{"title":"Reactive oxygen species act as signaling molecules to control root hair initiation and tip growth.","authors":"Megan E Gerber,Maleana G White,Gloria K Muday","doi":"10.1111/nph.70306","DOIUrl":null,"url":null,"abstract":"Root hairs (RHs) increase the surface area of roots, facilitating nutrient and water uptake and plant anchorage. RHs form from root epidermal cells and elongate by polar tip growth. Reactive oxygen species (ROS) have recently been implicated as important signals that drive RH formation and elongation using both genetic and imaging approaches. Localized changes in ROS levels in the RH tip are facilitated by hormone-mediated changes in the synthesis and activity of respiratory burst oxidase homologs and class III peroxidases. These findings broaden our understanding of the mechanisms controlling polar tip growth in plants that drive RH formation, which can inform the breeding and engineering of plants that thrive under drought and nutrient stress.","PeriodicalId":214,"journal":{"name":"New Phytologist","volume":"55 1","pages":""},"PeriodicalIF":8.1000,"publicationDate":"2025-06-25","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.70306","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
Root hairs (RHs) increase the surface area of roots, facilitating nutrient and water uptake and plant anchorage. RHs form from root epidermal cells and elongate by polar tip growth. Reactive oxygen species (ROS) have recently been implicated as important signals that drive RH formation and elongation using both genetic and imaging approaches. Localized changes in ROS levels in the RH tip are facilitated by hormone-mediated changes in the synthesis and activity of respiratory burst oxidase homologs and class III peroxidases. These findings broaden our understanding of the mechanisms controlling polar tip growth in plants that drive RH formation, which can inform the breeding and engineering of plants that thrive under drought and nutrient stress.
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.