IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v16y2025i1d10.1038_s41467-025-59329-6.html
   My bibliography  Save this article

Unveiling the regulatory role of GRP7 in ABA signal-mediated mRNA translation efficiency regulation

Author

Listed:
  • Jing Zhang

    (Chinese Academy of Sciences
    University of Chinese Academy of Sciences)

  • Wenna Shao

    (Shanghai Jiao Tong University)

  • Yongxin Xu

    (Chinese Academy of Sciences
    University of Chinese Academy of Sciences)

  • Fa’an Tian

    (University of Chinese Academy of Sciences
    Chinese Academy of Sciences)

  • Jinchao Chen

    (Chinese Academy of Sciences
    University of Chinese Academy of Sciences)

  • Dongzhi Wang

    (Chinese Academy of Sciences)

  • Xuelei Lin

    (Chinese Academy of Sciences)

  • Chongsheng He

    (Hunan University)

  • Xiaofei Yang

    (Norwich Research Park
    Chinese Academy of Sciences)

  • Dorothee Staiger

    (Bielefeld University)

  • Yiliang Ding

    (Norwich Research Park)

  • Xiang Yu

    (Shanghai Jiao Tong University)

  • Jun Xiao

    (Chinese Academy of Sciences
    University of Chinese Academy of Sciences
    CAS)

Abstract

Abscisic acid (ABA) is a crucial phytohormone involved in plant growth and stress responses. While the transcriptional regulation triggered by ABA is well-documented, its effects on translational regulation have been less studied. Through Ribo-seq and RNA-seq analyses, we find that ABA treatment not only influences gene expression at the mRNA level but also significantly impacts mRNA translation efficiency (TE) in Arabidopsis thaliana. ABA inhibits global mRNA translation via its core signaling pathway, which includes ABA receptors, protein phosphatase 2Cs (PP2Cs), and SNF1-related protein kinase 2 s (SnRK2s). Upon ABA treatment, Glycine-rich RNA-binding proteins 7 and 8 (GRP7&8) protein levels decrease due to both reduced mRNA level and decreased TE, which diminishes their association with polysomes and leads to a global decline in mRNA TE. The absence of GRP7&8 results in a global impairment of ABA-regulated translational changes, linking ABA signaling to GRP7-dependent modulation of mRNA translation. The regulation of GRP7 on TE relies significantly on its direct binding to target mRNAs. Moreover, mRNA translation efficiency under drought stress is partially dependent on the ABA-GRP7&8 pathways. Collectively, our study reveals GRP7’s role downstream of SnRK2s in mediating translation regulation in ABA signaling, offering a model for ABA-triggered multi-route regulation of environmental adaptation.

Suggested Citation

  • Jing Zhang & Wenna Shao & Yongxin Xu & Fa’an Tian & Jinchao Chen & Dongzhi Wang & Xuelei Lin & Chongsheng He & Xiaofei Yang & Dorothee Staiger & Yiliang Ding & Xiang Yu & Jun Xiao, 2025. "Unveiling the regulatory role of GRP7 in ABA signal-mediated mRNA translation efficiency regulation," Nature Communications, Nature, vol. 16(1), pages 1-18, December.
  • Handle: RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-59329-6
    DOI: 10.1038/s41467-025-59329-6
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-025-59329-6
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-025-59329-6?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
    ---><---

    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_s41467-025-59329-6. 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.

    We have no bibliographic references for this item. You can help adding them by using 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.