Abstract
Late in the life cycle of the single-stranded DNA phage phi X, the synthesis of positive strand DNA is coupled to the maturation of progeny virions. DNA synthesis and packaging take place in a replication-assembly complex, which we have purified to homogeneity and characterized. The following conclusions can be drawn: 1. The DNA component of the replication-assembly complex is a rolling circle with a single-stranded DNA tail which is less than or equal to genome length. 2. The major protein component of the replication-assembly complex is an intact viral capsid, as shown by gel analysis of 35S-labeled complexes. As replication proceeds at the DNA growing point, the positive strand tail of the rolling circle is displaced directly into the capsid. In addition to the capsid, the complex contains at least 1 molecule of the phi X gene A nicking protein, which appears to be covalently linked to the DNA. 3. The rolling circle . capsid complex can be purified to homogeneity by taking advantage of its uniform sedimentation velocity (35 S) and its uniform density upon equilibrium centrifugation in CsCl (1.50 g/cc). 4. The replication-assembly complex can be visualized in the electron microscope. An electron-dense particle, which has the dimensions of a viral capsid, is observed attached to a rolling circle at the DNA growing point. 5. Hybridization of specific phi X restriction fragments to the deproteinized, single-stranded tails of intact rolling circles has allowed the use of these replicating intermediates to determine both the origin/terminus and the direction of phi X positive strand DNA synthesis. The ends of the rolling circle tails map in the Hae III restriction Fragment Z6b, at the position on the phi X genome at which the gene A endonuclease is known to cut. This result indicates that this endonuclease participates in the "termination" of each round of synthesis by cutting off unit-length viral genomes. 6. Rolling circle . capsid complexes were also isolated from two other icosahedral, single-stranded DNA phages: G4 and St-1. The rolling circle . capsid complex seen in the case of the single-stranded DNA phages represents the first example of a structure in which DNA synthesis and viral assembly occur in a coupled manner. This tight coordination explains why double-stranded DNA circles are the net product of synthesis early in the viral life cycle while only single-stranded DNA circles are produced later. The single-stranded tails of the rolling circle intermediates are available for conversion to the duplex state at early times, whereas the concentration of preformed capsids later is high enough to bind to all of the replicating molecules and package the emerging positive strand DNA.
Highlights
- RESULTSPositive strand synthesisin the small, single-stranded DNA phages takes place in a rolling circle intermediate (Gilbert and Dressler, 1969; Knippers et al, 1969; Dressler, 1970; Koths and Dressler, 1978; Schroeder andKaerner, 1972; Godson, 1977; Ray, 1969)
Complex, which w e have purified to homogeneity and characterized
The rolling circleintermediate is characterized by a positive strand longer than unit length, which is generated by the covalent addition of nucleotides to thneicked positive strand of a duplex ring
Summary
Positive strand synthesisin the small, single-stranded DNA phages takes place in a rolling circle intermediate (Gilbert and Dressler, 1969; Knippers et al, 1969; Dressler, 1970; Koths and Dressler, 1978; Schroeder andKaerner, 1972; Godson, 1977; Ray, 1969). The electron microscopic analysis indicates that during the late life cycle synthesis of positive strand DNA, the single-stranded tail of the rolling circle intermediate is enclosed within a structure that appears to be a preformed phage capsid. This view is solidified in the following experiments, in which the DNA and protein components of the complex were studied separately. Aliquots of the mixture are spread for darkfield electron microscopy as previously described (Wolfson et al, 1972; Koths and Dressler, 1978)
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.