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RNAi 机制调控参与毛霉目毒力的新核酸外切酶基因。

The RNAi Mechanism Regulates a New Exonuclease Gene Involved in the Virulence of Mucorales.

机构信息

Departmento de Genética y Microbiología, Facultad de Biología, Universidad de Murcia, 30100 Murcia, Spain.

出版信息

Int J Mol Sci. 2021 Feb 25;22(5):2282. doi: 10.3390/ijms22052282.

Abstract

Mucormycosis is a lethal disease caused by Mucorales, which are emerging as human causes that explain the high mortality for this disease. Consequently, the research community is searching for virulence determinants that could be repurposed as targets to develop new treatments against mucormycosis. Our work explores an RNA interference (RNAi)-based approach to find targets involved in the virulence of Mucorales. A transcriptomewide analysis compared sRNAs and their target mRNAs in two different pathotypes, virulent and avirulent, generating a list of 75 loci selected by their differential sRNA accumulation in these strains. As a proof of concept and validity, an experimental approach characterized two loci showing opposite behavior, confirming that RNAi activity causes their differential expression in the two pathotypes. We generated deletion mutants for two loci and a knockin-strain overexpressing for one of these loci. Their functional analysis in murine virulence assays identified the gene a putative DEDDy exonuclease with RNase domains, as an essential factor for virulence. The identification of showed the potential of our approach to discover virulence factors not only in Mucorales but also in any other fungal model with an active RNAi machinery. More importantly, it adds a new layer to the biological processes controlled by RNAi in , confirming that the Dicer-dependent RNAi pathway can silence gene expression to promote virulence.

摘要

毛霉病是一种由毛霉目真菌引起的致命疾病,这些真菌正逐渐成为导致该疾病高死亡率的人类病原体。因此,研究界正在寻找毒力决定因素,这些因素可能被重新用作开发抗毛霉病新疗法的靶点。我们的工作探索了一种基于 RNA 干扰 (RNAi) 的方法来寻找与毛霉目真菌毒力相关的靶点。对两种不同的病原型(毒力型和非毒力型)的 sRNA 和其靶 mRNA 进行了转录组分析,生成了一份由这些菌株中差异 sRNA 积累选择的 75 个基因座的列表。作为概念验证和有效性的证明,一种实验方法对两个表现出相反行为的基因座进行了特征描述,证实了 RNAi 活性导致它们在两种病原型中的差异表达。我们生成了两个基因座的缺失突变体和一个过表达这些基因座之一的敲入菌株。在小鼠毒力测定中的功能分析鉴定了一个假定的 DEDDy 外切核酸酶,该酶具有 RNA 酶结构域,是毒力的必需因素。对 的鉴定表明,我们的方法不仅可以在毛霉目中发现毒力因子,而且可以在任何具有活跃 RNAi 机制的其他真菌模型中发现毒力因子。更重要的是,它为 RNAi 控制的生物学过程增加了一个新的层面,证实了 Dicer 依赖性 RNAi 途径可以沉默基因表达以促进毒力。

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