2014
DOI: 10.4161/psb.29376
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Gene silencing ofCCD7andCCD8inPhelipanche aegyptiacaby tobacco rattle virus system retarded the parasite development on the host

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Cited by 26 publications
(25 citation statements)
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“…9 Strigolactones, the major class of germination stimulants, 14 are derived from carotenoids through two subsequent enzymatic cleavage steps performed by the carotenoid cleaving dioxygenases CCD7 and CCD8. [29][30][31][32] To date, the impact of virus-infected host plant on parasitism by Phelipanche has not been reported, therefore our study focused on carotenoid content in CMV-infected tobacco roots and its effect on the development of the parasite.…”
Section: Resultsmentioning
confidence: 99%
“…9 Strigolactones, the major class of germination stimulants, 14 are derived from carotenoids through two subsequent enzymatic cleavage steps performed by the carotenoid cleaving dioxygenases CCD7 and CCD8. [29][30][31][32] To date, the impact of virus-infected host plant on parasitism by Phelipanche has not been reported, therefore our study focused on carotenoid content in CMV-infected tobacco roots and its effect on the development of the parasite.…”
Section: Resultsmentioning
confidence: 99%
“…2-5). The stunted growth of crop plants that were parasitized by broomrapes was reported for different host-parasite associations and under different growth conditions 10,[35][36][37][38] . Westwood 39 discussed the alteration in the physiology/metabolism of the host, and/or the reduction in the potential of the infested host root system to take up nutrients/water from the soil leading to a reduction in assimilate production.…”
Section: Discussionmentioning
confidence: 99%
“…Powerful CRISPR-Cas9 technique was successfully used for mutagenesis of the CCD8 (Carotenoid Cleavage Dioxygenase 8) gene, strigolactone-biosynthesis gene, in order to create Phelipanche aegyptica resistant tomato lines [99]. Another gene silencing technique, virus-induced gene silencing (VIGS) was used to induce trans-silencing of PaCCD7 and PaCCD8 genes in P. aegyptica for significant reduction in the number of parasite tubercles attached to Nicotiana benthamiana roots [100]. New gene editing techniques can be difficult to apply in sunflower breeding, mainly due to the difficulties that occur during plant regeneration and low numbers of obtained transgenic regenerants per assay.…”
Section: Future Prospects and New Approachesmentioning
confidence: 99%