Wang Jianhui, Xu Rui, Guo Weiqing, Li Zhihong, Liu Dayu, Li Jingjing, Li Dagang, Chen Ying
{"title":"转录组学和代谢组学的整合分析表明,TT8的选择性剪接调节了采后血橙中温储存中花青素的生物合成。","authors":"Wang Jianhui, Xu Rui, Guo Weiqing, Li Zhihong, Liu Dayu, Li Jingjing, Li Dagang, Chen Ying","doi":"10.1007/s11103-025-01651-0","DOIUrl":null,"url":null,"abstract":"<p><p>To address the problem of lower anthocyanin contents in blood oranges at the ripening stage in local orchards, we compared the effects of postharvest storage at different temperatures on anthocyanin production in the pulps of fruit. Transcriptome sequencing and non-targeted metabolomics methods were used to analyze the dynamic changes in differentially expressed genes and differentially accumulated metabolites, respectively, during storage at 8 ℃ or room temperature (15 ℃). The results indicated that anthocyanin and citrate contents in fruit were higher at 8 ℃ than at other storage temperatures. The mRNA levels of TT8, a bHLH transcription factor, were higher in fruits stored at 8 ℃ than at room temperature throughout the entire storage period. Conversely, alternative splicing transcripts of TT8△, lacking a partial coding sequence, exhibited lower expression levels in fruit stored at 8 ℃. During postharvest storage, the genes involved in flavonoid biosynthesis and proton pumping were activated by TT8 and its partners. So that the increasing anthocyanin contents in juice sac tissues were attributed partially to TT8 expression changes caused by the alternative splicing during postharvest storage at a moderate temperature.</p>","PeriodicalId":20064,"journal":{"name":"Plant Molecular Biology","volume":"115 6","pages":"122"},"PeriodicalIF":3.8000,"publicationDate":"2025-10-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Integration of transcriptome and metabolome analysis reveals that alternative splicing of TT8 modulates anthocyanin biosynthesis in postharvest blood orange stored at moderate temperature.\",\"authors\":\"Wang Jianhui, Xu Rui, Guo Weiqing, Li Zhihong, Liu Dayu, Li Jingjing, Li Dagang, Chen Ying\",\"doi\":\"10.1007/s11103-025-01651-0\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>To address the problem of lower anthocyanin contents in blood oranges at the ripening stage in local orchards, we compared the effects of postharvest storage at different temperatures on anthocyanin production in the pulps of fruit. Transcriptome sequencing and non-targeted metabolomics methods were used to analyze the dynamic changes in differentially expressed genes and differentially accumulated metabolites, respectively, during storage at 8 ℃ or room temperature (15 ℃). The results indicated that anthocyanin and citrate contents in fruit were higher at 8 ℃ than at other storage temperatures. The mRNA levels of TT8, a bHLH transcription factor, were higher in fruits stored at 8 ℃ than at room temperature throughout the entire storage period. Conversely, alternative splicing transcripts of TT8△, lacking a partial coding sequence, exhibited lower expression levels in fruit stored at 8 ℃. During postharvest storage, the genes involved in flavonoid biosynthesis and proton pumping were activated by TT8 and its partners. So that the increasing anthocyanin contents in juice sac tissues were attributed partially to TT8 expression changes caused by the alternative splicing during postharvest storage at a moderate temperature.</p>\",\"PeriodicalId\":20064,\"journal\":{\"name\":\"Plant Molecular Biology\",\"volume\":\"115 6\",\"pages\":\"122\"},\"PeriodicalIF\":3.8000,\"publicationDate\":\"2025-10-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plant Molecular Biology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1007/s11103-025-01651-0\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Molecular Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s11103-025-01651-0","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Integration of transcriptome and metabolome analysis reveals that alternative splicing of TT8 modulates anthocyanin biosynthesis in postharvest blood orange stored at moderate temperature.
To address the problem of lower anthocyanin contents in blood oranges at the ripening stage in local orchards, we compared the effects of postharvest storage at different temperatures on anthocyanin production in the pulps of fruit. Transcriptome sequencing and non-targeted metabolomics methods were used to analyze the dynamic changes in differentially expressed genes and differentially accumulated metabolites, respectively, during storage at 8 ℃ or room temperature (15 ℃). The results indicated that anthocyanin and citrate contents in fruit were higher at 8 ℃ than at other storage temperatures. The mRNA levels of TT8, a bHLH transcription factor, were higher in fruits stored at 8 ℃ than at room temperature throughout the entire storage period. Conversely, alternative splicing transcripts of TT8△, lacking a partial coding sequence, exhibited lower expression levels in fruit stored at 8 ℃. During postharvest storage, the genes involved in flavonoid biosynthesis and proton pumping were activated by TT8 and its partners. So that the increasing anthocyanin contents in juice sac tissues were attributed partially to TT8 expression changes caused by the alternative splicing during postharvest storage at a moderate temperature.
期刊介绍:
Plant Molecular Biology is an international journal dedicated to rapid publication of original research articles in all areas of plant biology.The Editorial Board welcomes full-length manuscripts that address important biological problems of broad interest, including research in comparative genomics, functional genomics, proteomics, bioinformatics, computational biology, biochemical and regulatory networks, and biotechnology. Because space in the journal is limited, however, preference is given to publication of results that provide significant new insights into biological problems and that advance the understanding of structure, function, mechanisms, or regulation. Authors must ensure that results are of high quality and that manuscripts are written for a broad plant science audience.