{"title":"Characterization of <i>trans</i>-spliced chimeric RNAs: insights into the mechanism of <i>trans</i>-splicing.","authors":"Rui Yokomori, Takehiro G Kusakabe, Kenta Nakai","doi":"10.1093/nargab/lqae067","DOIUrl":null,"url":null,"abstract":"<p><p><i>Trans</i>-splicing is a post-transcriptional processing event that joins exons from separate RNAs to produce a chimeric RNA. However, the detailed mechanism of <i>trans</i>-splicing remains poorly understood. Here, we characterize <i>trans</i>-spliced genes and provide insights into the mechanism of <i>trans</i>-splicing in the tunicate <i>Ciona</i>. Tunicates are the closest invertebrates to humans, and their genes frequently undergo <i>trans</i>-splicing. Our analysis revealed that, in genes that give rise to both <i>trans</i>-spliced and non-<i>trans</i>-spliced messenger RNAs, <i>trans</i>-splice acceptor sites were preferentially located at the first functional acceptor site, and their paired donor sites were weak in both <i>Ciona</i> and humans. Additionally, we found that <i>Ciona trans</i>-spliced genes had GU- and AU-rich 5' transcribed regions. Our data and findings not only are useful for <i>Ciona</i> research community, but may also aid in a better understanding of the <i>trans</i>-splicing mechanism, potentially advancing the development of gene therapy based on <i>trans</i>-splicing.</p>","PeriodicalId":33994,"journal":{"name":"NAR Genomics and Bioinformatics","volume":"6 2","pages":"lqae067"},"PeriodicalIF":4.0000,"publicationDate":"2024-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11155486/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"NAR Genomics and Bioinformatics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/nargab/lqae067","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/6/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0
Abstract
Trans-splicing is a post-transcriptional processing event that joins exons from separate RNAs to produce a chimeric RNA. However, the detailed mechanism of trans-splicing remains poorly understood. Here, we characterize trans-spliced genes and provide insights into the mechanism of trans-splicing in the tunicate Ciona. Tunicates are the closest invertebrates to humans, and their genes frequently undergo trans-splicing. Our analysis revealed that, in genes that give rise to both trans-spliced and non-trans-spliced messenger RNAs, trans-splice acceptor sites were preferentially located at the first functional acceptor site, and their paired donor sites were weak in both Ciona and humans. Additionally, we found that Ciona trans-spliced genes had GU- and AU-rich 5' transcribed regions. Our data and findings not only are useful for Ciona research community, but may also aid in a better understanding of the trans-splicing mechanism, potentially advancing the development of gene therapy based on trans-splicing.