Tossolini Ileana, Manavella Pablo Andrés, Arce Agustín Lucas
Instituto de Agrobiotecnología del Litoral (CONICET-UNL), 3000 Santa Fe, Argentina.
Instituto de Investigación y Desarrollo en Bioingeniería y Bioinformática (IBB-CONICET). Facultad de Ingeniería, Universidad Nacional de Entre Ríos, 3100 Oro Verde, Argentina.
Methods Mol Biol. 2025;2900:91-106. doi: 10.1007/978-1-0716-4398-3_5.
MicroRNAs are small regulatory RNAs of 20-24 nt, which guide the RNA-induced silencing complex to silence several genes post-transcriptionally. Plant miRNA biogenesis involves many steps, including their 2'-O-methylation at their 3' end, which protects them from degradation. In addition, there are two other types of modifications involved in miRNA turnover: trimming and tailing. This method describes a bioinformatics analysis procedure to evaluate miRNA trimming and tailing from sRNA-Seq data. The pipeline includes the steps required to download the raw data from public repositories and important considerations to analyze a large number of samples. It starts from the raw sequencing reads and involves 3' adaptor removal, quality filtering, alignment to a masked reference genome to discard unwanted reads, and the assessment of the degree of trimming and tailing for each miRNA. Finally, an index for these modifications is calculated, and the results are evaluated graphically and statistically. In conclusion, this scalable pipeline allows researchers to begin with raw data from various sRNA-seq studies and progress to meaningful results and visual representations.
微小RNA是一类长度为20 - 24个核苷酸的小调控RNA,它们引导RNA诱导沉默复合体在转录后使多个基因沉默。植物微小RNA的生物发生涉及多个步骤,包括其3'端的2'-O-甲基化,这可保护它们不被降解。此外,微小RNA周转还涉及另外两种类型的修饰:修剪和加尾。本方法描述了一种生物信息学分析程序,用于从sRNA测序数据评估微小RNA的修剪和加尾情况。该流程包括从公共数据库下载原始数据所需的步骤以及分析大量样本的重要注意事项。它从原始测序读数开始,涉及去除3'接头、质量过滤、与经过掩码处理的参考基因组比对以丢弃不需要的读数,以及评估每个微小RNA的修剪和加尾程度。最后,计算这些修饰的指数,并以图形和统计方式评估结果。总之,这种可扩展的流程使研究人员能够从各种sRNA测序研究的原始数据开始,进而获得有意义的结果和可视化表示。