The production and secretion of tRNA-derived RNA fragments in the corn smut fungus Ustilago maydis.

IF 2.1 Q3 MYCOLOGY Frontiers in fungal biology Pub Date : 2022-08-04 eCollection Date: 2022-01-01 DOI:10.3389/ffunb.2022.958798
Rei Yoshimoto, Fumiko Ishida, Miyuki Yamaguchi, Shigeyuki Tanaka
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引用次数: 3

Abstract

The biogenesis of small non-coding RNAs is a molecular event that contributes to cellular functions. The basidiomycete fungus Ustilago maydis is a biotrophic pathogen parasitizing maize. A hallmark of its genome structure is an absence of RNAi machinery including Dicer and Argonaute proteins, which are responsible for the production of small RNAs in other organisms. However, it remains unclear whether U. maydis produces small RNAs during fungal growth. Here we found that U. maydis cells accumulate approximately 20-30 nucleotides of small RNA fragments during growth in the axenic culture condition. The RNA-seq analysis of these fragments identified that these small RNAs are originated from tRNAs and 5.8S ribosomal RNA. Interestingly, majority of their sequences are generated from tRNAs responsible for asparagine, glutamine and glycine, suggesting a bias of origin. The cleavage of tRNAs mainly occurs at the position near anticodon-stem-loop. We generated the deletion mutants of two genes nuc1 and nuc2 encoding RNase T2, which is a candidate enzyme that cleaves tRNAs. The deletion mutants of two genes largely fail to accumulate tRNA-derived RNA fragments. Nuc1 and tRNA are co-localized at the tip of budding cells and tRNA fragment could be detected in culture supernatant. Our results suggest that specific tRNAs would be cleaved during secretory processes and tRNA fragments might have extracellular functions.

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玉米黑色素瘤菌中tRNA衍生RNA片段的产生和分泌。
小的非编码RNA的生物发生是一个有助于细胞功能的分子事件。担子菌(Ustilago maydis)是一种寄生在玉米上的生物营养性病原体。其基因组结构的一个标志是缺乏RNAi机制,包括Dicer和Argonaute蛋白,它们负责在其他生物体中产生小RNA。然而,目前尚不清楚五月花是否在真菌生长过程中产生小RNA。在这里,我们发现,在无菌培养条件下生长的过程中,玉米毒细胞积累了大约20-30个核苷酸的小RNA片段。对这些片段的RNA-seq分析表明,这些小RNA来源于tRNA和5.8S核糖体RNA。有趣的是,它们的大多数序列都是由负责天冬酰胺、谷氨酰胺和甘氨酸的tRNA产生的,这表明它们存在起源偏差。tRNA的切割主要发生在反密码子茎环附近的位置。我们产生了编码RNase T2的两个基因nuc1和nuc2的缺失突变体,RNase T2是一种切割tRNA的候选酶。两个基因的缺失突变体在很大程度上不能积累tRNA衍生的RNA片段。Nuc1和tRNA共同定位在出芽细胞的尖端,并且在培养上清液中可以检测到tRNA片段。我们的研究结果表明,特定的tRNA在分泌过程中会被切割,tRNA片段可能具有细胞外功能。
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2.70
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审稿时长
13 weeks
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