2018
DOI: 10.1016/j.plaphy.2018.02.023
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A peptidogalactomannan isolated from Cladosporium herbarum induces defense-related genes in BY-2 tobacco cells

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Cited by 11 publications
(17 citation statements)
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“…The BY-2 protoplast is proved to be an effective system for agents screening and clarification of their mode of action. For example, BY-2 cells were treated with microbial-derived metabolite from Cladosporium herbarum , which results in significant up-regulation of host defense-related genes [66]. In this study, our results showed that NNM treatment effectively inhibited viral RNA accumulation of TMV and significantly regulated many lines of potential virus resistance genes in the tobacco BY-2 protoplasts.…”
Section: Discussionmentioning
confidence: 64%
“…The BY-2 protoplast is proved to be an effective system for agents screening and clarification of their mode of action. For example, BY-2 cells were treated with microbial-derived metabolite from Cladosporium herbarum , which results in significant up-regulation of host defense-related genes [66]. In this study, our results showed that NNM treatment effectively inhibited viral RNA accumulation of TMV and significantly regulated many lines of potential virus resistance genes in the tobacco BY-2 protoplasts.…”
Section: Discussionmentioning
confidence: 64%
“…Livak and Schmitgen [21]. Primers used for qPCR analysis were described by Mattos et al, 2018. Annealing temperature of all genes evaluated was 60˚C, except for PAL and PR5, whose annealing temperature was 62˚C.…”
Section: Plos Onementioning
confidence: 99%
“…PR-1 (pathogenesis related protein-1 with suggested antifungal action), PR-2 (β-1,3-glucanase), PR-3 (chitinase), PR-5 (osmotin/thaumatin-like), PAL (phenylalanine ammonia-lyase), LOX (lipoxygenase) and POX (Peroxidase) genes expression was evaluated. PP2A (phosphatase 2A) and Ntbuc (ubiquitin) were used to normalize cDNA expression levels [22].…”
Section: Plos Onementioning
confidence: 99%
“…cDNA amplification reactions were performed in a final volume of 25 μl, according to the manufacturer's guidelines. qPCR cycles were 10 minutes at 95°C for initial denaturation, followed by 40 cycles of denaturation at 95°C for 15 sec and annealing/extension at 60°C for 1 minute, except for the PAL and PR5 genes, for which the annealing temperature was adjusted to 62°C [23]. The results were analyzed by the 2 −△△ CT method according to [29].…”
Section: Analysis Of Defense Gene Expression By Qrt-pcrmentioning
confidence: 99%
“…β-D-Galactofuranosyl residues were present as (1→5)-interlinked side chains of C. herbarum pGM. The role of pGM cell wall glycoprotein in plant-fungus interactions was first studied by Mattos et al [23], who showed the induction of the expression of defense genes in tobacco BY2 cells and a hypersensitive response (HR) after treatment of tobacco leaves with C. herbarum pGM. This recognition and defense response activation would possibly contribute to the plant response to the pathogen attack, protecting itself against new infections and indicating that pGM is probably able to induce SAR.…”
Section: Introductionmentioning
confidence: 99%