真菌 Fusarium fujikuroi 中的 RNAi 机制在合成介质中并不十分活跃,且与可转座元件有关

IF 3.6 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Javier Pardo-Medina, Tim A. Dahlmann, Minou Nowrousian, M. Carmen Limón, Javier Avalos
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引用次数: 0

摘要

小 RNAS(sRNA)参与了包括真菌在内的多种真核生物的 RNA 干扰(RNAi)调控机制。真菌 Fusarium fujikuroi 是研究次生代谢的模型,它含有一套完整的 RNAi 通路基因。我们利用 150 nt 以下的文库,通过高通量测序分析了在合成培养基中黑暗或光照 1 小时后生长的 F. fujikuroi 总 RNA 样本中 sRNA 的含量,涵盖了 sRNA 及其前体。为了进行比较,还与 Fusarium oxysporum 进行了平行分析。在这两个物种中,sRNA 读数显示,在预期大小的 RNA 样本中,5′尿嘧啶的比例较高,这表明存在真正的 sRNA,并通过预测软件鉴定出了假定的 miRNA 样 sRNA(milRNAS)。F. fujikuroi携带至少一个转录表达的Ty1/copia样逆转录转座元件,在其中的有义和反义DNA链中都发现了sRNA,而在F. oxysporum的skippy样元件中也有sRNA形成。在这些可移动元件中发现 sRNA 表明存在一种活跃的基于 sRNA 的 RNAi 途径。dcl2 是在测试条件下唯一有显著表达的 F. fujikuroi Dicer 基因,靶向删除 dcl2 并没有产生明显的表型或转录组变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The RNAi Machinery in the Fungus Fusarium fujikuroi Is Not Very Active in Synthetic Medium and Is Related to Transposable Elements
Small RNAS (sRNAs) participate in regulatory RNA interference (RNAi) mechanisms in a wide range of eukaryotic organisms, including fungi. The fungus Fusarium fujikuroi, a model for the study of secondary metabolism, contains a complete set of genes for RNAi pathways. We have analyzed by high-throughput sequencing the content of sRNAs in total RNA samples of F. fujikuroi grown in synthetic medium in the dark or after 1 h of illumination, using libraries below 150 nt, covering sRNAs and their precursors. For comparison, a parallel analysis with Fusarium oxysporum was carried out. The sRNA reads showed a higher proportion of 5′ uracil in the RNA samples of the expected sizes in both species, indicating the occurrence of genuine sRNAs, and putative miRNA-like sRNAs (milRNAS) were identified with prediction software. F. fujikuroi carries at least one transcriptionally expressed Ty1/copia-like retrotransposable element, in which sRNAs were found in both sense and antisense DNA strands, while in F. oxysporum skippy-like elements also show sRNA formation. The finding of sRNA in these mobile elements indicates an active sRNA-based RNAi pathway. Targeted deletion of dcl2, the only F. fujikuroi Dicer gene with significant expression under the conditions tested, did not produce appreciable phenotypic or transcriptomic alterations.
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来源期刊
Non-Coding RNA
Non-Coding RNA Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
6.70
自引率
4.70%
发文量
74
审稿时长
10 weeks
期刊介绍: Functional studies dealing with identification, structure-function relationships or biological activity of: small regulatory RNAs (miRNAs, siRNAs and piRNAs) associated with the RNA interference pathway small nuclear RNAs, small nucleolar and tRNAs derived small RNAs other types of small RNAs, such as those associated with splice junctions and transcription start sites long non-coding RNAs, including antisense RNAs, long ''intergenic'' RNAs, intronic RNAs and ''enhancer'' RNAs other classes of RNAs such as vault RNAs, scaRNAs, circular RNAs, 7SL RNAs, telomeric and centromeric RNAs regulatory functions of mRNAs and UTR-derived RNAs catalytic and allosteric (riboswitch) RNAs viral, transposon and repeat-derived RNAs bacterial regulatory RNAs, including CRISPR RNAS Analysis of RNA processing, RNA binding proteins, RNA signaling and RNA interaction pathways: DICER AGO, PIWI and PIWI-like proteins other classes of RNA binding and RNA transport proteins RNA interactions with chromatin-modifying complexes RNA interactions with DNA and other RNAs the role of RNA in the formation and function of specialized subnuclear organelles and other aspects of cell biology intercellular and intergenerational RNA signaling RNA processing structure-function relationships in RNA complexes RNA analyses, informatics, tools and technologies: transcriptomic analyses and technologies development of tools and technologies for RNA biology and therapeutics Translational studies involving long and short non-coding RNAs: identification of biomarkers development of new therapies involving microRNAs and other ncRNAs clinical studies involving microRNAs and other ncRNAs.
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