A novel genetic screen was used to identify host factors in Arabidopsis thaliana that suppress mutations in the Cauliflower mosaic virus (CaMV) movement protein gene (gene I). A series of small mutations was made in gene I and the mutations were tested for their suitability in a suppressor screen. The first round of screening yielded only revertants or second-site mutations in gene I. A derivative of one of the second-site mutant viruses (N7) that was delayed in symptom production was used in a second round of screening for suppressor plants that accelerated symptom production. Two candidate suppressor plants were found that accelerated by 1 to 4 days the first appearance of symptoms caused by the mutant viruses. One of the suppressors (5-2), called asci acceleration of symptoms by CaMV N7), was mapped to chromosome Two additional loci that differentially affect N7 virus susceptibility in the parental Columbia and Ler ecotypes were mapped to chromosomes 3 and 4 by quantitative trait locus (QTL) analysis.
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INRA CIRAD SupAgro, UMR BGPI 385, Equipe CaGeTE, Campus Int Baillarguet, Montpellier, France
Oxford Brookes Univ, Sch Life Sci, Oxford, EnglandINRA CIRAD SupAgro, UMR BGPI 385, Equipe CaGeTE, Campus Int Baillarguet, Montpellier, France
Martiniere, Alexandre
Zancarini, Anouk
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INRA CIRAD SupAgro, UMR BGPI 385, Equipe CaGeTE, Campus Int Baillarguet, Montpellier, France
INRA Dijon, UMR LEG Equipe Ecophysiol, Dijon, FranceINRA CIRAD SupAgro, UMR BGPI 385, Equipe CaGeTE, Campus Int Baillarguet, Montpellier, France
Zancarini, Anouk
Drucker, Martin
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INRA CIRAD SupAgro, UMR BGPI 385, Equipe CaGeTE, Campus Int Baillarguet, Montpellier, FranceINRA CIRAD SupAgro, UMR BGPI 385, Equipe CaGeTE, Campus Int Baillarguet, Montpellier, France