Number of the records: 1  

RALF1 peptide triggers biphasic root growth inhibition upstream of auxin biosynthesis

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    SYSNO ASEP0564399
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleRALF1 peptide triggers biphasic root growth inhibition upstream of auxin biosynthesis
    Author(s) Li, L. (AT)
    Chen, H. (GB)
    Alotaibi, S. S. (SA)
    Pěnčík, Aleš (UEB-Q) ORCID, RID, SAI
    Adamowski, M. (AT)
    Novák, Ondřej (UEB-Q) RID, ORCID, SAI
    Friml, J. (AT)
    Number of authors7
    Article numbere2121058119
    Source TitleProceedings of the National Academy of Sciences of the United States of America. - : National Academy of Sciences - ISSN 0027-8424
    Roč. 119, č. 31 (2022)
    Number of pages10 s.
    Languageeng - English
    CountryUS - United States
    Keywordsauxin ; biphasic regulation ; cross-talk ; ralf1 ; root growth inhibition
    OECD categoryBiochemistry and molecular biology
    R&D ProjectsEF16_019/0000827 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    Method of publishingOpen access
    Institutional supportUEB-Q - RVO:61389030
    UT WOS000881496900002
    EID SCOPUS85135292745
    DOI10.1073/pnas.2121058119
    AnnotationPlant cell growth responds rapidly to various stimuli, adapting architecture to environmental changes. Two major endogenous signals regulating growth are the phytohormone auxin and the secreted peptides rapid alkalinization factors (RALFs). Both trigger very rapid cellular responses and also exert long-term effects [Du et al., Annu. Rev. Plant Biol. 71, 379–402 (2020), Blackburn et al., Plant Physiol. 182, 1657–1666 (2020)]. However, the way, in which these distinct signaling pathways converge to regulate growth, remains unknown. Here, using vertical confocal microscopy combined with a microfluidic chip, we addressed the mechanism of RALF action on growth. We observed correlation between RALF1-induced rapid Arabidopsis thaliana root growth inhibition and apoplast alkalinization during the initial phase of the response, and revealed that RALF1 reversibly inhibits primary root growth through apoplast alkalinization faster than within 1 min. This rapid apoplast alkalinization was the result of RALF1-induced net H+ influx and was mediated by the receptor FERONIA (FER). Furthermore, we investigated the cross-talk between RALF1 and the auxin signaling pathways during root growth regulation. The results showed that RALF-FER signaling triggered auxin signaling with a delay of approximately 1 h by up-regulating auxin biosynthesis, thus contributing to sustained RALF1-induced growth inhibition. This biphasic RALF1 action on growth allows plants to respond rapidly to environmental stimuli and also reprogram growth and development in the long term.
    WorkplaceInstitute of Experimental Botany
    ContactDavid Klier, knihovna@ueb.cas.cz, Tel.: 220 390 469
    Year of Publishing2023
    Electronic addresshttps://doi.org/10.1073/pnas.2121058119
Number of the records: 1  

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