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J. Virol., Dec 1997, 9087-9095, Vol 71, No. 12
J Brunstein and CR Astell
Prior analysis of minigenomes of minute virus of mice carried out by our
laboratory indicated that sequences within the region of nucleotides 4489
to 4695, inboard of the 5' palindrome, are required for efficient DNA
replication of the virus and are the site of specific interactions with
unidentified factors present in a host cell nuclear extract (P. Tam and C.
R. Astell, Virology 193:812-824, 1993; P. Tam and C. R. Astell, J. Virology
68:2840-2848, 1994). In order to examine this region in finer detail, a
comprehensive library of linker-scanning mutants spanning the region was
tested for the ability to support replication of minigenome constructs and
for the ability to interact with host cell factors. Three short discrete
sequence elements critical for replication competence were observed.
Binding of host cell nuclear factors was localized to four sites, with two
major complexes each appearing to have two binding sites within the region.
All factor binding sites were found to be directly adjacent to or
overlapping with sequence elements contributing to replication competence,
and evidence suggesting a correlation between factor binding and minigenome
replication is presented. A possible model is proposed for function of a
viral origin within the region of the internal replication sequence which
addresses the still-unresolved problem of how parvoviruses overcome the
thermodynamic energy barrier involved in the rearrangement of the
5'-terminal palindrome from an extended form to a hairpin conformation.
Copyright © 1997, American Society for Microbiology
Analysis of the internal replication sequence indicates that there are three elements required for efficient replication of minute virus of mice minigenomes
Department of Biochemistry and Molecular Biology, Faculty of Medicine, University of British Columbia, Vancouver, Canada.
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