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Genetic resistances to plant viruses and their vectors

Bibliographic Reference from DPPMA-UNIBA
Department of Plant Protection and Applied Microbiology - UNIBA
Bari - Italy

More data about this group.

Last database update for these data: 2006-12-20 - Data extracted on 2009-04-14 from the database.

Generation of siRNAs by T-DNA sequences does not require active transcription or homology to sequences in the plant

Bibliographic Reference
Field Value
Document typeJournal article: paper
LanguageEnglish
Year2002
AuthorsCanto, T.
Cillo, F.
Palukaitis, P.
TitleGeneration of siRNAs by T-DNA sequences does not require active transcription or homology to sequences in the plant
SourceMol. Plant Microbe Interact.
Volume15
Issue11
Pages1137-1146
AbstractDelivery into plants of T-DNAs containing promoter, terminator, or coding sequences generated small interfering RNAs (siRNAs) specific to each type of sequence. When both promoter and transcribed sequences were simultaneously present in the T-DNA, accumulation of siRNAs to transcribed sequences was favored over accumulation of siRNAs to the nontranscribed upstream promoter sequences. The generation of specific siRNA sequences occurred even in the absence of T-DNA homology to sequences in the plant. Delivery of T-DNA, with homology to the transgene limited to the nontranscribed cauliflower mosaic virus 35S promoter (35SP) and the transcribed nopaline synthase transcription termination (NosT)signal sequences, into transgenic plants expressing the green fluorescent protein (GFP), generated siRNAs in infiltrated tissues to both 35SP (35SsiRNAs) and NosT (NosTsiRNAs), but not to the GFP sequence (GFPsiRNAs). In infiltrated tissues, the 35SsiRNAs failed to trigger the transcriptional silencing of the transgene, accumulation of 35SsiRNAs could be prevented by the potyviral HC-Pro, and the NosTsiRNAs required an initial amplification to trigger efficient transgene silencing, which is mediated by transcripts from the exogenous T-DNA, and not from the transgene. In upper leaves, silencing correlated with the presence of GFPsiRNAs and the absence of 35SsiRNAs, confirming that its spread was posttranscriptionally mediated by the transgene mRNA.
Web pagePubmed
ISSN0894-0282
DescriptorsAmino Acid Oxidoreductases genetics
Caulimovirus genetics
Bacteria DNA genetics and metabolism
Plant DNA genetics
Plant Gene Expression Regulation
Green Fluorescent Proteins
Luminescent Proteins genetics and metabolism
Plants genetics
Genetically Modified Plants
Protein Sorting Signals genetics
RNA Interference
Small Interfering RNA biosynthesis and genetics
Recombinant Fusion Proteins genetics and metabolism
Rhizobium radiobacter genetics
Tobacco genetics
Trans-Activation (Genetics)