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Exocyst subunit EXO70H4 has a specific role in callose synthase secretion and silica accumulation

  1. 1.
    SYSNO ASEP0488738
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleExocyst subunit EXO70H4 has a specific role in callose synthase secretion and silica accumulation
    Author(s) Kulich, I. (CZ)
    Vojtíková, Z. (CZ)
    Sabol, P. (CZ)
    Ortmannová, Jitka (UEB-Q) ORCID
    Neděla, Vilém (UPT-D) RID, ORCID, SAI
    Tihlaříková, Eva (UPT-D) RID, ORCID, SAI
    Žárský, Viktor (UEB-Q) RID, ORCID
    Number of authors7
    Source TitlePlant Physiology. - : Oxford University Press - ISSN 0032-0889
    Roč. 176, č. 3 (2018), s. 2040-2051
    Number of pages12 s.
    Languageeng - English
    CountryUS - United States
    KeywordsCOMPLETE PENETRATION RESISTANCE ; SCANNING-ELECTRON-MICROSCOPE ; POWDERY MILDEW
    Subject RIVEB - Genetics ; Molecular Biology
    OECD categoryCell biology
    Subject RIV - cooperationInstitute of Scientific Instruments - Electronics ; Optoelectronics, Electrical Engineering
    Institutional supportUEB-Q - RVO:61389030 ; UPT-D - RVO:68081731
    UT WOS000426848300018
    EID SCOPUS85044003089
    DOI10.1104/pp.17.01693
    AnnotationBiogenesis of the plant secondary cell wall involves many important aspects, such as phenolic compound deposition and often silica encrustation. Previously, we demonstrated the importance of the exocyst subunit EXO70H4 for biogenesis of the trichome secondary cell wall, namely for deposition of the autofluorescent and callose-rich cell wall layer. Here, we reveal that EXO70H4-driven cell wall biogenesis is cons titutively active in the mature trichome, but also can be activated elsewhere upon pathogen attack, giving this study a broader significance with an overlap into phytopathology. To address the specificity of EXO70H4 among the EXO70 family, we complemented the exo70H4-1 mutant by 18 different Arabidopsis (Arabidopsis thaliana) EXO70 paralogs subcloned under the EXO70H4 promoter. Only EXO70H4 had the capacity to rescue the exo70H4-1 trichome phenotype. Callose deposition phenotype of exo70H4-1 mutant is caused by impaired secretion of PMR4, a callose synthase responsible for the synthesis of callose in the trichome. PMR4 colocalizes with EXO70H4 on plasma membrane microdomains that do not develop in the exo70H4-1 mutant. Using energy-dispersive x-ray microanalysis, we show that both EXO70H4- and PMR4-dependent callose deposition in the trichome are essential for cell wall silicification.
    WorkplaceInstitute of Experimental Botany
    ContactDavid Klier, knihovna@ueb.cas.cz, Tel.: 220 390 469
    Year of Publishing2019
Number of the records: 1  

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