qRT-PCR validation of target gene expression showed that none of the selected transcripts from tomato cv. Marglobe showed up regulation, and all were down regulated even upto 20 folds (high affinity glucose transporter). However, the expression levels of transcripts from cv. Red Defender revealed differential regulation as three among the target transcripts showed up regulation (Cc-nbs-lrr, resistance protein, AP2-like ethylene-responsive transcription factor, and heat stress transcription factor A3). Accumulation of tomato target mRNAs of corresponding length was proved in both tomato cultivars using 5' RACE analysis. The TSWV-tomato interaction at the sRNA interface points to the ability of tomato cultivars to overcome vsiRNA-mediated targeting of NBS-LRR class R genes. These results suggest the prevalence of vsiRNA-induced RNA silencing of host transcriptome, and the interactome scenario is the first report on the interaction between tospovirus genome-derived siRNAs and tomato transcripts, and provide a deeper understanding of the role of vsiRNAs in pathogenicity and in perturbing host machinery.

摘要

RNA 沉默机制是抵御入侵病毒的主要防御机制。然而,RNA 沉默机制存在一个缺陷,即效应小干扰 RNA(siRNA)会作用于任何具有序列互补性的 RNA 转录本,而不论其靶标来源如何。本研究分析了源自番茄斑萎病毒(TSWV;Tospovirus: Bunyaviridae)基因组的一组高度表达的病毒小干扰 RNA(vsiRNA),以研究其下调番茄转录组的倾向。在番茄转录本上发现了总共 11898 个潜在的靶标位点,这些靶标位点表现出被 TSWV 衍生的 vsiRNA 下调的倾向。总共发现了 2450 个独特的 vsiRNA 具有与番茄转录组交叉反应的潜在能力。vsiRNA 可能靶向一系列参与基础细胞活动的宿主基因,包括酶、转录因子、膜转运蛋白和细胞骨架蛋白。对靶标的 KEGG 途径注释表明,vsiRNA 被映射到次生代谢物生物合成、氨基酸、淀粉和蔗糖代谢以及碳和嘌呤代谢。从遗传、环境信息处理和生物体系统来看,蛋白质加工、激素信号和植物-病原体相互作用的转录本最有可能成为靶标。qRT-PCR 验证靶基因表达显示,Marglobe 番茄品系中没有选择的转录本上调,所有转录本均下调,甚至下调 20 倍(高亲和力葡萄糖转运蛋白)。然而,Red Defender 番茄品系的转录本表达水平显示出不同的调控方式,其中 3 个靶转录本上调(Cc-nbs-lrr、抗性蛋白、AP2 样乙烯响应转录因子和热应激转录因子 A3)。使用 5' RACE 分析证明了番茄中对应长度的番茄靶标 mRNA 的积累。在番茄与 TSWV 的相互作用中,siRNA 界面的靶标 mRNAs 指向番茄品种克服 vsiRNA 介导的 NBS-LRR 类 R 基因靶向的能力。这些结果表明,vsiRNA 诱导的宿主转录组 RNA 沉默普遍存在,互作组场景是首例报道的 Tospovirus 基因组衍生 siRNA 与番茄转录本之间的相互作用,并提供了对 vsiRNA 在致病性和扰乱宿主机制中的作用的更深入理解。

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