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Exocyst subunit EXO70H4 has a specific role in callose synthase secretion and silica accumulation
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SYSNO ASEP 0488738 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Článek ve WOS Title Exocyst 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, ORCIDNumber of authors 7 Source Title Plant Physiology. - : Oxford University Press - ISSN 0032-0889
Roč. 176, č. 3 (2018), s. 2040-2051Number of pages 12 s. Language eng - English Country US - United States Keywords COMPLETE PENETRATION RESISTANCE ; SCANNING-ELECTRON-MICROSCOPE ; POWDERY MILDEW Subject RIV EB - Genetics ; Molecular Biology OECD category Cell biology Subject RIV - cooperation Institute of Scientific Instruments - Electronics ; Optoelectronics, Electrical Engineering Institutional support UEB-Q - RVO:61389030 ; UPT-D - RVO:68081731 UT WOS 000426848300018 EID SCOPUS 85044003089 DOI 10.1104/pp.17.01693 Annotation Biogenesis 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. Workplace Institute of Experimental Botany Contact David Klier, knihovna@ueb.cas.cz, Tel.: 220 390 469 Year of Publishing 2019
Number of the records: 1