Thao Minh Viet Nguyen, Dinh Thi Tran, Clara I Mata, Bram Van de Poel, Bart M Nicolaï, Maarten L A T M Hertog
{"title":"Gene expression driving ethylene biosynthesis and signaling pathways in ripening tomato fruit; a kinetic modelling approach.","authors":"Thao Minh Viet Nguyen, Dinh Thi Tran, Clara I Mata, Bram Van de Poel, Bart M Nicolaï, Maarten L A T M Hertog","doi":"10.1093/jxb/eraf055","DOIUrl":null,"url":null,"abstract":"<p><p>Ethylene biosynthesis and signaling are pivotal pathways in various plant aging processes, including fruit ripening. Kinetic models can be used to better understand metabolic pathways, but modeling of the ethylene-related pathways is limited and the link between these pathways remains unsolved. A transcriptomics-based kinetic model was developed, consisting of ordinary differential equations describing ethylene biosynthesis and signaling pathways in tomato during fruit development and ripening, both on- and off-vine. This model was calibrated against a large volume of transcriptomic, proteomic and metabolic data during on-vine fruit development and ripening of tomato fruit grown in winter and summer. The model was validated using data on off-vine ripening of mature green harvested fruit grown in the same seasons. The ethylene biosynthesis pathway under different conditions appeared to be largely driven by gene expression levels. The ethylene-regulation of fruit ripening of a heat tolerant tomato grown in different seasons is identical but with quantitative differences at the targeted omics levels. This is reflected by some of the same parameters with distinct values for summer and winter fruit. The current model is the first attempt to model the ethylene signaling pathway starting from gene expression, the various protein - protein interactions, including the link with ethylene production, internal ethylene levels and the binding to its receptors.</p>","PeriodicalId":15820,"journal":{"name":"Journal of Experimental Botany","volume":" ","pages":""},"PeriodicalIF":5.6000,"publicationDate":"2025-02-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Experimental Botany","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/jxb/eraf055","RegionNum":2,"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
Ethylene biosynthesis and signaling are pivotal pathways in various plant aging processes, including fruit ripening. Kinetic models can be used to better understand metabolic pathways, but modeling of the ethylene-related pathways is limited and the link between these pathways remains unsolved. A transcriptomics-based kinetic model was developed, consisting of ordinary differential equations describing ethylene biosynthesis and signaling pathways in tomato during fruit development and ripening, both on- and off-vine. This model was calibrated against a large volume of transcriptomic, proteomic and metabolic data during on-vine fruit development and ripening of tomato fruit grown in winter and summer. The model was validated using data on off-vine ripening of mature green harvested fruit grown in the same seasons. The ethylene biosynthesis pathway under different conditions appeared to be largely driven by gene expression levels. The ethylene-regulation of fruit ripening of a heat tolerant tomato grown in different seasons is identical but with quantitative differences at the targeted omics levels. This is reflected by some of the same parameters with distinct values for summer and winter fruit. The current model is the first attempt to model the ethylene signaling pathway starting from gene expression, the various protein - protein interactions, including the link with ethylene production, internal ethylene levels and the binding to its receptors.
期刊介绍:
The Journal of Experimental Botany publishes high-quality primary research and review papers in the plant sciences. These papers cover a range of disciplines from molecular and cellular physiology and biochemistry through whole plant physiology to community physiology.
Full-length primary papers should contribute to our understanding of how plants develop and function, and should provide new insights into biological processes. The journal will not publish purely descriptive papers or papers that report a well-known process in a species in which the process has not been identified previously. Articles should be concise and generally limited to 10 printed pages.