IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v16y2025i1d10.1038_s41467-024-55480-8.html
   My bibliography  Save this article

PIN2-mediated self-organizing transient auxin flow contributes to auxin maxima at the tip of Arabidopsis cotyledons

Author

Listed:
  • Patricio Pérez-Henríquez

    (University of California
    Fujian Agriculture and Forestry University
    University of California)

  • Shingo Nagawa

    (Fujian Agriculture and Forestry University)

  • Zhongchi Liu

    (Shenzhen University of Advanced Technology
    Shenzhen)

  • Xue Pan

    (University of California
    University of Toronto-Scarborough)

  • Marta Michniewicz

    (Washington University
    700 W Chesterfield Pkwy W)

  • Wenxin Tang

    (Fujian Agriculture and Forestry University)

  • Carolyn Rasmussen

    (University of California)

  • Xinping Cui

    (University of California)

  • Jaimie Norman

    (University of California
    University of California)

  • Lucia Strader

    (Washington University
    Duke University)

  • Zhenbiao Yang

    (University of California
    Fujian Agriculture and Forestry University
    Shenzhen University of Advanced Technology
    Shenzhen)

Abstract

Directional auxin transport and formation of auxin maxima are critical for embryogenesis, organogenesis, pattern formation, and growth coordination in plants, but the mechanisms underpinning the initiation and establishment of these auxin dynamics are not fully understood. Here we show that a self-initiating and -terminating transient auxin flow along the marginal cells (MCs) contributes to the formation of an auxin maximum at the tip of Arabidopsis cotyledon that globally coordinates the interdigitation of puzzle-shaped pavement cells in the cotyledon epidermis. Prior to the interdigitation, indole butyric acid (IBA) is converted to indole acetic acid (IAA) to induce PIN2 accumulation and polarization in the marginal cells, leading to auxin flow toward and accumulation at the cotyledon tip. Once IAA levels at the cotyledon tip reaches a maximum, it activates pavement cell interdigitation as well as the accumulation of the IBA transporter TOB1 in MCs, which sequesters IBA to the vacuole and reduces IBA availability and IAA levels. The reduction of IAA levels results in PIN2 down-regulation and cessation of the auxin flow. Hence, our results elucidate a self-activating and self-terminating transient polar auxin transport system in cotyledons, contributing to the formation of localized auxin maxima that spatiotemporally coordinate pavement cell interdigitation.

Suggested Citation

  • Patricio Pérez-Henríquez & Shingo Nagawa & Zhongchi Liu & Xue Pan & Marta Michniewicz & Wenxin Tang & Carolyn Rasmussen & Xinping Cui & Jaimie Norman & Lucia Strader & Zhenbiao Yang, 2025. "PIN2-mediated self-organizing transient auxin flow contributes to auxin maxima at the tip of Arabidopsis cotyledons," Nature Communications, Nature, vol. 16(1), pages 1-13, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-024-55480-8
    DOI: 10.1038/s41467-024-55480-8
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-024-55480-8
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-024-55480-8?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    References listed on IDEAS

    as
    1. Verônica A. Grieneisen & Jian Xu & Athanasius F. M. Marée & Paulien Hogeweg & Ben Scheres, 2007. "Auxin transport is sufficient to generate a maximum and gradient guiding root growth," Nature, Nature, vol. 449(7165), pages 1008-1013, October.
    2. Xue Pan & Linjing Fang & Jianfeng Liu & Betul Senay-Aras & Wenwei Lin & Shuan Zheng & Tong Zhang & Jingzhe Guo & Uri Manor & Jaimie Norman & Weitao Chen & Zhenbiao Yang, 2020. "Auxin-induced signaling protein nanoclustering contributes to cell polarity formation," Nature Communications, Nature, vol. 11(1), pages 1-14, December.
    3. Ross Sager & Xu Wang & Kristine Hill & Byung-Chun Yoo & Jeffery Caplan & Alex Nedo & Thu Tran & Malcolm J. Bennett & Jung-Youn Lee, 2020. "Auxin-dependent control of a plasmodesmal regulator creates a negative feedback loop modulating lateral root emergence," Nature Communications, Nature, vol. 11(1), pages 1-10, December.
    4. Jozef Mravec & Petr Skůpa & Aurélien Bailly & Klára Hoyerová & Pavel Křeček & Agnieszka Bielach & Jan Petrášek & Jing Zhang & Vassilena Gaykova & York-Dieter Stierhof & Petre I. Dobrev & Kateřina Schw, 2009. "Subcellular homeostasis of phytohormone auxin is mediated by the ER-localized PIN5 transporter," Nature, Nature, vol. 459(7250), pages 1136-1140, June.
    5. Alicia Lardennois & Gabriella Pásti & Teresa Ferraro & Flora Llense & Pierre Mahou & Julien Pontabry & David Rodriguez & Samantha Kim & Shoichiro Ono & Emmanuel Beaurepaire & Christelle Gally & Michel, 2019. "An actin-based viscoplastic lock ensures progressive body-axis elongation," Nature, Nature, vol. 573(7773), pages 266-270, September.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Matthieu Pierre Platre & Santosh B. Satbhai & Lukas Brent & Matias F. Gleason & Min Cao & Magali Grison & Marie Glavier & Ling Zhang & Christophe Gaillochet & Christian Goeschl & Marco Giovannetti & B, 2022. "The receptor kinase SRF3 coordinates iron-level and flagellin dependent defense and growth responses in plants," Nature Communications, Nature, vol. 13(1), pages 1-18, December.
    2. Julien Moukhtar & Alain Trubuil & Katia Belcram & David Legland & Zhor Khadir & Aurélie Urbain & Jean-Christophe Palauqui & Philippe Andrey, 2019. "Cell geometry determines symmetric and asymmetric division plane selection in Arabidopsis early embryos," PLOS Computational Biology, Public Library of Science, vol. 15(2), pages 1-27, February.
    3. Szymon Stoma & Mikael Lucas & Jérôme Chopard & Marianne Schaedel & Jan Traas & Christophe Godin, 2008. "Flux-Based Transport Enhancement as a Plausible Unifying Mechanism for Auxin Transport in Meristem Development," PLOS Computational Biology, Public Library of Science, vol. 4(10), pages 1-15, October.
    4. Huaiguo Shang & Na Zhang & Zhouli Xie & Siyu Deng & Licong Yi & Xing Huang, 2021. "Genome-Wide Identification and Expression of the PIN Auxin Efflux Carrier Gene Family in Watermelon ( Citrullus lanatus )," Agriculture, MDPI, vol. 11(5), pages 1-11, May.
    5. Jian Huang & Lei Zhao & Shikha Malik & Benjamin R. Gentile & Va Xiong & Tzahi Arazi & Heather A. Owen & Jiří Friml & Dazhong Zhao, 2022. "Specification of female germline by microRNA orchestrated auxin signaling in Arabidopsis," Nature Communications, Nature, vol. 13(1), pages 1-14, December.
    6. Christian Luschnig & Jiří Friml, 2024. "Over 25 years of decrypting PIN-mediated plant development," Nature Communications, Nature, vol. 15(1), pages 1-12, December.
    7. Tao Zhou & Jiajia Chen & Yanhui Huang & Zhengyu Jin & Jianrong Li & Yan Li & Xiaofang Zeng, 2022. "Genome-Wide Identification and Expression Analysis of the PIN Auxin Transporter Gene Family in Zanthoxylum armatum DC," Agriculture, MDPI, vol. 12(9), pages 1-16, August.
    8. Dirk De Vos & Kris Vissenberg & Jan Broeckhove & Gerrit T S Beemster, 2014. "Putting Theory to the Test: Which Regulatory Mechanisms Can Drive Realistic Growth of a Root?," PLOS Computational Biology, Public Library of Science, vol. 10(10), pages 1-19, October.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-024-55480-8. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.