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J Gen Virol 71 (1990), 1403-1407; DOI 10.1099/0022-1317-71-6-1403
© 1990 Society for General Microbiology

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Use of Chenopodium hybridium facilitates isolation of brome mosaic virus RNA recombinants

A. L. N. Rao, Brian P. Sullivan and Timothy C. Hall

Department of Biology, Texas A&M University, College Station, Texas 77843-3258, U.S.A.

Three mutant brome mosaic virus (BMV) RNA-2 transcripts bearing two alterations in the pseudoknot region and one in arm C of the 3' tRNA region, previously characterized as being deficient in tRNA-like functions, have been assayed for their ability to infect and replicate (in the presence of wild-type RNAs-1 and -3) in Chenopodium hybridum plants. Although the introduced mutations have been shown to incapacitate the replication of RNA-2 in barley protoplasts, C. hybridum plants inoculated with these mutants developed local lesions indistinguishable in appearance and morphology from control inoculations containing wild-type RNA-2. Sequence analysis of progeny RNA-2 from two single lesion isolates for each mutant inoculum revealed that the input mutations were restored to functional sequences by homologous recombination within the 3' tRNA-like region. These results, which reflect the ease with which progeny RNA can be characterized from single lesions, exemplify the value of C. hybridum for studying recombination among viral RNAs.

Received 27 November 1989; accepted 22 February 1990.


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