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1.
J Gen Virol ; 88(Pt 10): 2852-2861, 2007 Oct.
Article in English | MEDLINE | ID: mdl-17872540

ABSTRACT

In vitro reverse transcription of a mixture of total RNA from plants infected with the I17F or R strains of cucumber mosaic virus (CMV), representative of subgroups IA and II, respectively, results in viral cDNA populations including rare recombinant RNA 3 molecules, some of which also have point mutations. The biological properties of 17 recombinants in the capsid gene or the 3' non-coding region of RNA 3 were evaluated when associated with I17F RNAs 1 and 2. Six viruses displayed deficiencies (non-viability, deficiencies for movement and/or replication, delayed infection, loss of aphid transmissibility). Nine induced symptoms close to those of I17F-CMV on tobacco and pepper plants. All recombinants bearing the movement protein (MP) of R-CMV and part or most of the capsid protein (CP) of I17F-CMV, as well as the recombinant created in vitro by exchanging the corresponding open reading frames, also induced filiformism on tobacco, but induced only faint symptoms on melon. Two recombinants induced atypically severe symptoms on both tobacco and pepper. Most of the recombinants generally accumulated to lower levels than the wild-type I17F strain in tobacco. Three recombinants, however, including one responsible for severe symptoms, accumulated to generally higher levels than I17F-CMV. When two of these were tested in co-infection experiments with I17F RNA 3, they proved to be poorly competitive, suggesting that they would be unlikely to emerge in the field.


Subject(s)
Cucumovirus/genetics , RNA, Viral/genetics , Recombination, Genetic , Cloning, Molecular , Cucumovirus/growth & development , Cucumovirus/isolation & purification , DNA, Complementary/genetics , Genetic Variation , Plant Diseases/virology , Plant Leaves/virology , Plant Viruses/genetics , Plasmids , RNA, Viral/isolation & purification , Nicotiana/virology
2.
Mol Genet Genomics ; 273(1): 10-9, 2005 Mar.
Article in English | MEDLINE | ID: mdl-15711971

ABSTRACT

A novel Arabidopsis thaliana gene (AtNADK-1) was identified based on its response to radiation and oxidative stress. Levels of AtNADK-1 mRNA increase eight-fold following exposure to ionising radiation and are enhanced three-fold by treatment with hydrogen peroxide. The gene also appears to be differentially regulated during compatible and incompatible plant-pathogen interactions in response to Pseudomonas syringae pv. tomato. The full-length AtNADK-1 cDNA encodes a 58-kDa protein that shows high sequence homology to the recently defined family of NAD(H) kinases. Recombinant AtNADK-1 utilises ATP to phosphorylate both NAD and NADH, showing a two-fold preference for NADH. Using reverse genetics, we demonstrate that AtNADK-1 deficient plants display enhanced sensitivity to gamma irradiation and to paraquat-induced oxidative stress. Our results indicate that this novel NAD(H) kinase may contribute to the maintenance of redox status in Arabidopsis thaliana.


Subject(s)
Arabidopsis Proteins/metabolism , Arabidopsis/genetics , Gene Expression Regulation, Plant/drug effects , Gene Expression Regulation, Plant/radiation effects , Oxidative Stress/genetics , Phosphotransferases (Alcohol Group Acceptor)/metabolism , Phosphotransferases/metabolism , Amino Acid Sequence , Anthocyanins/metabolism , Arabidopsis/metabolism , Arabidopsis/microbiology , Arabidopsis Proteins/genetics , Base Sequence , DNA Primers , DNA Transposable Elements/genetics , DNA, Complementary/genetics , Electrophoresis, Polyacrylamide Gel , Hydrogen Peroxide/pharmacology , Molecular Sequence Data , Phosphotransferases/genetics , Phosphotransferases (Alcohol Group Acceptor)/genetics , Pseudomonas syringae , Reverse Transcriptase Polymerase Chain Reaction , Sequence Alignment , Sequence Analysis, DNA
3.
J Virol Methods ; 121(2): 247-57, 2004 Nov.
Article in English | MEDLINE | ID: mdl-15381363

ABSTRACT

Reverse transcriptases with RNase H activity are particularly apt to switch templates and generate recombinant molecules in vitro. This property has been exploited for the first time to create a library of recombinant RNAs 3 between two strains of Cucumber mosaic virus (CMV) or between CMV and Tomato aspermy virus (TAV), which share 75 and 63% sequence identity, respectively. The recombination events were almost entirely of the precise homologous type, and occurred at the same sites as those previously identified in co-infected plants, making it possible to use this strategy to create numerous cDNA fragments with crossovers similar to those occurring in vivo. Sub-cloning of recombinant fragments into an infectious full-length clone was accomplished by homologous recombination in yeast, alleviating the need for in vitro ligation at common restriction sites. Most of the recombinant genomes were infectious. Association of these two methods constitutes an efficient and practical means for generating numerous infectious viral genomes equivalent to ones that might arise by precise homologous recombination between two parental viral genomes in nature.


Subject(s)
Cucumovirus/genetics , Genome, Viral , RNA, Viral/genetics , Recombination, Genetic , Base Sequence , Cloning, Molecular , DNA, Complementary/biosynthesis , DNA, Viral/biosynthesis , Molecular Sequence Data , RNA, Viral/biosynthesis , Sequence Alignment , Yeasts/genetics
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