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Suppression of Virus Accumulation in Transgenic Plants Exhibiting Silencing of Nuclear Genes.
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/bf00039377openalex-snapshot
Control of mRNA stability in higher plants
inferredcites →https://doi.org/10.1007/bf00039425openalex-snapshot
The effect of T-DNA copy number, position and methylation on reporter gene expression in tobacco transformants
inferredcites →https://doi.org/10.1007/bf00039614openalex-snapshot
Transgene copy number can be positively or negatively associated with transgene expression
inferredcites →https://doi.org/10.1007/bf00262443openalex-snapshot
Expression of a truncated tomato polygalacturonase gene inhibits expression of the endogenous gene in transgenic plants
inferredcites →https://doi.org/10.1007/bf00285449openalex-snapshot
Homology-dependent gene silencing in transgenic plants: epistatic silencing loci contain multiple copies of methylated transgenes
inferredcites →https://doi.org/10.1007/bf02667740openalex-snapshot
Assaying chimeric genes in plants: The GUS gene fusion system
inferredcites →https://doi.org/10.1016/0042-6822(92)90584-copenalex-snapshot
Molecular analysis of a resistance-breaking strain of potato virus X
inferredcites →https://doi.org/10.1016/0092-8674(94)90119-8openalex-snapshot
RNA-directed de novo methylation of genomic sequences in plants
inferredcites →https://doi.org/10.1016/0167-7799(90)90220-ropenalex-snapshot
Altered gene expression in plants due totrans interactions between homologous genes
inferredcites →https://doi.org/10.1046/j.1365-313x.1992.t01-24-00999.xopenalex-snapshot
Potato virus X as a vector for gene expression in plants
inferredcites →https://doi.org/10.1046/j.1365-313x.1993.04010089.xopenalex-snapshot
Differences in DNA‐methylation are associated with a paramutation phenomenon in transgenic petunia
inferredcites →https://doi.org/10.1046/j.1365-313x.1994.6060861.xopenalex-snapshot
Transgene‐mediated suppression of chalcone synthase expression in Petunia hybrida results from an increase in RNA turnover
inferredcites →https://doi.org/10.1046/j.1365-313x.1995.07061001.xopenalex-snapshot
Homology‐dependent resistance: transgenic virus resistance in plants related to homology‐dependent gene silencing
inferredcites →https://doi.org/10.1046/j.1365-313x.1995.07061045.xopenalex-snapshot
Jellyfish green fluorescent protein as a reporter for virus infections
inferredcites →https://doi.org/10.1073/pnas.82.9.2560openalex-snapshot
Effect of regional DNA methylation on gene expression.
inferredcites →https://doi.org/10.1073/pnas.90.10.4557openalex-snapshot
Methylation induced premeiotically in Ascobolus: coextension with DNA repeat lengths and effect on transcript elongation.
inferredcites →https://doi.org/10.1073/pnas.91.12.5538openalex-snapshot
Identification of plant genetic loci involved in a posttranscriptional mechanism for meiotically reversible transgene silencing.
inferredcites →https://doi.org/10.1073/pnas.91.22.10502openalex-snapshot
Posttranscriptional silencing of reporter transgenes in tobacco correlates with DNA methylation.
inferredcites →https://doi.org/10.1073/pnas.91.9.3490openalex-snapshot
Inactivation of gene expression in plants as a consequence of specific sequence duplication.
inferredcites →https://doi.org/10.1093/nar/14.21.8595openalex-snapshot
Sequencing and identification of a cDNA done for tomato polygalacturonase
inferredcites →https://doi.org/10.1104/pp.102.4.1065openalex-snapshot
Control of mRNA Stability in Higher Plants
inferredcites →https://doi.org/10.1104/pp.107.3.679openalex-snapshot
How and Why Do Plants Inactivate Homologous (Trans)genes?
inferredcites →https://doi.org/10.1105/tpc.2.4.279openalex-snapshot
Introduction of a Chimeric Chalcone Synthase Gene into Petunia Results in Reversible Co-Suppression of Homologous Genes in trans.
inferredcites →https://doi.org/10.1105/tpc.2.4.291openalex-snapshot
Flavonoid genes in petunia: addition of a limited number of gene copies may lead to a suppression of gene expression.
inferredcites →https://doi.org/10.1105/tpc.5.12.1749openalex-snapshot
Induction of a Highly Specific Antiviral State in Transgenic Plants: Implications for Regulation of Gene Expression and Virus Resistance.
inferredcites →https://doi.org/10.1105/tpc.5.6.667openalex-snapshot
An Arabidopsis mutant with a reduced level of cab140 RNA is a result of cosuppression.
inferredcites →https://doi.org/10.1105/tpc.6.10.1441openalex-snapshot
Transgenic plant virus resistance mediated by untranslatable sense RNAs: expression, regulation, and fate of nonessential RNAs.
inferredcites →https://doi.org/10.1105/tpc.7.3.347openalex-snapshot
Post-transcriptional cosuppression of beta-1,3-glucanase genes does not affect accumulation of transgene nuclear mRNA.
inferredcites →https://doi.org/10.1126/science.8303295openalex-snapshot
Green Fluorescent Protein as a Marker for Gene Expression
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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RNA Silencing and its Suppressors in the Plant‐virus Interplay
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Transgene‐Promoted Epigenetic Switches of Chalcone Synthase Activity in Petunia Plants
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inferred← citeshttps://doi.org/10.1007/978-94-011-4183-3_9openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-94-011-5596-0_19openalex-snapshot
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Breeding Forage Plants in the Genome Era
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Plant DNA Methylation and Gene Expression
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Overcoming and Exploiting RNA Silencing
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GM Crops for Plant Virus Resistance: A Review
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Begomovirus Interaction with Ornamental Plants: Recent Advances and Methods for Engineering Resistance
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Co-suppression of the hydrophobin gene HCf-1 is correlated with antisense RNA biosynthesis in Cladosporium fulvum
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Cross‐talk between posttranscriptionally silenced neomycin phosphotransferase II transgenes
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Drug‐induced hypomethylation of a posttranscriptionally silenced transgene locus of tobacco leads to partial release of silencing
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Transformation and gene expression
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Replicase-Mediated Resistance to Plant Virus Disease
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Cosuppression Comes to the Animals
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RNA-Mediated RNA Degradation and Chalcone Synthase A Silencing in Petunia
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Commercialization of Genetically Engineered Potato Plants Resistant to Disease
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Delayed activation of post-transcriptional gene silencing and de novo transgene methylation in plants with the coat protein gene of sweet potato feathery mottle potyvirus
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Des pruniers résistant à la maladie de la sharka
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Plum pox potyvirus resistance associated to transgene silencing that can be stabilized after different number of plant generations
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Post-transcriptional gene silencing in plants
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Ectopic pairing of homologous DNA and post-transcriptional gene silencing in transgenic plants
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RNA-directed transcriptional gene silencing in plants can be inherited independently of the RNA trigger and requires Met1 for maintenance
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Viral suppression of systemic silencing
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Internuclear Gene Silencing in Phytophthora infestans
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Gene silencing and virus resistance: a common mechanism
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Virus-induced gene silencing in infected and transgenic plants
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Conservation of transgene-induced post-transcriptional gene silencing in plants and fungi
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Virus resistance and gene silencing: killing the messenger
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Controlling gene expression in transgenics
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Fast forward genetics based on virus-induced gene silencing
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Gene Silencing as a Tool for the Identification of Gene Function in Fungi
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RNAi and gene silencing phenomena mediated by viral suppressors in plants
inferred← citeshttps://doi.org/10.1017/s1355838200001096openalex-snapshot
Detailed characterization of the posttranscriptional gene-silencing-related small RNA in a GUS gene-silenced tobacco
inferred← citeshttps://doi.org/10.1017/s135583820099201xopenalex-snapshot
A DNA target of 30 bp is sufficient for RNA-directed DNA methylation
inferred← citeshttps://doi.org/10.1017/s1355838202026080openalex-snapshot
Specific degradation of 3??? regions of GUS mRNA in posttranscriptionally silenced tobacco lines may be related to 5???-3??? spreading of silencing
inferred← citeshttps://doi.org/10.1017/s1355838299990799openalex-snapshot
Posttranscriptional gene silencing of gn1 in tobacco triggers accumulation of truncated gn1-derived RNA species
inferred← citeshttps://doi.org/10.1023/a:1005882106266openalex-snapshot
Silencing of a β-1,3-glucanase transgene is overcome during seed formation
inferred← citeshttps://doi.org/10.1023/a:1005946720438openalex-snapshot
A model for RNA-mediated gene silencing in higher plants
inferred← citeshttps://doi.org/10.1023/a:1006364323494openalex-snapshot
Expression and sequence requirements for nitrite reductase co–suppression
inferred← citeshttps://doi.org/10.1023/a:1006408101473openalex-snapshot
Plant DNA viruses and gene silencing
inferred← citeshttps://doi.org/10.1023/a:1006412318311openalex-snapshot
Transgene silencing in monocots
inferred← citeshttps://doi.org/10.1023/a:1006443731515openalex-snapshot
RNA degradation and models for post-transcriptional gene silencing
inferred← citeshttps://doi.org/10.1023/a:1006456000564openalex-snapshot
RNA viruses as inducers, suppressors and targets of post-transcriptional gene silencing
inferred← citeshttps://doi.org/10.1023/a:1006456603970openalex-snapshot
Expression of a yeast RNase III gene in transgenic tobacco silences host nitrite reductase genes
inferred← citeshttps://doi.org/10.1023/a:1006464304199openalex-snapshot
Plants as bioreactors for protein production: avoiding the problem of transgene silencing
inferred← citeshttps://doi.org/10.1023/a:1006490331303openalex-snapshot
High-efficiency silencing of a β-glucuronidase gene in rice is correlated with repetitive transgene structure but is independent of DNA methylation
inferred← citeshttps://doi.org/10.1023/a:1006491613768openalex-snapshot
Role of inverted DNA repeats in transcriptional and post-transcriptional gene silencing
inferred← citeshttps://doi.org/10.1023/a:1008806911748openalex-snapshot
Complete resistance to pepper mild mottle tobamovirus mediated by viral replicase sequences partially depends on transgene homozygosity and is based on a gene silencing mechanism
inferred← citeshttps://doi.org/10.1023/a:1008851821374openalex-snapshot
High resistance to plum pox virus (PPV) in transgenic plants containing modified and truncated forms of PPV coat protein gene
inferred← citeshttps://doi.org/10.1023/a:1008915007271openalex-snapshot
Turnip mosaic potyvirus resistance in Nicotiana benthamiana derived by post‐transcriptional gene silencing
inferred← citeshttps://doi.org/10.1023/a:1009613607559openalex-snapshot
Transgenic beans (Phaseolus vulgaris L.) engineered to express viral antisense RNAs show delayed and attenuated symptoms to bean golden mosaic geminivirus
inferred← citeshttps://doi.org/10.1023/a:1009633816713openalex-snapshot
Rice plant (Oryza sativa L.) containing Rice tungro spherical virus (RTSV) coat protein transgenes are resistant to virus infection
inferred← citeshttps://doi.org/10.1023/a:1009671925550openalex-snapshot
Coat protein gene-mediated protection in Lactuca sativa against lettuce mosaic potyvirus strains
inferred← citeshttps://doi.org/10.1023/a:1012226319449openalex-snapshot
Recent advances in molecular genetics of forest trees
inferred← citeshttps://doi.org/10.1023/a:1015656017326openalex-snapshot
Tobacco Plants Transformed with an Untranslatable Form of the Coat Protein Gene of the Potato Virus Y are Resistant to Viral Infection
inferred← citeshttps://doi.org/10.1023/a:1016644823203openalex-snapshot
Post-transcriptional gene silencing in plum pox virus resistant transgenic European plum containing the plum pox potyvirus coat protein gene
inferred← citeshttps://doi.org/10.1023/a:1022410823525openalex-snapshot
Coat protein-mediated resistance to Turnip mosaic virus in oilseed rape (Brassica napus)
inferred← citeshttps://doi.org/10.1023/a:1026576124482openalex-snapshot
Resistance to wheat streak mosaic virus in transgenic wheat expressing the viral replicase (NIb) gene
inferred← citeshttps://doi.org/10.1023/b:molb.0000022527.68551.30openalex-snapshot
Transgene silencing in Phalaenopsis expressing the coat protein of Cymbidium Mosaic Virus is a manifestation of RNA-mediated resistance
inferred← citeshttps://doi.org/10.1023/b:molb.0000047769.82881.f5openalex-snapshot
High frequency induction of RNA-mediated resistance against Cucumber mosaic virus using inverted repeat constructs
inferred← citeshttps://doi.org/10.1034/j.1399-3054.1999.100113.xopenalex-snapshot
Developmental timing of transgene expression is dosage dependent
inferred← citeshttps://doi.org/10.1038/35081168openalex-snapshot
Gene silencing as an adaptive defence against viruses
inferred← citeshttps://doi.org/10.1038/5997openalex-snapshot
Taming of transposable elements by homology-dependent gene silencing
inferred← citeshttps://doi.org/10.1038/nature02107openalex-snapshot
Transposon silencing in the Caenorhabditis elegans germ line by natural RNAi
inferred← citeshttps://doi.org/10.1038/nm1008-1046openalex-snapshot
Of maize and men, or peas and people: case histories to justify plants and other model systems
inferred← citeshttps://doi.org/10.1038/sj.onc.1208072openalex-snapshot
Oncology studies using siRNA libraries: the dawn of RNAi-based genomics
inferred← citeshttps://doi.org/10.1046/j.1365-2540.2001.00799.xopenalex-snapshot
Breeding virus resistant potatoes (Solanum tuberosum): a review of traditional and molecular approaches
inferred← citeshttps://doi.org/10.1046/j.1365-2583.2001.00267.xopenalex-snapshot
Sindbis virus‐induced silencing of dengue viruses in mosquitoes
inferred← citeshttps://doi.org/10.1046/j.1365-2958.2003.03878.xopenalex-snapshot
Let there be blight: functional analysis of virulence in Phytophthora infestans
inferred← citeshttps://doi.org/10.1046/j.1365-313x.1997.12051127.xopenalex-snapshot
Post‐transcriptional gene silencing of ACC synthase in tomato results from cytoplasmic RNA degradation
inferred← citeshttps://doi.org/10.1046/j.1365-313x.1998.00038.xopenalex-snapshot
Distinct patterns of pigment suppression are produced by allelic sense and antisense chalcone synthase transgenes in petunia flowers
inferred← citeshttps://doi.org/10.1046/j.1365-313x.1998.00053.xopenalex-snapshot
Pathogen‐derived resistance targeted against the negative‐strand RNA of tobacco mosaic virus: RNA strand‐specific gene silencing?
inferred← citeshttps://doi.org/10.1046/j.1365-313x.1998.00101.xopenalex-snapshot
Gene silencing from plant DNA carried by a Geminivirus
inferred← citeshttps://doi.org/10.1046/j.1365-313x.1998.00157.xopenalex-snapshot
Post‐transcriptional silencing of pectin methylesterase gene in transgenic tomato fruits results from impaired pre‐mRNA processing
inferred← citeshttps://doi.org/10.1046/j.1365-313x.1998.00211.xopenalex-snapshot
Post‐transcriptional silencing of chalcone synthase in petunia using a geminivirus‐based episomal vector
inferred← citeshttps://doi.org/10.1046/j.1365-313x.1998.00251.xopenalex-snapshot
A transgene with repeated DNA causes high frequency, post‐transcriptional suppression of ACC‐oxidase gene expression in tomato
inferred← citeshttps://doi.org/10.1046/j.1365-313x.1998.00337.xopenalex-snapshot
Transgene‐induced gene silencing in plants
inferred← citeshttps://doi.org/10.1046/j.1365-313x.1999.00373.xopenalex-snapshot
Silencing of an aleurone‐specific gene in transgenic rice is caused by a rearranged transgene
inferred← citeshttps://doi.org/10.1046/j.1365-313x.1999.00419.xopenalex-snapshot
The interaction between plastocyanin and photosystem I is inefficient in transgenic Arabidopsis plants lacking the PSI‐N subunit of photosystem
inferred← citeshttps://doi.org/10.1046/j.1365-313x.1999.00425.xopenalex-snapshot
Post‐transcriptional gene silencing of chalcone synthase in transgenic petunias, cytosine methylation and epigenetic variation
inferred← citeshttps://doi.org/10.1046/j.1365-313x.1999.00582.xopenalex-snapshot
Sequences throughout the basic β‐1,3‐glucanase mRNA coding region are targets for homology dependent post‐transcriptional gene silencing
inferred← citeshttps://doi.org/10.1046/j.1365-313x.2000.00645.xopenalex-snapshot
Graft transmission of post‐transcriptional gene silencing: target specificity for RNA degradation is transmissible between silenced and non‐silenced plants, but not between silenced plants
inferred← citeshttps://doi.org/10.1046/j.1365-313x.2000.00710.xopenalex-snapshot
Plant viral suppressors of post‐transcriptional silencing do not suppress transcriptional silencing
inferred← citeshttps://doi.org/10.1046/j.1365-313x.2001.00976.xopenalex-snapshot
Size constraints for targeting post‐transcriptional gene silencing and for RNA‐directed methylation in Nicotiana benthamiana using a potato virus X vector
inferred← citeshttps://doi.org/10.1046/j.1365-313x.2001.01079.xopenalex-snapshot
Inducible high‐level mRNA amplification system by viral replicase in transgenic plants
inferred← citeshttps://doi.org/10.1046/j.1365-313x.2002.01236.xopenalex-snapshot
Relationship between small antisense RNAs and aberrant RNAs associated with sense transgene mediated gene silencing in tomato
inferred← citeshttps://doi.org/10.1046/j.1365-313x.2003.01659.xopenalex-snapshot
Inverted repeat of a heterologous 3′‐untranslated region for high‐efficiency, high‐throughput gene silencing
inferred← citeshttps://doi.org/10.1046/j.1365-313x.2003.01785.xopenalex-snapshot
The capacity of transgenic tobacco to send a systemic RNA silencing signal depends on the nature of the inducing transgene locus
inferred← citeshttps://doi.org/10.1046/j.1469-8137.2002.00467.xopenalex-snapshot
Progression of geminivirus‐induced transgene silencing is associated with transgene methylation
inferred← citeshttps://doi.org/10.1071/pp98121openalex-snapshot
The maize transcription factor Sn alters proanthocyanidin synthesis in transgenic Lotus corniculatus plants
inferred← citeshttps://doi.org/10.1073/pnas.0404940101openalex-snapshot
Three distinct suppressors of RNA silencing encoded by a 20-kb viral RNA genome
inferred← citeshttps://doi.org/10.1073/pnas.0606536103openalex-snapshot
Defective RNA processing enhances RNA silencing and influences flowering of Arabidopsis
inferred← citeshttps://doi.org/10.1073/pnas.200217597openalex-snapshot
AGO1, QDE-2, and RDE-1 are related proteins required for post-transcriptional gene silencing in plants, quelling in fungi, and RNA interference in animals
inferred← citeshttps://doi.org/10.1073/pnas.94.15.8261openalex-snapshot
Nontarget DNA sequences reduce the transgene length necessary for RNA-mediated tospovirus resistance in transgenic plants
inferred← citeshttps://doi.org/10.1073/pnas.94.19.10233openalex-snapshot
Isolation of quelling-defective ( qde ) mutants impaired in posttranscriptional transgene-induced gene silencing in Neurospora crassa
inferred← citeshttps://doi.org/10.1073/pnas.95.16.9675openalex-snapshot
Transgenes are dispensable for the RNA degradation step of cosuppression
inferred← citeshttps://doi.org/10.1073/pnas.95.22.13079openalex-snapshot
A viral suppressor of gene silencing in plants
inferred← citeshttps://doi.org/10.1073/pnas.95.23.13349openalex-snapshot
Plant gene silencing regularized
inferred← citeshttps://doi.org/10.1073/pnas.95.23.13959openalex-snapshot
Virus resistance and gene silencing in plants can be induced by simultaneous expression of sense and antisense RNA
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