Abstract

Current bioinformatics workflows for PIWI-interacting RNA (piRNA) analysis focus primarily on germline-derived piRNAs and piRNA-clusters. Frequently, they suffer from outdated piRNA databases, questionable quantification methods, and lack of reproducibility. Often, pipelines specific to miRNA analysis are used for the piRNA research in silico. Furthermore, the absence of a well-established database for piRNA annotation, as for miRNA, leads to uniformity issues between studies and generates confusion for data analysts and biologists. For these reasons, we have developed WIND (Workflow for pIRNAs aNd beyonD), a bioinformatics workflow that addresses the crucial issue of piRNA annotation, thereby allowing a reliable analysis of small RNA sequencing data for the identification of piRNAs and other small non-coding RNAs (sncRNAs) that in the past have been incorrectly classified as piRNAs. WIND allows the creation of a comprehensive annotation track of sncRNAs combining information available in RNAcentral, with piRNA sequences from piRNABank, the first database dedicated to piRNA annotation. WIND was built with Docker containers for reproducibility and integrates widely used bioinformatics tools for sequence alignment and quantification. In addition, it includes Bioconductor packages for exploratory data and differential expression analysis. Moreover, WIND implements a "dual" approach for the evaluation of sncRNAs expression level quantifying the aligned reads to the annotated genome and carrying out an alignment-free transcript quantification using reads mapped to the transcriptome. Therefore, a broader range of piRNAs can be annotated, improving their quantification and easing the subsequent downstream analysis. WIND performance has been tested with several small RNA-seq datasets, demonstrating how our approach can be a useful and comprehensive resource to analyse piRNAs and other classes of sncRNAs.

Highlights

  • Advances in the field of Next-Generation Sequencing and big data analysis have led to the identification of several small non-coding RNA classes, some of which are still poorly characterised[1,2]

  • The GTF file was created as described in the Methods obtaining 155,143 different genomic locations corresponding to 43,973 sequences in human and 932,645 distinct genomic locations corresponding to 99,624 sequences in mouse for all small RNA types

  • We found that the PIWI-interacting RNA (piRNA) population identified in adult cardiac myocyte (aCM) represents 11% of all reads assigned to small RNAs, and the top 100 expressed molecules are listed in Supplementary Table 3 (Extended data)

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Summary

Introduction

Advances in the field of Next-Generation Sequencing and big data analysis have led to the identification of several small non-coding RNA (sncRNA) classes, some of which are still poorly characterised[1,2]. A subset of piRNAs present an adenosine bias at position 10, a feature indicating their biogenesis through the ping-pong cycle, a mechanism by which the cleavage of the target RNA is coupled with the production of a second population of target-specific piRNAs. A subset of piRNAs present an adenosine bias at position 10, a feature indicating their biogenesis through the ping-pong cycle, a mechanism by which the cleavage of the target RNA is coupled with the production of a second population of target-specific piRNAs They interact with PIWI proteins of the Argonaute (AGO) family, forming a silencing complex able to suppress transposable elements, regulate target’s gene expression at both epigenetic and post-transcriptional level and defend from viral infections[6]. These piRNA functions are well studied in the animal germline, in somatic cells, their role needs to be further elucidated. The abnormal expression of piRNAs has been associated with tumour initiation, progression, and metastasis formation and these molecules have shown the potential to be useful diagnostic tools and therapeutic targets as well as biomarkers for cancer prognosis[8]

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