IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v13y2022i1d10.1038_s41467-022-33384-9.html
   My bibliography  Save this article

A combination of plasma membrane sterol biosynthesis and autophagy is required for shade-induced hypocotyl elongation

Author

Listed:
  • Yetkin Çaka Ince

    (University of Lausanne)

  • Johanna Krahmer

    (University of Lausanne)

  • Anne-Sophie Fiorucci

    (University of Lausanne)

  • Martine Trevisan

    (University of Lausanne)

  • Vinicius Costa Galvão

    (University of Lausanne)

  • Leonore Wigger

    (University of Lausanne)

  • Sylvain Pradervand

    (University of Lausanne)

  • Laetitia Fouillen

    (Univ. Bordeaux, CNRS, Laboratoire de Biogenèse Membranaire, UMR 5200)

  • Pierre Delft

    (Univ. Bordeaux, CNRS, Laboratoire de Biogenèse Membranaire, UMR 5200)

  • Manon Genva

    (Univ. Bordeaux, CNRS, Laboratoire de Biogenèse Membranaire, UMR 5200
    University of Liège)

  • Sebastien Mongrand

    (Univ. Bordeaux, CNRS, Laboratoire de Biogenèse Membranaire, UMR 5200)

  • Hector Gallart-Ayala

    (University of Lausanne)

  • Julijana Ivanisevic

    (University of Lausanne)

  • Christian Fankhauser

    (University of Lausanne)

Abstract

Plant growth ultimately depends on fixed carbon, thus the available light for photosynthesis. Due to canopy light absorption properties, vegetative shade combines low blue (LB) light and a low red to far-red ratio (LRFR). In shade-avoiding plants, these two conditions independently trigger growth adaptations to enhance light access. However, how these conditions, differing in light quality and quantity, similarly promote hypocotyl growth remains unknown. Using RNA sequencing we show that these two features of shade trigger different transcriptional reprogramming. LB induces starvation responses, suggesting a switch to a catabolic state. Accordingly, LB promotes autophagy. In contrast, LRFR induced anabolism including expression of sterol biosynthesis genes in hypocotyls in a manner dependent on PHYTOCHROME-INTERACTING FACTORs (PIFs). Genetic analyses show that the combination of sterol biosynthesis and autophagy is essential for hypocotyl growth promotion in vegetative shade. We propose that vegetative shade enhances hypocotyl growth by combining autophagy-mediated recycling and promotion of specific lipid biosynthetic processes.

Suggested Citation

  • Yetkin Çaka Ince & Johanna Krahmer & Anne-Sophie Fiorucci & Martine Trevisan & Vinicius Costa Galvão & Leonore Wigger & Sylvain Pradervand & Laetitia Fouillen & Pierre Delft & Manon Genva & Sebastien , 2022. "A combination of plasma membrane sterol biosynthesis and autophagy is required for shade-induced hypocotyl elongation," Nature Communications, Nature, vol. 13(1), pages 1-17, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-33384-9
    DOI: 10.1038/s41467-022-33384-9
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-022-33384-9
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-022-33384-9?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. Géraldine Brunoud & Darren M. Wells & Marina Oliva & Antoine Larrieu & Vincent Mirabet & Amy H. Burrow & Tom Beeckman & Stefan Kepinski & Jan Traas & Malcolm J. Bennett & Teva Vernoux, 2012. "A novel sensor to map auxin response and distribution at high spatio-temporal resolution," Nature, Nature, vol. 482(7383), pages 103-106, February.
    2. Martina Legris & Yetkin Çaka Ince & Christian Fankhauser, 2019. "Molecular mechanisms underlying phytochrome-controlled morphogenesis in plants," Nature Communications, Nature, vol. 10(1), pages 1-15, December.
    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. Zenglin Li & David J. Sheerin & Edda Roepenack-Lahaye & Mark Stahl & Andreas Hiltbrunner, 2022. "The phytochrome interacting proteins ERF55 and ERF58 repress light-induced seed germination in Arabidopsis thaliana," Nature Communications, Nature, vol. 13(1), pages 1-18, December.
    2. Weixiao Yuan Wahlgren & Elin Claesson & Iida Tuure & Sergio Trillo-Muyo & Szabolcs Bódizs & Janne A. Ihalainen & Heikki Takala & Sebastian Westenhoff, 2022. "Structural mechanism of signal transduction in a phytochrome histidine kinase," Nature Communications, Nature, vol. 13(1), pages 1-8, December.
    3. Lulu Zheng & Yongfeng Hu & Tianzhao Yang & Zhen Wang & Daoyuan Wang & Letian Jia & Yuanming Xie & Long Luo & Weicong Qi & Yuanda Lv & Tom Beeckman & Wei Xuan & Yi Han, 2024. "A root cap-localized NAC transcription factor controls root halotropic response to salt stress in Arabidopsis," Nature Communications, Nature, vol. 15(1), pages 1-12, December.
    4. Urszula Piskurewicz & Maria Sentandreu & Mayumi Iwasaki & Gaëtan Glauser & Luis Lopez-Molina, 2023. "The Arabidopsis endosperm is a temperature-sensing tissue that implements seed thermoinhibition through phyB," Nature Communications, Nature, vol. 14(1), pages 1-14, December.
    5. Giacomo Salvadori & Veronica Macaluso & Giulia Pellicci & Lorenzo Cupellini & Giovanni Granucci & Benedetta Mennucci, 2022. "Protein control of photochemistry and transient intermediates in phytochromes," Nature Communications, Nature, vol. 13(1), pages 1-10, December.
    6. Ruth Jean Ae Kim & De Fan & Jiangman He & Keunhwa Kim & Juan Du & Meng Chen, 2024. "Photobody formation spatially segregates two opposing phytochrome B signaling actions of PIF5 degradation and stabilization," Nature Communications, Nature, vol. 15(1), pages 1-14, December.
    7. Chanhee Kim & Yongmin Kwon & Jaehoon Jeong & Minji Kang & Ga Seul Lee & Jeong Hee Moon & Hyo-Jun Lee & Youn-Il Park & Giltsu Choi, 2023. "Phytochrome B photobodies are comprised of phytochrome B and its primary and secondary interacting proteins," Nature Communications, Nature, vol. 14(1), pages 1-13, December.

    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:13:y:2022:i:1:d:10.1038_s41467-022-33384-9. 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.