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THE PLANT CELL, Vol 5, Issue 5 577-586, Copyright © 1993 by American Society of Plant Biologists
Analysis of a Tobacco Mosaic Virus Strain Capable of Overcoming N Gene-Mediated Resistance
H. S. Padgett and R. N. Beachy
Division of Biology and Biomedical Sciences, Washington University, St. Louis, Missouri 63110
The genome of Ob, a tobamovirus that overcomes the N gene-mediated
hypersensitive response (HR), was cloned as a cDNA, and its nucleotide
sequence was determined. The genomic organization of Ob is similar to that
of other tobamoviruses, consisting of 6506 nucleotides and containing at
least four open reading frames. These open reading frames encode a 126-kD
polypeptide with a 183-kD readthrough product, a 30.6-kD movement protein,
and an 18-kD coat protein. A bacteriophage T7 promoter sequence was fused
to the full-length cDNA clone to obtain infectious RNA transcripts. These
transcripts, when inoculated onto tobacco plants, induced disease symptoms
indistinguishable from plants inoculated with Ob viral RNA. To determine
which viral factor is responsible for the resistance-breaking character of
Ob, a recombinant virus was constructed in which the movement protein gene
of tobacco mosaic virus was replaced with that of Ob. Cultivar Xanthi NN
tobacco plants infected with this virus responded with an HR, indicating
that the Ob movement protein alone does not act to overcome the N
gene-mediated response. Following mutagenesis of the infectious Ob cDNA
clone with hydroxylamine, populations of transcripts from the mutagenized
DNA were inoculated onto Xanthi NN tobacco, and a variant that induced the
HR was identified. The mutant was analyzed and found to contain a single
nucleotide change in the 126-kD gene. Recreating the mutation in the Ob
cDNA clone by site-directed mutagenesis resulted in a virus that caused
symptoms identical to the chemically induced mutant.
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