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Journal of Virology, November 2006, p. 10879-10883, Vol. 80, No. 21
0022-538X/06/$08.00+0 doi:10.1128/JVI.01501-06
Copyright © 2006, American Society for Microbiology. All Rights Reserved.
Susan F. Cotmore,1 and
Peter Tattersall1,2*
Departments of Laboratory Medicine,1 Genetics, Yale University Medical School, 333 Cedar Street, New Haven, Connecticut 0675102
Received 13 July 2006/ Accepted 11 August 2006
During DNA replication, the hairpin telomeres of Minute Virus of Mice (MVM) are extended and copied to create imperfectly palindromic duplex junction sequences that bridge adjacent genomes in concatameric replicative-form DNA. These are resolved by the viral initiator protein, NS1, but mechanisms employed at the two telomeres differ. Left-end:left-end junctions are resolved asymmetrically at a single site, OriLTC, by NS1 acting in concert with a host factor, parvovirus initiation factor (PIF). Replication segregates doublet and triplet sequences, initially present as unpaired nucleotides in the bubble region of the left-end hairpin stem, to either side of the junction. These act as spacers between the NS1 and PIF binding sites, and their asymmetric distribution sets up active (OriLTC) and inactive (OriLGAA) forms of OriL. We used a reverse genetic approach to disrupt this asymmetry and found that neither opposing doublets nor triplets in the hairpin bubble were tolerated. Viable mutants were isolated at low frequency and found to contain second-site mutations that either restored the asymmetry or crippled one PIF binding site. These mutations either inactivated the inboard or activated the outboard form of OriL, a polarity that strongly suggests that, in the genus Parvovirus, an active inboard OriL is lethal.
Published ahead of print on 23 August 2006.
Present address: Lawrence Livermore National Laboratory, Livermore, CA 94551.
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