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从寄生模式线虫巴西日圆线虫和旋毛虫的细胞外囊泡中分离和分析 microRNAs。

Isolation and Analysis of MicroRNAs from Extracellular Vesicles of the Parasitic Model Nematodes Nippostrongylus brasiliensis and Trichuris muris.

机构信息

Institute of Parasitology, University of Zurich, Zurich, Switzerland.

出版信息

Methods Mol Biol. 2021;2369:319-332. doi: 10.1007/978-1-0716-1681-9_17.

Abstract

The identification, detection, and use of small RNA species have rapidly gained interest-especially to study parasite-host interactions. Parasite-to-host communication is contributed by small secreted extracellular vesicle (EV)-derived nucleic acid species. In particular, microRNAs (miRNAs) and small interfering RNAs can regulate the host response by targeting cells at both transcriptional and posttranscriptional levels. Here, modified protocols for density gradient purification of EVs from nematodes and the subsequent extraction of EV-derived small RNAs using commercially available reagents and kits are provided with a special focus on basic background information. Further, considerations for Next-Generation Sequencing using the Illumina NextSeq500 sequencing technology (kit-based library preparation, small RNA sequencing, and miRNA sequence analysis pipelines using the miRDeep2 package) are introduced.

摘要

小 RNA 种类的鉴定、检测和利用已经迅速引起了人们的兴趣——尤其是在研究寄生虫-宿主相互作用方面。寄生虫到宿主的通讯是由小的分泌型细胞外囊泡 (EV)衍生的核酸种类贡献的。特别是 microRNAs (miRNAs) 和 small interfering RNAs 可以通过靶向转录和转录后水平的细胞来调节宿主反应。在这里,提供了从线虫中密度梯度纯化 EV 并随后使用市售试剂和试剂盒提取 EV 衍生的小 RNA 的改良方案,特别强调了基本背景信息。此外,还介绍了使用 Illumina NextSeq500 测序技术 (基于试剂盒的文库制备、小 RNA 测序和使用 miRDeep2 包的 miRNA 序列分析管道) 进行下一代测序的注意事项。

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