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结合基因功能分析的小RNA谱揭示了小麦-病原菌系统中缺乏跨界RNA干扰的证据。

sRNA Profiling Combined With Gene Function Analysis Reveals a Lack of Evidence for Cross-Kingdom RNAi in the Wheat - Pathosystem.

作者信息

Kettles Graeme J, Hofinger Bernhard J, Hu Pingsha, Bayon Carlos, Rudd Jason J, Balmer Dirk, Courbot Mikael, Hammond-Kosack Kim E, Scalliet Gabriel, Kanyuka Kostya

机构信息

Biointeractions and Crop Protection, Rothamsted Research, Harpenden, United Kingdom.

Syngenta Biotechnology, Inc., Research Triangle Park, NC, United States.

出版信息

Front Plant Sci. 2019 Jul 4;10:892. doi: 10.3389/fpls.2019.00892. eCollection 2019.

Abstract

Cross-kingdom small RNA (sRNA) silencing has recently emerged as a mechanism facilitating fungal colonization and disease development. Here we characterized RNAi pathways in , a major fungal pathogen of wheat, and assessed their contribution to pathogenesis. Computational analysis of fungal sRNA and host mRNA sequencing datasets was used to define the global sRNA populations in and predict their mRNA targets in wheat. 389 -induced sRNA loci were identified. sRNAs generated from some of these loci were predicted to target wheat mRNAs including those potentially involved in pathogen defense. However, molecular approaches failed to validate targeting of selected wheat mRNAs by fungal sRNAs. Mutant strains of carrying deletions of genes encoding key components of RNAi such as Dicer-like (DCL) and Argonaute (AGO) proteins were generated, and virulence bioassays suggested that these are dispensable for full infection of wheat. Nonetheless, our results did suggest the existence of non-canonical DCL-independent pathway(s) for sRNA biogenesis in . dsRNA targeting essential fungal genes applied or generated from an RNA virus vector in a procedure known as HIGS (Host-Induced Gene Silencing) was ineffective in preventing growth or disease. We also demonstrated that is incapable of dsRNA uptake. Collectively, our data suggest that RNAi approaches for gene function analyses in this fungal species and potentially also as a control measure may not be as effective as has been demonstrated for some other plant pathogenic fungi.

摘要

跨界小RNA(sRNA)沉默最近作为一种促进真菌定殖和疾病发展的机制出现。在这里,我们对小麦的主要真菌病原体——[具体真菌名称未给出]中的RNAi途径进行了表征,并评估了它们对致病作用的贡献。利用真菌sRNA和宿主mRNA测序数据集的计算分析来定义[具体真菌名称未给出]中的全局sRNA群体,并预测它们在小麦中的mRNA靶标。鉴定出389个由[具体真菌名称未给出]诱导的sRNA位点。预计其中一些位点产生的sRNA靶向小麦mRNA,包括那些可能参与病原体防御的mRNA。然而,分子方法未能验证真菌sRNA对选定小麦mRNA的靶向作用。构建了携带RNAi关键成分(如Dicer样(DCL)和AGO蛋白)编码基因缺失的[具体真菌名称未给出]突变菌株,毒力生物测定表明,这些基因对于小麦的完全感染是可有可无的。尽管如此,我们的结果确实表明在[具体真菌名称未给出]中存在不依赖DCL的非经典sRNA生物合成途径。在一种称为宿主诱导基因沉默(HIGS)的过程中,应用或由RNA病毒载体产生的靶向必需真菌基因的dsRNA在阻止[具体真菌名称未给出]生长或疾病方面无效。我们还证明[具体真菌名称未给出]不能摄取dsRNA。总体而言,我们的数据表明,在这种真菌物种中用于基因功能分析的RNAi方法以及潜在地作为一种控制措施可能不像对其他一些植物病原真菌所证明的那样有效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1cc6/6620828/92f347226e53/fpls-10-00892-g001.jpg

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