Maximiliano S. Beckel, Abril San Martín, Sabrina E. Sánchez, Danelle K. Seymour, María José de Leone, Daniel A. Careno, Santiago Mora‐García, Detlef Weigel, Marcelo J. Yanovsky, Ariel Chernomoretz
{"title":"Arabidopsis PRMT5 buffers pre‐mRNA splicing and development against genetic variation in donor splice sites","authors":"Maximiliano S. Beckel, Abril San Martín, Sabrina E. Sánchez, Danelle K. Seymour, María José de Leone, Daniel A. Careno, Santiago Mora‐García, Detlef Weigel, Marcelo J. Yanovsky, Ariel Chernomoretz","doi":"10.1111/nph.70293","DOIUrl":null,"url":null,"abstract":"Summary<jats:list list-type=\"bullet\"> <jats:list-item>Genetic variation at splice site signals significantly influences alternative splicing, leading to transcriptomic and proteomic diversity that enhances phenotypic plasticity and adaptation. However, novel splice variants can negatively impact gene expression and developmental stability. Canalization–the ability of an organism to maintain a consistent phenotype despite genetic or environmental variations–helps balance the effects of genetic variation on development and evolution.</jats:list-item> <jats:list-item>Protein arginine methyltransferase 5 (PRMT5) is a key splicing regulator in plants and animals. Most splicing changes in <jats:italic>prmt5</jats:italic> mutants are linked to weak donor splice sites, suggesting that PRMT5 may buffer splicing against genetic variation.</jats:list-item> <jats:list-item>We examined PRMT5′s effects on splicing and development in two genetically divergent <jats:italic>Arabidopsis thaliana</jats:italic> accessions with different single nucleotide polymorphisms affecting donor splice sites. We found that PRMT5 inactivation significantly increased splicing and phenotypic differences between the accessions.</jats:list-item> <jats:list-item>Our findings suggest that PRMT5 contributes to canalization, mitigating the impact of splice site polymorphisms and facilitating the evolution of adaptive splicing patterns.</jats:list-item> </jats:list>","PeriodicalId":214,"journal":{"name":"New Phytologist","volume":"100 1","pages":""},"PeriodicalIF":8.3000,"publicationDate":"2025-06-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Phytologist","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/nph.70293","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
SummaryGenetic variation at splice site signals significantly influences alternative splicing, leading to transcriptomic and proteomic diversity that enhances phenotypic plasticity and adaptation. However, novel splice variants can negatively impact gene expression and developmental stability. Canalization–the ability of an organism to maintain a consistent phenotype despite genetic or environmental variations–helps balance the effects of genetic variation on development and evolution.Protein arginine methyltransferase 5 (PRMT5) is a key splicing regulator in plants and animals. Most splicing changes in prmt5 mutants are linked to weak donor splice sites, suggesting that PRMT5 may buffer splicing against genetic variation.We examined PRMT5′s effects on splicing and development in two genetically divergent Arabidopsis thaliana accessions with different single nucleotide polymorphisms affecting donor splice sites. We found that PRMT5 inactivation significantly increased splicing and phenotypic differences between the accessions.Our findings suggest that PRMT5 contributes to canalization, mitigating the impact of splice site polymorphisms and facilitating the evolution of adaptive splicing patterns.
期刊介绍:
New Phytologist is an international electronic journal published 24 times a year. It is owned by the New Phytologist Foundation, a non-profit-making charitable organization dedicated to promoting plant science. The journal publishes excellent, novel, rigorous, and timely research and scholarship in plant science and its applications. The articles cover topics in five sections: Physiology & Development, Environment, Interaction, Evolution, and Transformative Plant Biotechnology. These sections encompass intracellular processes, global environmental change, and encourage cross-disciplinary approaches. The journal recognizes the use of techniques from molecular and cell biology, functional genomics, modeling, and system-based approaches in plant science. Abstracting and Indexing Information for New Phytologist includes Academic Search, AgBiotech News & Information, Agroforestry Abstracts, Biochemistry & Biophysics Citation Index, Botanical Pesticides, CAB Abstracts®, Environment Index, Global Health, and Plant Breeding Abstracts, and others.