Xue Bai, ShengYang Wu, Ai‐Ning Bai, Yu‐Meng Zhang, Yan Zhang, Xue‐Feng Yao, Tao Yang, Meng‐Meng Chen, Jin‐Lei Liu, Lei Li, Yao Zhou, Chun‐Ming Liu
{"title":"OsSPL9 promotes Cu uptake and translocation in rice grown in high‐Fe red soil","authors":"Xue Bai, ShengYang Wu, Ai‐Ning Bai, Yu‐Meng Zhang, Yan Zhang, Xue‐Feng Yao, Tao Yang, Meng‐Meng Chen, Jin‐Lei Liu, Lei Li, Yao Zhou, Chun‐Ming Liu","doi":"10.1111/nph.70074","DOIUrl":null,"url":null,"abstract":"Summary<jats:list list-type=\"bullet\"> <jats:list-item>Most rice varieties are able to grow in red high‐Fe soil, but the underlying mechanism remains elusive.</jats:list-item> <jats:list-item>Through forward genetic screening, we identified a <jats:italic>red soil‐sensitive</jats:italic>‐<jats:italic>1</jats:italic> (<jats:italic>rss1</jats:italic>) mutant that exhibited severely retarded growth when grown in red soil but showed no evident phenotype in cinnamon soil.</jats:list-item> <jats:list-item>Under the red soil/high‐Fe conditions, <jats:italic>rss1</jats:italic> exhibited increased Fe but decreased copper (Cu) concentrations in both roots and shoots, and the <jats:italic>rss1</jats:italic> phenotype was partially rescued by Cu supplement. <jats:italic>RSS1</jats:italic> encodes an <jats:italic>OsSPL9</jats:italic> transcription factor that is expressed in pericycle cells and parenchyma cells surrounding xylem in roots. Under high‐Fe conditions, OsSPL9 activated expression of Cu transporters, including <jats:italic>OsYSL16</jats:italic>, <jats:italic>OsCOPT1</jats:italic>, and <jats:italic>OsCOPT5</jats:italic> by binding to their promoters, and <jats:italic>OsYSL16</jats:italic> overexpression partially rescued <jats:italic>rss1</jats:italic> defects.</jats:list-item> <jats:list-item>We thus propose that OsSPL9 overcomes high‐Fe imposed Cu deficiency by activating the expressions of Cu transporter genes, allowing rice to adapt to red soil.</jats:list-item> </jats:list>","PeriodicalId":214,"journal":{"name":"New Phytologist","volume":"28 1","pages":""},"PeriodicalIF":8.3000,"publicationDate":"2025-03-24","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.70074","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
SummaryMost rice varieties are able to grow in red high‐Fe soil, but the underlying mechanism remains elusive.Through forward genetic screening, we identified a red soil‐sensitive‐1 (rss1) mutant that exhibited severely retarded growth when grown in red soil but showed no evident phenotype in cinnamon soil.Under the red soil/high‐Fe conditions, rss1 exhibited increased Fe but decreased copper (Cu) concentrations in both roots and shoots, and the rss1 phenotype was partially rescued by Cu supplement. RSS1 encodes an OsSPL9 transcription factor that is expressed in pericycle cells and parenchyma cells surrounding xylem in roots. Under high‐Fe conditions, OsSPL9 activated expression of Cu transporters, including OsYSL16, OsCOPT1, and OsCOPT5 by binding to their promoters, and OsYSL16 overexpression partially rescued rss1 defects.We thus propose that OsSPL9 overcomes high‐Fe imposed Cu deficiency by activating the expressions of Cu transporter genes, allowing rice to adapt to red soil.
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.