Abstract
Partial denaturation mapping, restriction endonuclease digestion, and electron microscopy were used to determine which end of the linear duplex replicative-form (RF) DNA molecule contains the origin of RF replication for the parvovirus H-1. This origin was localized within approximately 300 base pairs of the arbitrarily designated right end of the RF DNA, in the EcoRI or HaeII-A fragment. Based on denaturation behavior in formamide, the right end was also found to have a relatively high guanine plus cytosine content, whereas the region adjacent to the left terminus of the RF DNA molecule was adenine plus thymine rich.
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- Blüthmann H., Brück D., Hübner L., Schöffski A. Reassociation of nucleic acids in solutions containing formamide. Biochem Biophys Res Commun. 1973 Jan 4;50(1):91–97. doi: 10.1016/0006-291x(73)91068-1. [DOI] [PubMed] [Google Scholar]
- Carter B. J., Koczot F. J., Garrison J., Rose J. A., Dolin R. Separate helper functions provided by adenovirus for adenovirus-associated virus multiplication. Nat New Biol. 1973 Jul 18;244(133):71–73. doi: 10.1038/newbio244071a0. [DOI] [PubMed] [Google Scholar]
- Davis R. W., Hyman R. W. A study in evolution: the DNA base sequence homology between coliphages T7 and T3. J Mol Biol. 1971 Dec 14;62(2):287–301. doi: 10.1016/0022-2836(71)90428-1. [DOI] [PubMed] [Google Scholar]
- Goldstein L., Thomas M., Davis R. W. EcoRI endonuclease cleavage map of bacteriophage P4-DNA. Virology. 1975 Aug;66(2):420–427. doi: 10.1016/0042-6822(75)90214-7. [DOI] [PubMed] [Google Scholar]
- Inman R. B., Schnös M. Partial denaturation of thymine- and 5-bromouracil-containing lambda DNA in alkali. J Mol Biol. 1970 Apr 14;49(1):93–98. doi: 10.1016/0022-2836(70)90378-5. [DOI] [PubMed] [Google Scholar]
- Jacob R. J., Lebowitz J., Kleinschmidt A. K. Locating interrupted hydrogen bonding in the secondary structure of PM2 circular DNA by comparative denaturation mapping. J Virol. 1974 Jun;13(6):1176–1185. doi: 10.1128/jvi.13.6.1176-1185.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Koczot F. J., Carter B. J., Garon C. F., Rose J. A. Self-complementarity of terminal sequences within plus or minus strands of adenovirus-associated virus DNA. Proc Natl Acad Sci U S A. 1973 Jan;70(1):215–219. doi: 10.1073/pnas.70.1.215. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rhode S. L., 3rd Replication process of the parvovirus H-1. VI. Characterization of a replication terminus of H-1 replicative-form DNA. J Virol. 1977 Feb;21(2):694–712. doi: 10.1128/jvi.21.2.694-712.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Singer I. I., Rhode S. L., 3rd Replication process of the parvovirus H-1. VII. Electron microscopy of replicative-form DNA synthesis. J Virol. 1977 Feb;21(2):713–723. doi: 10.1128/jvi.21.2.713-723.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Straus S. E., Sebring E. D., Rose J. A. Concatemers of alternating plus and minus strands are intermediates in adenovirus-associated virus DNA synthesis. Proc Natl Acad Sci U S A. 1976 Mar;73(3):742–746. doi: 10.1073/pnas.73.3.742. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wolfson J., Dressler D., Magazin M. Bacteriophage T7 DNA replication: a linear replicating intermediate (gradient centrifugation-electron microscopy-E. coli-DNA partial denaturation). Proc Natl Acad Sci U S A. 1972 Feb;69(2):499–504. doi: 10.1073/pnas.69.2.499. [DOI] [PMC free article] [PubMed] [Google Scholar]