{"title":"Cell‐type‐specific PIN‐FORMED 3‐mediated polar auxin transport regulates cambial activity and tension wood formation in Populus tomentosa ","authors":"Dongmei Xiang, Lingmin Ran, Yuanjin Li, Liqing Zong, Baoxia Li, Qingqing Chu, Mi Zhang, Xiaokang Fu, Lianghanxiao Sun, Shutang Tan, Markus Geisler, Bangjun Wang, Xiaoyan Gu, Keming Luo, Changzheng Xu","doi":"10.1111/nph.71660","DOIUrl":null,"url":null,"abstract":"Summary <jats:list list-type=\"bullet\"> <jats:list-item> Auxin is a central regulator of tree secondary growth and forms maxima in the vascular cambium, yet how these maxima are established remains elusive. Here, we functionally characterized two redundant PIN‐FORMED 3 ( <jats:italic>PIN3</jats:italic> ) paralogs from <jats:italic>Populus tomentosa</jats:italic> to define their roles in secondary growth and gravity‐induced tension wood (TW) formation. </jats:list-item> <jats:list-item> We employed fluorescent reporter lines, clustered regularly interspaced short palindromic repeats‐generated knockout mutants, phloem‐specific RNA interference transgenic plants and isotopic auxin transport assays to dissect PIN3 functions during secondary growth of poplar stems. </jats:list-item> <jats:list-item> Loss of function of <jats:italic>PIN3</jats:italic> paralogs severely compromises cambial proliferation, secondary xylem differentiation and TW development. PIN3 proteins display cell‐type‐specific polar localization with basal polarity in phloem cells and outer lateral polarity in endodermal cells. Phloem‐expressed PIN3 facilitates basipetal auxin transport and is required for cambial auxin response. Upon gravistimulation, endodermal PIN3 repolarizes along the gravity vector, correlating with TW formation. </jats:list-item> <jats:list-item> Our findings identify a cell‐type‐specific, PIN3‐mediated auxin transport mechanism that contributes to auxin‐driven secondary growth of tree stems. </jats:list-item> </jats:list>","PeriodicalId":214,"journal":{"name":"New Phytologist","volume":"20 1","pages":""},"PeriodicalIF":8.7000,"publicationDate":"2026-10-18","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.71660","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
Summary Auxin is a central regulator of tree secondary growth and forms maxima in the vascular cambium, yet how these maxima are established remains elusive. Here, we functionally characterized two redundant PIN‐FORMED 3 ( PIN3 ) paralogs from Populus tomentosa to define their roles in secondary growth and gravity‐induced tension wood (TW) formation. We employed fluorescent reporter lines, clustered regularly interspaced short palindromic repeats‐generated knockout mutants, phloem‐specific RNA interference transgenic plants and isotopic auxin transport assays to dissect PIN3 functions during secondary growth of poplar stems. Loss of function of PIN3 paralogs severely compromises cambial proliferation, secondary xylem differentiation and TW development. PIN3 proteins display cell‐type‐specific polar localization with basal polarity in phloem cells and outer lateral polarity in endodermal cells. Phloem‐expressed PIN3 facilitates basipetal auxin transport and is required for cambial auxin response. Upon gravistimulation, endodermal PIN3 repolarizes along the gravity vector, correlating with TW formation. Our findings identify a cell‐type‐specific, PIN3‐mediated auxin transport mechanism that contributes to auxin‐driven secondary growth of tree stems.
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.