{"title":"Identifying rubber-related genes through developing a sense/antisense RNA expression mutant library of Taraxacum kok-saghyz Rodin.","authors":"Xiuli Fan, Qingwen Chen, Lianlian Hu, Chunyan Hai, Zepeng Hu, Junhui Zhang, Liquan Kou, Guodong Wang, Xiaoguang Song, Hong Yu, Xia Xu, Jiayang Li","doi":"10.1111/jipb.13969","DOIUrl":null,"url":null,"abstract":"<p><p>Taraxacum kok-saghyz Rodin (TKS) is a promising alternative crop source for producing high-quality natural rubber (NR) and has become an ideal model plant for studying NR biosynthesis, regulation mechanisms, and production. So far, only a very limited number of functional genes related to NR biosynthesis have been identified in TKS. To achieve a systematic identification of its novel functional genes, we developed a mutant system denoted sense/antisense RNA expression (SARE) and have generated more than 8,000 transgenic TKS plants. A series of mutants with altered phenotypes, particularly changes in NR contents, were identified. To evaluate the efficiency of this library, we chose one mutant, c112, which exhibits a significant increase in NR content, for in-depth characterization. The c112 mutant arose from the sense insertion of a dormancy-associated gene1 (DRM1)/auxin repressed protein (ARP) gene, which we named high natural rubber content1 (HRC1). In the c112 mutant, the concentrations of NR precursors isopentenyl pyrophosphate and dimethylallyl diphosphate decreased, while geranylgeranyl diphosphate increased, suggesting that HRC1 regulates metabolic flux in NR biosynthesis. In summary, the developed TKS SARE mutant library provides valuable genetic resources for identifying key functional genes to accelerate the domestication of TKS from wild species to economic crops through molecular breeding.</p>","PeriodicalId":195,"journal":{"name":"Journal of Integrative Plant Biology","volume":" ","pages":""},"PeriodicalIF":9.3000,"publicationDate":"2025-07-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Integrative Plant Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/jipb.13969","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Taraxacum kok-saghyz Rodin (TKS) is a promising alternative crop source for producing high-quality natural rubber (NR) and has become an ideal model plant for studying NR biosynthesis, regulation mechanisms, and production. So far, only a very limited number of functional genes related to NR biosynthesis have been identified in TKS. To achieve a systematic identification of its novel functional genes, we developed a mutant system denoted sense/antisense RNA expression (SARE) and have generated more than 8,000 transgenic TKS plants. A series of mutants with altered phenotypes, particularly changes in NR contents, were identified. To evaluate the efficiency of this library, we chose one mutant, c112, which exhibits a significant increase in NR content, for in-depth characterization. The c112 mutant arose from the sense insertion of a dormancy-associated gene1 (DRM1)/auxin repressed protein (ARP) gene, which we named high natural rubber content1 (HRC1). In the c112 mutant, the concentrations of NR precursors isopentenyl pyrophosphate and dimethylallyl diphosphate decreased, while geranylgeranyl diphosphate increased, suggesting that HRC1 regulates metabolic flux in NR biosynthesis. In summary, the developed TKS SARE mutant library provides valuable genetic resources for identifying key functional genes to accelerate the domestication of TKS from wild species to economic crops through molecular breeding.
期刊介绍:
Journal of Integrative Plant Biology is a leading academic journal reporting on the latest discoveries in plant biology.Enjoy the latest news and developments in the field, understand new and improved methods and research tools, and explore basic biological questions through reproducible experimental design, using genetic, biochemical, cell and molecular biological methods, and statistical analyses.