Mengmeng Yin , Changhe Wei , Hanmei Du , Tengfei Lyu , Fan Luo , Wenfeng Zhang , Xiaoli Zhou , Chengbosen Wang , Lijuan Chen , Dongsun Lee
{"title":"综合分析R2R3-MYB转录因子,发现OsMYB1是水稻花青素合成的关键调控因子","authors":"Mengmeng Yin , Changhe Wei , Hanmei Du , Tengfei Lyu , Fan Luo , Wenfeng Zhang , Xiaoli Zhou , Chengbosen Wang , Lijuan Chen , Dongsun Lee","doi":"10.1016/j.plantsci.2025.112732","DOIUrl":null,"url":null,"abstract":"<div><div>R2R3-MYB transcription factors (TFs) are key regulators of plant development, stress responses, and secondary metabolism, with a central role in anthocyanin biosynthesis. However, a comprehensive understanding of the R2R3-MYB TFs involved in anthocyanin accumulation in rice (<em>Oryza sativa</em> L.) remains limited. In this study, we identified 105 R2R3-MYB TFs in the rice genome and performed extensive analyses of their phylogenetic relationships, conserved motifs, gene structures, and syntenic conservation across species. Integrating phylogenetic and expression profiling data, OsMYB1—belonging to subfamily 4 (S4) and homologous to AtMYB4—emerged as a key negative regulator of anthocyanin biosynthesis. Subcellular localization analysis confirmed that OsMYB1 is localized predominantly in the nucleus. Functional assays demonstrated that OsMYB1 binds to the promoters of <em>OsDFR</em> and <em>OsANS</em>, repressing their transcription. Moreover, OsMYB1 interacts with core components of the MYB-bHLH-WD40 (MBW) activation complex, specifically OsB2 and OsPAC1, to modulate anthocyanin biosynthesis via a negative feedback mechanism. CRISPR-Cas9-mediated knockout of OsMYB1 in purple rice varieties led to a marked increase in anthocyanin accumulation in pericarps and leaves, accompanied by upregulation of key biosynthetic genes such as <em>OsF3’H</em>, <em>OsDFR</em>, and <em>OsANS</em>. These findings establish OsMYB1 as a pivotal transcriptional repressor orchestrating anthocyanin biosynthesis in rice, providing valuable insights into the regulatory networks governing flavonoid pathways. This work offers promising genetic targets for biofortification and crop improvement strategies aimed at enhancing nutritional quality and stress resilience in cereal crops.</div></div>","PeriodicalId":20273,"journal":{"name":"Plant Science","volume":"360 ","pages":"Article 112732"},"PeriodicalIF":4.1000,"publicationDate":"2025-08-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Comprehensive analysis of R2R3-MYB transcription factors reveals OsMYB1 as a key regulator of anthocyanin biosynthesis in rice\",\"authors\":\"Mengmeng Yin , Changhe Wei , Hanmei Du , Tengfei Lyu , Fan Luo , Wenfeng Zhang , Xiaoli Zhou , Chengbosen Wang , Lijuan Chen , Dongsun Lee\",\"doi\":\"10.1016/j.plantsci.2025.112732\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>R2R3-MYB transcription factors (TFs) are key regulators of plant development, stress responses, and secondary metabolism, with a central role in anthocyanin biosynthesis. However, a comprehensive understanding of the R2R3-MYB TFs involved in anthocyanin accumulation in rice (<em>Oryza sativa</em> L.) remains limited. In this study, we identified 105 R2R3-MYB TFs in the rice genome and performed extensive analyses of their phylogenetic relationships, conserved motifs, gene structures, and syntenic conservation across species. Integrating phylogenetic and expression profiling data, OsMYB1—belonging to subfamily 4 (S4) and homologous to AtMYB4—emerged as a key negative regulator of anthocyanin biosynthesis. Subcellular localization analysis confirmed that OsMYB1 is localized predominantly in the nucleus. Functional assays demonstrated that OsMYB1 binds to the promoters of <em>OsDFR</em> and <em>OsANS</em>, repressing their transcription. Moreover, OsMYB1 interacts with core components of the MYB-bHLH-WD40 (MBW) activation complex, specifically OsB2 and OsPAC1, to modulate anthocyanin biosynthesis via a negative feedback mechanism. CRISPR-Cas9-mediated knockout of OsMYB1 in purple rice varieties led to a marked increase in anthocyanin accumulation in pericarps and leaves, accompanied by upregulation of key biosynthetic genes such as <em>OsF3’H</em>, <em>OsDFR</em>, and <em>OsANS</em>. These findings establish OsMYB1 as a pivotal transcriptional repressor orchestrating anthocyanin biosynthesis in rice, providing valuable insights into the regulatory networks governing flavonoid pathways. This work offers promising genetic targets for biofortification and crop improvement strategies aimed at enhancing nutritional quality and stress resilience in cereal crops.</div></div>\",\"PeriodicalId\":20273,\"journal\":{\"name\":\"Plant Science\",\"volume\":\"360 \",\"pages\":\"Article 112732\"},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2025-08-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plant Science\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0168945225003504\",\"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 Science","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0168945225003504","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}
Comprehensive analysis of R2R3-MYB transcription factors reveals OsMYB1 as a key regulator of anthocyanin biosynthesis in rice
R2R3-MYB transcription factors (TFs) are key regulators of plant development, stress responses, and secondary metabolism, with a central role in anthocyanin biosynthesis. However, a comprehensive understanding of the R2R3-MYB TFs involved in anthocyanin accumulation in rice (Oryza sativa L.) remains limited. In this study, we identified 105 R2R3-MYB TFs in the rice genome and performed extensive analyses of their phylogenetic relationships, conserved motifs, gene structures, and syntenic conservation across species. Integrating phylogenetic and expression profiling data, OsMYB1—belonging to subfamily 4 (S4) and homologous to AtMYB4—emerged as a key negative regulator of anthocyanin biosynthesis. Subcellular localization analysis confirmed that OsMYB1 is localized predominantly in the nucleus. Functional assays demonstrated that OsMYB1 binds to the promoters of OsDFR and OsANS, repressing their transcription. Moreover, OsMYB1 interacts with core components of the MYB-bHLH-WD40 (MBW) activation complex, specifically OsB2 and OsPAC1, to modulate anthocyanin biosynthesis via a negative feedback mechanism. CRISPR-Cas9-mediated knockout of OsMYB1 in purple rice varieties led to a marked increase in anthocyanin accumulation in pericarps and leaves, accompanied by upregulation of key biosynthetic genes such as OsF3’H, OsDFR, and OsANS. These findings establish OsMYB1 as a pivotal transcriptional repressor orchestrating anthocyanin biosynthesis in rice, providing valuable insights into the regulatory networks governing flavonoid pathways. This work offers promising genetic targets for biofortification and crop improvement strategies aimed at enhancing nutritional quality and stress resilience in cereal crops.
期刊介绍:
Plant Science will publish in the minimum of time, research manuscripts as well as commissioned reviews and commentaries recommended by its referees in all areas of experimental plant biology with emphasis in the broad areas of genomics, proteomics, biochemistry (including enzymology), physiology, cell biology, development, genetics, functional plant breeding, systems biology and the interaction of plants with the environment.
Manuscripts for full consideration should be written concisely and essentially as a final report. The main criterion for publication is that the manuscript must contain original and significant insights that lead to a better understanding of fundamental plant biology. Papers centering on plant cell culture should be of interest to a wide audience and methods employed result in a substantial improvement over existing established techniques and approaches. Methods papers are welcome only when the technique(s) described is novel or provides a major advancement of established protocols.