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分析新的小RNA序列。

Profiling New Small RNA Sequences.

作者信息

Tsuzuki Masayuki, Watanabe Yuichiro

机构信息

Department of Life Sciences, Graduate School of Arts and Sciences, The University of Tokyo, Komaba 3-8-1, Meguro, Tokyo, 153-8902, Japan.

出版信息

Methods Mol Biol. 2017;1456:177-188. doi: 10.1007/978-1-4899-7708-3_14.

Abstract

Small RNAs are key molecules in RNA silencing pathways that exert the sequence-specific regulation of gene expression and chromatin modifications in many eukaryotes. In plants, endogenous small RNAs, including microRNAs (miRNAs), trans-acting short interfering RNAs (tasiRNAs), and heterochromatic siRNAs (hc-siRNAs), play an important role in switching or orchestrating biological processes during the development and at the onset of stress responses. These endogenous and exogenous small RNAs are mainly 20-24 nucleotides in length. In addition, viral genome-derived siRNAs of similar lengths are produced during viral infection, and they exhibit anti-viral defense activity in RNA silencing pathway.Here, we introduce a method to isolate and characterize small RNA molecules possibly applicable to a wide range of plant resources and tissues. After purification from total RNAs, small RNAs were subjected to Illumina sequencing analysis using compatible reagents kits. Following the sample preparation protocol, small RNAs are ligated first at the 3'- and then at the 5'-end to the respective RNA adapters followed by reverse transcription with a set of primers to produce cDNAs with Index sequences at ends. After PCR amplification, cDNAs are subjected (after gel purification) to RNA-seq analysis. This method could be applied to isolate small RNAs from different sources and characterize small RNA profiles to compare different sets of samples, e.g., wild-type and mutant plants, plants under different stress environments, and virus-infected plants because the starting RNA material is free of contaminated starch or similar material which would block further analysis.

摘要

小RNA是RNA沉默途径中的关键分子,在许多真核生物中发挥基因表达的序列特异性调控和染色质修饰作用。在植物中,内源性小RNA,包括微小RNA(miRNA)、反式作用小干扰RNA(tasiRNA)和异染色质小干扰RNA(hc-siRNA),在发育过程和应激反应开始时,在切换或协调生物学过程中发挥重要作用。这些内源性和外源性小RNA的长度主要为20 - 24个核苷酸。此外,在病毒感染期间会产生长度相似的病毒基因组衍生的小干扰RNA,它们在RNA沉默途径中表现出抗病毒防御活性。在这里,我们介绍一种分离和鉴定小RNA分子的方法,该方法可能适用于广泛的植物资源和组织。从小RNA从总RNA中纯化后,使用兼容的试剂试剂盒对其进行Illumina测序分析。按照样品制备方案,小RNA首先在3'端连接,然后在5'端连接到各自的RNA接头,随后用一组引物进行逆转录,以产生末端带有索引序列的cDNA。PCR扩增后,对cDNA(经过凝胶纯化)进行RNA测序分析。该方法可用于从不同来源分离小RNA,并鉴定小RNA谱以比较不同组的样品,例如野生型和突变型植物、处于不同应激环境下的植物以及病毒感染的植物,因为起始RNA材料不含会阻碍进一步分析的污染淀粉或类似物质。

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