Replication of Mu prophages lacking the central strong gyrase site
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Updated: Aug 23, 2026

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Published on: August 21, 2016
1Department of Microbiology, University of Colorado Health Sciences Center, 4200 E, 9th Ave., Denver, CO, USA. martin.pato@uchsc.edu
Abstract:
Replication of Mu prophages lacking the central strong gyrase site (SGS) is severely slowed. To study details of the replication of these prophages, an assay was developed for determining the rate and extent of introduction of nicks at the 3'-ends of a Mu prophage, an early step in Mu replicative transposition. The maximal level of end-nicking of a prophage with the SGS, about 70-90% depending upon the host strain, was achieved within about 15 min after induction, whereas at that time less than 5% nicking was observed with a prophage lacking the SGS. The amount of nicking at the end of the SGS(-) prophage increased with time, and approx. 30% nicking of the SGS(-) prophage was achieved by 60 min post-induction. Nicking kinetics were identical at each end of the prophages, and no nicking was observed at the 5'-ends of the prophages, verifying in vivo the earlier results with in vitro systems. To determine if prophage location affects the kinetics of replication, we examined prophages at numerous chromosomal locations. SGS(+) prophages at different chromosomal locations showed essentially identical replication kinetics. SGS(-) prophages showed a range of delays in replication and host lysis. A gradient of delays was apparent, with prophages further from the chromosomal origin of replication, oriC, showing longer delays than ones nearer to oriC. However, there were also exceptions to this overall gradient. Possible explanations for the differences in the delays observed with SGS(-) prophages are discussed.
Insights
Replication of Mu prophages lacking the strong gyrase site (SGS) is slowed due to delayed nicking. Prophage location influences replication, with those farther from oriC showing longer delays.
Area of Science:
- Molecular Biology
- Virology
- Genetics
Background:
- Bacteriophage Mu replication is crucial for its life cycle.
- The strong gyrase site (SGS) plays a role in Mu prophage replication efficiency.
Purpose of the Study:
- To investigate the role of the SGS in Mu prophage replication kinetics.
- To develop an assay for measuring nicking at prophage ends during replication.
- To determine the impact of chromosomal location on SGS-deficient prophage replication.
Main Methods:
- Development of an assay to quantify 3'-end nicking in Mu prophages.
- Comparison of nicking kinetics between SGS-containing and SGS-deficient prophages.
- Analysis of replication and lysis timing for prophages at various chromosomal positions.
Main Results:
- Prophages lacking SGS exhibit significantly reduced 3'-end nicking compared to SGS(+) prophages.
- Nicking of SGS(-) prophages increases over time but remains lower than SGS(+) prophages.
- Replication and lysis of SGS(-) prophages are delayed, with delays correlating with distance from the chromosomal origin (oriC), though exceptions exist.
Conclusions:
- The SGS is essential for efficient early-stage nicking during Mu replication.
- Chromosomal location influences the replication kinetics of SGS-deficient Mu prophages.
- The findings provide insights into the mechanisms of bacteriophage replication and host-prophage interactions.
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