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Journal of Virology, May 1999, p. 3638-3648, Vol. 73, No. 5
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Sequence and Structural Elements at the 3' Terminus
of Bovine Viral Diarrhea Virus Genomic RNA: Functional Role during
RNA Replication
Haiying
Yu,
Claus W.
Grassmann, and
Sven-Erik
Behrens*
Institut für Virologie (FB
Veterinärmedizin), Justus-Liebig-Universität Giessen,
D-35392 Giessen, Germany
Received 18 September 1998/Accepted 19 January 1999
Bovine viral diarrhea virus (BVDV), a member of the genus
Pestivirus in the family Flaviviridae, has a
positive-stranded RNA genome consisting of a single open reading frame
and untranslated regions (UTRs) at the 5' and 3' ends. Computer
modeling suggested the 3' UTR comprised single-stranded regions as well
as stem-loop structures
features that were suspected of being
essentially implicated in the viral RNA replication pathway. Employing
a subgenomic BVDV RNA (DI9c) that was shown to function as an
autonomous RNA replicon (S.-E. Behrens, C. W. Grassmann, H. J. Thiel, G. Meyers, and N. Tautz, J. Virol. 72:2364-2372, 1998)
the goal of this study was to determine the RNA secondary structure of
the 3' UTR by experimental means and to investigate the significance of
defined RNA motifs for the RNA replication pathway. Enzymatic and
chemical structure probing revealed mainly the conserved terminal part
(termed 3'C) of the DI9c 3' UTR containing distinctive RNA motifs,
i.e., a stable stem-loop, SL I, near the RNA 3' terminus and a
considerably less stable stem-loop, SL II, that forms the 5' portion of
3'C. SL I and SL II are separated by a long single-stranded intervening sequence, denoted SS. The 3'-terminal four C residues of the viral RNA
were confirmed to be single stranded as well. Other intramolecular interactions, e.g., with upstream DI9c RNA sequences, were not detected
under the experimental conditions used. Mutagenesis of the DI9c RNA
demonstrated that the SL I and SS motifs do indeed play essential roles
during RNA replication. Abolition of RNA stems, which ought to maintain
the overall folding of SL I, as well as substitution of certain
single-stranded nucleotides located in the SS region or SL I loop
region, gave rise to DI9c derivatives unable to replicate. Conversely,
SL I stems comprising compensatory base exchanges turned out to support
replication, but mostly to a lower degree than the original structure.
Surprisingly, replacement of a number of residues, although they were
previously defined as constituents of a highly conserved stretch of
sequence of the SS motif, had little effect on the replication ability
of DI9c. In summary, these results indicate that RNA structure as well as sequence elements harbored within the 3'C region of the BVDV 3' UTR
create a common cis-acting element of the replication
process. The data further point at possible interaction sites of host
and/or viral proteins and thus provide valuable information for future experiments intended to identify and characterize these factors.
*
Corresponding author. Mailing address: Institut
für Virologie (FB Veterinärmedizin),
Justus-Liebig-Universität Giessen, Frankfurter Str. 107, D-35392
Giessen, Germany. Phone: 496419938350. Fax: 496419938359. E-mail:
Sven-Erik.Behrens{at}vetmed.uni-giessen.de.
Journal of Virology, May 1999, p. 3638-3648, Vol. 73, No. 5
0022-538X/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
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