Abstract
RNA silencing is a sequence-specific RNA degradation process that follows the recognition of double-stranded RNA.
Here, we show that virus vectors carrying parts of a green fluorescent protein (GFP) transgene targeted RNA silencing
in Nicotiana benthamiana and Arabidopsis against the entire GFP RNA. These results indicate that there was spreading
of RNA targeting from the initiator region into the adjacent 5'and 3' regions of the target gene. Spreading was accompanied by methylation of the corresponding GFP DNA. It also was dependent on transcription of the transgene and on the putative RNA-dependent RNA polymerase, SDE1/SGS2. These findings indicate that SDE1/SGS2 produces doublestranded
RNA using the target RNA as a template. RNA silencing of ribulose-1,5-bisphosphate carboxylase/oxygenase and phytoene desaturase was not associated with the spreading of RNA targeting or DNA methylation, indicating that these endogenous RNAs are not templates for SDE1/SGS2.
Original language | English |
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Pages (from-to) | 857-867 |
Number of pages | 10 |
Journal | The Plant Cell |
Volume | 14 |
Issue number | 4 |
DOIs | |
Publication status | Published - Apr 2002 |
Keywords
- Arabidopsis
- Arabidopsis Proteins
- DNA Methylation
- Gene Silencing
- Green Fluorescent Proteins
- Luminescent Proteins
- Oxidoreductases
- Plant Proteins
- Plants, Genetically Modified
- RNA Replicase
- RNA, Plant
- RNA-Induced Silencing Complex
- Ribonucleoproteins
- Ribulose-Bisphosphate Carboxylase
- Tobacco
- Transcription, Genetic