{"title":"反式拼接嵌合 RNA 的特征:反式拼接机制的启示。","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":"{\"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}","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}
Characterization of trans-spliced chimeric RNAs: insights into the mechanism of trans-splicing.
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.