{"title":"ABA insensitive 5 mediates abscisic acid regulation of plant photosynthesis by coordinating carbon and nitrogen assimilation","authors":"Qiaoying Long, Yuxuan Huang, Heping Xie, Haohui He, Wenjing Miao, Wenle Xie, Hongjie Lin, Haijian Huang, Zhisheng Zhang, Xinxiang Peng, Guohui Zhu","doi":"10.1111/nph.70409","DOIUrl":null,"url":null,"abstract":"Summary<jats:list list-type=\"bullet\"> <jats:list-item>Photosynthesis is inextricably linked to plant biomass and productivity. Enhancing the capacity for photosynthetic carbon assimilation stands as a pivotal strategy to boost plant photosynthetic efficiency; however, progress remains limited.</jats:list-item> <jats:list-item>We identified the <jats:italic>rog1</jats:italic> (<jats:italic>repressors of glu1‐1 1</jats:italic>) mutant, which was screened as a genetic suppressor of <jats:italic>glu1‐1</jats:italic>, an aberrant variant of <jats:italic>Arabidopsis</jats:italic> ferredoxin‐dependent glutamate synthase (Fd‐GOGAT) impaired in ammonium assimilation and photosynthesis. The <jats:italic>ROG1</jats:italic> gene encodes the abscisic acid (ABA) biosynthesis enzyme ABA2.</jats:list-item> <jats:list-item>Exogenous ABA exerts inhibitory effects on carbon and nitrogen assimilation, thus diminishing photosynthetic rates, and these inhibitions are contingent upon ABA insensitive 5 (ABI5), a key component of the ABA signaling pathway. Further investigation revealed that ABI5 acts as a transcriptional repressor, directly interacting with the promoters of carbon assimilation genes <jats:italic>RCA</jats:italic>, <jats:italic>RBCS2B</jats:italic>, and <jats:italic>RBCS3B</jats:italic>, as well as the nitrogen assimilation gene <jats:italic>GLU1</jats:italic>, thereby impeding their transcriptional activity. Reducing <jats:italic>ABI5</jats:italic> expression led to increased photosynthetic efficiency, growth, and productivity in both <jats:italic>Arabidopsis</jats:italic> and rice.</jats:list-item> <jats:list-item>This study highlights the critical role of ABI5 in plant photosynthesis by coordinating carbon and nitrogen assimilation, presenting a promising approach to enhance photosynthetic efficiency and agricultural productivity.</jats:list-item> </jats:list>","PeriodicalId":214,"journal":{"name":"New Phytologist","volume":"21 1","pages":""},"PeriodicalIF":8.1000,"publicationDate":"2025-07-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"New Phytologist","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/nph.70409","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
SummaryPhotosynthesis is inextricably linked to plant biomass and productivity. Enhancing the capacity for photosynthetic carbon assimilation stands as a pivotal strategy to boost plant photosynthetic efficiency; however, progress remains limited.We identified the rog1 (repressors of glu1‐1 1) mutant, which was screened as a genetic suppressor of glu1‐1, an aberrant variant of Arabidopsis ferredoxin‐dependent glutamate synthase (Fd‐GOGAT) impaired in ammonium assimilation and photosynthesis. The ROG1 gene encodes the abscisic acid (ABA) biosynthesis enzyme ABA2.Exogenous ABA exerts inhibitory effects on carbon and nitrogen assimilation, thus diminishing photosynthetic rates, and these inhibitions are contingent upon ABA insensitive 5 (ABI5), a key component of the ABA signaling pathway. Further investigation revealed that ABI5 acts as a transcriptional repressor, directly interacting with the promoters of carbon assimilation genes RCA, RBCS2B, and RBCS3B, as well as the nitrogen assimilation gene GLU1, thereby impeding their transcriptional activity. Reducing ABI5 expression led to increased photosynthetic efficiency, growth, and productivity in both Arabidopsis and rice.This study highlights the critical role of ABI5 in plant photosynthesis by coordinating carbon and nitrogen assimilation, presenting a promising approach to enhance photosynthetic efficiency and agricultural productivity.
期刊介绍:
New Phytologist is an international electronic journal published 24 times a year. It is owned by the New Phytologist Foundation, a non-profit-making charitable organization dedicated to promoting plant science. The journal publishes excellent, novel, rigorous, and timely research and scholarship in plant science and its applications. The articles cover topics in five sections: Physiology & Development, Environment, Interaction, Evolution, and Transformative Plant Biotechnology. These sections encompass intracellular processes, global environmental change, and encourage cross-disciplinary approaches. The journal recognizes the use of techniques from molecular and cell biology, functional genomics, modeling, and system-based approaches in plant science. Abstracting and Indexing Information for New Phytologist includes Academic Search, AgBiotech News & Information, Agroforestry Abstracts, Biochemistry & Biophysics Citation Index, Botanical Pesticides, CAB Abstracts®, Environment Index, Global Health, and Plant Breeding Abstracts, and others.