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Journal of Virology, November 2000, p. 10323-10331, Vol. 74, No. 22
0022-538X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Recognition of the Core RNA Promoter for Minus-Strand RNA
Synthesis by the Replicases of Brome Mosaic Virus and
Cucumber Mosaic Virus
K.
Sivakumaran,1
Y.
Bao,2
M. J.
Roossinck,2 and
C. C.
Kao1,*
Department of Biology, Indiana University,
Bloomington, Indiana 47405,1 and
Noble Foundation, Ardmore, Oklahoma
734022
Received 7 July 2000/Accepted 21 August 2000
Replication of viral RNA genomes requires the specific interaction
between the replicase and the RNA template. Members of the
Bromovirus and Cucumovirus genera have a
tRNA-like structure at the 3' end of their genomic RNAs that interacts
with the replicase and is required for minus-strand synthesis. In
Brome mosaic virus (BMV), a stem-loop structure named C
(SLC) is present within the tRNA-like region and is required for
replicase binding and initiation of RNA synthesis in vitro. We have
prepared an enriched replicase fraction from tobacco plants infected
with the Fny isolate of Cucumber mosaic virus (Fny-CMV)
that will direct synthesis from exogenously added templates. Using this
replicase, we demonstrate that the SLC-like structure in Fny-CMV plays
a role similar to that of BMV SLC in interacting with the CMV
replicase. While the majority of CMV isolates have SLC-like elements
similar to that of Fny-CMV, a second group displays sequence or
structural features that are distinct but nonetheless recognized by
Fny-CMV replicase for RNA synthesis. Both motifs have a 5'CA3'
dinucleotide that is invariant in the CMV isolates examined, and
mutational analysis indicates that these are critical for interaction
with the replicase. In the context of the entire tRNA-like element,
both CMV SLC-like motifs are recognized by the BMV replicase. However,
neither motif can direct synthesis by the BMV replicase in the absence
of other tRNA-like elements, indicating that other features of the CMV tRNA can induce promoter recognition by a heterologous replicase.
*
Corresponding author. Mailing address: Department of
Biology, Indiana University, Bloomington, IN 47405. Phone: (812)
855-7959. Fax: (812) 855-6705. E-mail:
ckao{at}bio.indiana.edu.
Journal of Virology, November 2000, p. 10323-10331, Vol. 74, No. 22
0022-538X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
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