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An Efficient Method for the Extraction of High-Quality Fungal Total RNA to Study the Mycosphaerella fijiensis-Musa spp. Interaction

机译:一种高效的高质量真菌总RNA提取方法,用于研究斐济支原体-Musa spp。相互作用

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摘要

Efficient RNA isolation is a prerequisite for gene expression studies and it has an increasingly important role in the study of plant-fungal pathogen interactions. However, RNA isolation is difficult in filamentous fungi. These organisms are notorious for their rigid cell walls and the presence of high levels of carbohydrates, excreted from the fungal cells during submerged growth, which interferes with the extraction procedures. Although many commercial kits are already available for RNA isolation, they do not provide, in most cases, enough amount of pure RNA to be used in upstream applications. In the present work, we propose an easy and efficient protocol for isolating total RNA from the filamentous fungus Mycosphaerella fijiensis, the most important foliar pathogen of Musa spp. varieties worldwide. In addition, we applied the proposed protocol to the isolation of total RNA from banana leaves infected with the pathogen. Our methodology was developed based on the SDS method with modifications including a carbohydrate precipitation step. The protocol resulted in high-quality total RNA, from fungal mycelium grown in PDB medium and infected banana leaves, suitable for further molecular studies. The proposed methodology is also applicable to the ascomycete fungus Passalora fulva (syn. Cladosporum fulvum).
机译:高效的RNA分离是进行基因表达研究的先决条件,并且在植物-真菌病原体相互作用的研究中具有越来越重要的作用。但是,丝状真菌很难分离RNA。这些生物以其坚硬的细胞壁和淹没生长过程中从真菌细胞中排出的高水平碳水化合物的存在而臭名昭著,这干扰了提取过程。尽管已经有许多商业试剂盒可用于RNA分离,但在大多数情况下,它们不能提供足够数量的纯RNA用于上游应用。在目前的工作中,我们提出了一种简单有效的方案,用于从丝状真菌斐济支原体(Muspha spp的最重要的叶病原体)中分离总RNA。世界各地的品种。此外,我们将拟议的方案应用于从感染病原体的香蕉叶中分离总RNA。我们的方法是根据SDS方法开发的,并进行了修改,包括碳水化合物沉淀步骤。该方案从PDB培养基中生长的真菌菌丝体和受感染的香蕉叶中产生了高质量的总RNA,适用于进一步的分子研究。所提出的方法还适用于子囊真菌Passalora fulva(Syn。Cladosporum fulvum)。

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