2009
DOI: 10.1007/s11104-009-0080-4
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Cell death in wheat roots induced by the powdery mildew fungus Blumeria graminis f. sp. tritici

Abstract: Inoculation of wheat (Triticum aestivum L. cv. Huamai 8) leaves with wheat powderly mildew fungus (Blumeria graminis f. sp. tritici) induced cell death in wheat adventitious roots, where no fungal structures were observed. The cytological and molecular characterization of this cell death was shown as following: cell nuclei were TUNEL positive labeled; genomic DNA was fragmented and showed DNA laddering; chromatin condensed and formed peripheral conglomeration in nuclei; and perinuclear spaces partly dilated. T… Show more

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Cited by 15 publications
(8 citation statements)
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“…DNA fragmentation, an indicator of PCD as assessed by TUNEL-positive nuclei, occurred in cortical cells of wheat and barley seminal roots and was used to phenotype RCS. (Henry and Deacon 1981;Liljeroth and Bryngelsson 2002;Deng et al 2010). In addition, the use of a single-cell pressure probe enabled the quantification of RCS along a root (Bingham 2007).…”
Section: Quantifying Rcsmentioning
confidence: 99%
“…DNA fragmentation, an indicator of PCD as assessed by TUNEL-positive nuclei, occurred in cortical cells of wheat and barley seminal roots and was used to phenotype RCS. (Henry and Deacon 1981;Liljeroth and Bryngelsson 2002;Deng et al 2010). In addition, the use of a single-cell pressure probe enabled the quantification of RCS along a root (Bingham 2007).…”
Section: Quantifying Rcsmentioning
confidence: 99%
“…The samples were first fixed in 3 % paraformaldehyde and embedded in the Tissue-Tek OCT 4583 compound (Sakura Finetek,USA), and then, sections (20 μm) were made on a Leica CM l850 (Germany). Detection methods followed Deng et al (2010): Frozen sections were stained with 5 μM H 2 DCF-DA for 1 h and then washed by 0.1 M phosphate buffer. Frozen sections were photographed under a fluorescence microscope (Nikon Eclipse 80i; Japan).…”
Section: Ros Fluorescence Detectionmentioning
confidence: 99%
“…The fluorescence intensity at 530 nm normalised to the protein content was used to express ROS presence. Fluorescence of DCF derived from ROS oxidation was also observed under a fluorescence binocular (Olympus SZX12; excitation 450-490 nm, emission C520 nm) (Deng et al 2010). …”
Section: Measurement Of Ros Levelmentioning
confidence: 99%