Godden Alice M, Rix Benjamin, Immler Simone
School of Biological Sciences, University of East Anglia, Norwich Research Park, Norwich, NR4 7TJ, UK.
Mob DNA. 2025 Jan 28;16(1):2. doi: 10.1186/s13100-025-00342-3.
Piwi-interacting RNAs (piRNA)s are non-coding small RNAs that post-transcriptionally affect gene expression and regulation. Through complementary seed region binding with transposable elements (TEs), piRNAs protect the genome from transposition. A tool to link piRNAs with complementary TE targets will improve our understanding of the role of piRNAs in genome maintenance and gene regulation. Existing tools such as TEsmall can process sRNA-seq datasets to produce differentially expressed piRNAs, and piRScan developed for nematodes can link piRNAs and TEs but it requires knowledge about the target region of interest and works backwards.
We developed FishPi to predict the pairings between piRNA and TEs for available genomes from zebrafish, medaka and tilapia, with full user customisation of parameters including orientation of piRNA, mismatches in the piRNA seed binding to TE and scored output lists of piRNA-TE matches. FishPi works with individual piRNAs or a list of piRNA sequences in fasta format. The software focuses on the piRNA-TE seed region and analyses reference TEs for piRNA complementarity. TE type is examined, counted and stored to a dictionary, with genomic loci recorded. Any updates to piRNA-TE binding rules can easily be incorporated by changing the seed-region options in the graphic user-interface. FishPi provides a graphic interface using tkinter for the user to input piRNA sequences to generate comprehensive reports on piRNA-TE interactions. FishPi can easily be adapted to genomes from other species and taxa opening the interpretation of piRNA functionality to a wide community.
Users will gain insight into genome mobility and FishPi will help further our understanding of the biological role of piRNAs and their interaction with TEs in a similar way that public databases have improved the access to and the understanding of the role of small RNAs.
Piwi相互作用RNA(piRNA)是一类非编码小RNA,可在转录后影响基因表达和调控。通过与转座元件(TE)的互补种子区域结合,piRNA可保护基因组免受转座作用的影响。一种将piRNA与互补TE靶标联系起来的工具将有助于我们更好地理解piRNA在基因组维持和基因调控中的作用。现有工具如TEsmall可以处理小RNA测序数据集以产生差异表达的piRNA,而针对线虫开发的piRScan可以将piRNA与TE联系起来,但它需要有关感兴趣靶区域的知识并且是反向工作的。
我们开发了FishPi,用于预测斑马鱼、青鳉和罗非鱼等可用基因组中piRNA与TE之间的配对,用户可以完全自定义参数,包括piRNA的方向、piRNA种子与TE结合中的错配以及piRNA-TE匹配的评分输出列表。FishPi适用于单个piRNA或以fasta格式列出的piRNA序列列表。该软件专注于piRNA-TE种子区域,并分析参考TE与piRNA的互补性。检查、计数并将TE类型存储到字典中,并记录基因组位点。通过更改图形用户界面中的种子区域选项,可以轻松纳入对piRNA-TE结合规则的任何更新。FishPi使用tkinter提供图形界面,供用户输入piRNA序列以生成有关piRNA-TE相互作用的综合报告。FishPi可以轻松适应其他物种和分类群的基因组,从而使广大群体能够解读piRNA的功能。
用户将深入了解基因组的流动性,FishPi将有助于进一步加深我们对piRNA生物学作用及其与TE相互作用的理解,就像公共数据库改善了对小RNA作用的获取和理解一样。