2010
DOI: 10.1016/j.ijpara.2010.03.010
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Short interfering RNA-mediated knockdown of drosha and pasha in undifferentiated Meloidogyne incognita eggs leads to irregular growth and embryonic lethality

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Cited by 32 publications
(36 citation statements)
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“…Surprisingly, 7 siRNAs (Minc03313, Minc03866, Minc05001, Minc10706, Minc14652, Minc17713, Minc07817) induced significant and reproducible increase in transcript abundance when qPCR was performed 24 h after soaking. A similar ‘bounce’ effect, that could be due to a response of the nematode RNAi machinery to increased siRNA quantities within the cells, had already been reported in PPN after gene silencing [21], [22], [23]. To test this ‘bounce’ effect, we performed qPCR analysis 16 h after soaking on Minc07817, Minc03866 and Minc05001.…”
Section: Resultsmentioning
confidence: 57%
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“…Surprisingly, 7 siRNAs (Minc03313, Minc03866, Minc05001, Minc10706, Minc14652, Minc17713, Minc07817) induced significant and reproducible increase in transcript abundance when qPCR was performed 24 h after soaking. A similar ‘bounce’ effect, that could be due to a response of the nematode RNAi machinery to increased siRNA quantities within the cells, had already been reported in PPN after gene silencing [21], [22], [23]. To test this ‘bounce’ effect, we performed qPCR analysis 16 h after soaking on Minc07817, Minc03866 and Minc05001.…”
Section: Resultsmentioning
confidence: 57%
“…It is possible that some of the six other genes that showed an increase of transcripts level at 24 h may also present an initial decrease at an earlier time point. Such bounce phenomenon has already been described in plant-parasitic nematodes [21], [22], [23]. Interestingly, the 13 siRNAs yielding effects on transcript level encompass 10 out of the 12 cases of reproducible significant reduction of infestation.…”
Section: Discussionmentioning
confidence: 62%
“…Short interference RNAs (siRNAs) have also been used to knockdown gene-specific FLP transcripts in G. pallida and M. incognita J2 (Dalzell et al 2010). The variability in the degradation enzymes between a free-living nematode, Panagrellus redivivus, and M. incognita have recently been investigated (Masler 2010).…”
Section: Neuropeptidesmentioning
confidence: 99%
“…Today, RNAi has become an established experimental technique in a number of parasitic nematodes to investigate the function of different genes. The successful application of RNAi as tool for functional genomics has also been demonstrated in plant parasitic nematodes including the sedentary endoparasitic nematodes Globodera pallida, Heterodera glycines and Meloidogyne incognita [10][11][12][13] as well as the migratory parasitic nematodes Radopholus similis [14] and Bursaphelenchus xylophilus [15][16][17][18].…”
Section: Introductionmentioning
confidence: 99%