LpSAPK9 phosphorylates and activates LpABF2/LpABF3 to transactivate expression of chlorophyll catabolic genes and promote leaf senescence in perennial ryegrass
{"title":"LpSAPK9 phosphorylates and activates LpABF2/LpABF3 to transactivate expression of chlorophyll catabolic genes and promote leaf senescence in perennial ryegrass","authors":"Yuwei Yang, Jing Xing, Huanhuan Hao, Hao Guan, Huadong Yang, Tingchao Yin, Yingjun Chi, Bin Xu, Jing Zhang","doi":"10.1111/tpj.70477","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>Leaf senescence is an active and tightly controlled process that is particularly important for perennial plants to survive over hostile environmental conditions. The phytohormone ABA plays a vital regulatory role in leaf senescence, and the subclass III SnRK2 family genes, such as SnRK2.2/2.3/2.6, are known as key components in ABA signaling. Yet, the functional roles and molecular mechanisms of subclass I SnRK2s in ABA-mediated leaf senescence remain less well understood. In this study, we characterized one subclass I SnRK2 kinase, LpSAPK9, in perennial ryegrass (<i>Lolium perenne</i>). LpSAPK9 was localized in both the chloroplast and the nucleus, and its gene expression was positively correlated with the process of leaf senescence. Overexpressing <i>LpSAPK9</i> accelerated developmental and drought/osmotic-induced leaf senescence. The interactive proteins of LpSAPK9, including LpABF2 and LpABF3, were identified using yeast two-hybrid (Y2H) library screening and confirmed by firefly luciferase complementation assay (LCA), bimolecular fluorescence complementation (BiFC), and co-immunoprecipitation (Co-IP) assays. Combining Y1H, <i>in planta</i> transactivation assay, and CUT&Tag-qPCR, we identified that LpABF2 and LpABF3 directly bound promoters of four chlorophyll catabolic genes (<i>LpSGR</i>, <i>LpNYC1</i>, <i>LpNOL</i>, and <i>LpPPH</i>) to activate their transcription. By phosphorylating the S89 and T130 amino acid residues in LpABF2 and the S122 in LpABF3, LpSAPK9 enhances the transcription activities of LpABF2/3 to promote chlorophyll degradation and leaf senescence. Interestingly, <i>LpSAPK9</i> overexpression not only accelerated these senescence processes but also reduced leaf ABA content and down-regulated ABA biosynthetic genes. Collectively, our results reveal that the LpSAPK9-LpABF2/LpABF3 module coordinately regulates the expression of chlorophyll catabolic genes to control leaf senescence in perennial ryegrass.</p>\n </div>","PeriodicalId":233,"journal":{"name":"The Plant Journal","volume":"123 6","pages":""},"PeriodicalIF":5.7000,"publicationDate":"2025-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Plant Journal","FirstCategoryId":"2","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/tpj.70477","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
Leaf senescence is an active and tightly controlled process that is particularly important for perennial plants to survive over hostile environmental conditions. The phytohormone ABA plays a vital regulatory role in leaf senescence, and the subclass III SnRK2 family genes, such as SnRK2.2/2.3/2.6, are known as key components in ABA signaling. Yet, the functional roles and molecular mechanisms of subclass I SnRK2s in ABA-mediated leaf senescence remain less well understood. In this study, we characterized one subclass I SnRK2 kinase, LpSAPK9, in perennial ryegrass (Lolium perenne). LpSAPK9 was localized in both the chloroplast and the nucleus, and its gene expression was positively correlated with the process of leaf senescence. Overexpressing LpSAPK9 accelerated developmental and drought/osmotic-induced leaf senescence. The interactive proteins of LpSAPK9, including LpABF2 and LpABF3, were identified using yeast two-hybrid (Y2H) library screening and confirmed by firefly luciferase complementation assay (LCA), bimolecular fluorescence complementation (BiFC), and co-immunoprecipitation (Co-IP) assays. Combining Y1H, in planta transactivation assay, and CUT&Tag-qPCR, we identified that LpABF2 and LpABF3 directly bound promoters of four chlorophyll catabolic genes (LpSGR, LpNYC1, LpNOL, and LpPPH) to activate their transcription. By phosphorylating the S89 and T130 amino acid residues in LpABF2 and the S122 in LpABF3, LpSAPK9 enhances the transcription activities of LpABF2/3 to promote chlorophyll degradation and leaf senescence. Interestingly, LpSAPK9 overexpression not only accelerated these senescence processes but also reduced leaf ABA content and down-regulated ABA biosynthetic genes. Collectively, our results reveal that the LpSAPK9-LpABF2/LpABF3 module coordinately regulates the expression of chlorophyll catabolic genes to control leaf senescence in perennial ryegrass.
期刊介绍:
Publishing the best original research papers in all key areas of modern plant biology from the world"s leading laboratories, The Plant Journal provides a dynamic forum for this ever growing international research community.
Plant science research is now at the forefront of research in the biological sciences, with breakthroughs in our understanding of fundamental processes in plants matching those in other organisms. The impact of molecular genetics and the availability of model and crop species can be seen in all aspects of plant biology. For publication in The Plant Journal the research must provide a highly significant new contribution to our understanding of plants and be of general interest to the plant science community.