Two types of recombination hotspots in bacteriophage T4: one requires DNA damage and a replication origin and the other does not.
Recombination hotspots have previously been discovered in bacteriophage T4 by two different approaches, marker rescue recombination from heavily damaged phage genomes and recombination during co-infection by two undamaged phage genomes. The phage replication origin ori(34) is located in a region that has a hotspot in both assays. To determine the relationship between the origin and the two kinds of hotspots, we generated phage carrying point mutations that should inactivate ori(34) but not affect the gene 34 reading frame (within which ori(34) is located). The mutations eliminated the function of the origin, as judged by both autonomous replication of plasmids during T4 infection and two-dimensional gel analysis of phage genomic replication intermediates. As expected from past studies, the ori(34) mutations also eliminated the hotspot for marker rescue recombination from UV-irradiated genomes. However, the origin mutations had no effect on the recombination hotspot that is observed with co-infecting undamaged phage genomes, demonstrating that some DNA sequence other than the origin is responsible for inflated recombination between undamaged genomes. The hotspots for marker rescue recombination may result from a replication fork restart process that acts upon origin-initiated replication forks that become blocked at nearby DNA damage. The two-dimensional gel analysis also revealed phage T4 replication intermediates not previously detected by this method, including origin theta forms.
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Related Subject Headings
- Ultraviolet Rays
- Replication Origin
- Recombination, Genetic
- Point Mutation
- Plasmids
- Mutation
- Molecular Sequence Data
- Models, Genetic
- Genome
- Electrophoresis, Gel, Two-Dimensional
Citation
Published In
DOI
ISSN
Publication Date
Volume
Issue
Start / End Page
Location
Related Subject Headings
- Ultraviolet Rays
- Replication Origin
- Recombination, Genetic
- Point Mutation
- Plasmids
- Mutation
- Molecular Sequence Data
- Models, Genetic
- Genome
- Electrophoresis, Gel, Two-Dimensional