2013
DOI: 10.1007/s11248-013-9739-y
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Plant-mediated RNAi of a gap gene-enhanced tobacco tolerance against the Myzus persicae

Abstract: Plant-mediated RNAi has been developed as a powerful weapon in the fight against agricultural insect pests. The gap gene hunchback (hb) is of crucial importance in insect axial patterning and knockdown of hb is deforming and lethal to the next generation. The peach potato aphid, Myzus persicae (Sulzer), has many host plants and can be found throughout the world. To investigate the effect of plant-mediated RNAi on control of this insect, the hb gene in M. persicae was cloned, plant RNAi vector was constructed, … Show more

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Cited by 96 publications
(77 citation statements)
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“…Recently, Mao and Zhang [75] targeted the gap gene hunchback in M. persicae, which had previously been shown to be an effective target in A. pisum when fed in artificial diet. Feeding of transgenic tobacco expressing dsRNA targeting hunchback of M. persicae, however, elicited different results.…”
Section: Nilaparvata Lugensmentioning
confidence: 99%
“…Recently, Mao and Zhang [75] targeted the gap gene hunchback in M. persicae, which had previously been shown to be an effective target in A. pisum when fed in artificial diet. Feeding of transgenic tobacco expressing dsRNA targeting hunchback of M. persicae, however, elicited different results.…”
Section: Nilaparvata Lugensmentioning
confidence: 99%
“…The gene of different insects has been knock downed via orally fed dsRNA including insects from Hymenoptera (Lynch and Desplan 2006), Coleoptera (Tomoyasu et al 2008), Diptera (Dzitoyeva et al 2001), Lepidoptera (Terenius et al 2011). However, results from reports of Mao et al (2011), Zhu et al (2012 and Mao and Zeng (2014) are more encouraging who knock downed Fig. 2 The efficacy of insecticidal genes in transgenic cotton evaluated by leaf biotoxicity and artificial insect infestation of plants.…”
Section: Insect-resistant Cottonmentioning
confidence: 99%
“…dsRNA or mature siRNA can activate RNA degradation in insect cells, and different methods to deliver these molecules into whole aphids have been employed [12,18]. Aphids can be fed on dsRNA or siRNA sources, such as (1) in vitro-synthesized dsRNA [19,20,21,22,23,24,25,26]; (2) siRNA synthesized chemically or obtained after enzymatic cleavage of the dsRNA [27,28]; or (3) plants stably or transiently expressing dsRNA [29,30,31,32,33,34]. An alternative method to deliver dsRNA or siRNA into aphids is by microinjection, although this technique is not well adapted to a large scale analysis of genes [19,22,27,28,30,35,36,37].…”
Section: Introductionmentioning
confidence: 99%