2003
DOI: 10.1094/mpmi.2003.16.10.936
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Cucumber mosaic virus Infection Transiently Breaks dsRNA-Induced Transgenic Immunity to Potato virus Y in Tobacco

Abstract: Post-transcriptional gene silencing (PTGS), an intrinsic plant defense mechanism, can be efficiently triggered by double stranded (ds)RNA-producing transgenes and can provide high level virus resistance by specific targeting of cognate viral RNA. The discovery of virus-encoded suppressors of PTGS led to concerns about the stability of such resistance. Here, we show that Cucumber mosaic virus (CMV) is able to suppress dsRNA-induced PTGS and the associated Potato virus Y (PVY) immunity in tobacco. CMV suppressio… Show more

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Cited by 39 publications
(19 citation statements)
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“…Total RNA was isolated by using TRIzol reagent (Invitrogen, Carlsbad, CA) and used for highand low-molecular-weight RNA blot analysis, as well as RT-PCR analysis. Enrichment for low-molecular-weight RNA and Northern blot analysis was performed as described previously (47). Riboprobes were generated by using the Riboprobe Combination System, SP6/T7 kit (Promega, Madison, WI).…”
Section: Methodsmentioning
confidence: 99%
“…Total RNA was isolated by using TRIzol reagent (Invitrogen, Carlsbad, CA) and used for highand low-molecular-weight RNA blot analysis, as well as RT-PCR analysis. Enrichment for low-molecular-weight RNA and Northern blot analysis was performed as described previously (47). Riboprobes were generated by using the Riboprobe Combination System, SP6/T7 kit (Promega, Madison, WI).…”
Section: Methodsmentioning
confidence: 99%
“…The small RNA fraction (,400 nt) was recovered from total RNA using previously described methods (Mitter et al, 2003). Briefly, polyethylene glycol 8000 and NaCl were added to the total RNA solution and the volume adjusted to give final concentrations of 10 % (w/v) and 500 mM, respectively, followed by incubation on ice for 30 min.…”
Section: Methodsmentioning
confidence: 99%
“…RNA-gel (northern) blotting was carried out as described by Mitter et al (2003), except that total RNAs rather than small RNA-enriched samples, and chemiluminescence rather than radioactive detection, were used. Digoxigeninlabeled probes were generated by using the PCR DIG Probe Synthesis Kit (Roche Diagnostics).…”
Section: Dna/rna Extraction and Analysismentioning
confidence: 99%