Mouse polyoma virus and adenovirus replication in mouse cells temperature-sensitive in DNA synthesis
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Updated: Oct 14, 2026

Dissection of Adult Mouse Utricle and Adenovirus-mediated Supporting-cell Infection
Published on: March 28, 2012
Abstract:
Mouse adenovirus multiplies, apparently without impediment, in temperature-inactivated ts A1S9, tsC1 and ts2 mouse fibroblasts. Thus, the DNA of mouse adenovirus can replicate in the absence of functional DNA topoisomerase II, a DNA-chain-elongation factor, and a protein required for traverse of the G1/S interface, respectively, encoded in the ts A1S9, tsC1 and ts2 genetic loci. These results are compared with those obtained with polyoma virus.
Insights
Mouse adenovirus replicates in mouse cells lacking key DNA replication factors. This suggests viral DNA replication is independent of DNA topoisomerase II and G1/S interface traverse proteins.
Area of Science:
- Virology
- Molecular Biology
- Cell Biology
Background:
- Mouse adenovirus is a common viral agent in laboratory mice.
- Cell cycle progression is crucial for viral DNA replication in many viruses.
- Specific genetic loci (tsA1S9, tsC1, ts2) encode essential host factors for DNA replication and cell cycle progression.
Purpose of the Study:
- To investigate the replication mechanism of mouse adenovirus in host cells with impaired DNA replication machinery.
- To determine if mouse adenovirus DNA replication is dependent on host DNA topoisomerase II and G1/S interface proteins.
Main Methods:
- Utilizing temperature-sensitive mutant mouse fibroblast cell lines (tsA1S9, tsC1, ts2) with defects in DNA replication and cell cycle.
- Infecting these mutant cells with mouse adenovirus at non-permissive temperatures.
- Observing and quantifying viral multiplication and DNA replication.
Main Results:
- Mouse adenovirus successfully replicated in tsA1S9, tsC1, and ts2 mouse fibroblasts, even at temperatures where host cell DNA replication was inhibited.
- Viral DNA replication proceeded without impediment in the absence of functional DNA topoisomerase II, a DNA-chain-elongation factor, and a protein essential for G1/S interface traverse.
Conclusions:
- Mouse adenovirus DNA replication is independent of critical host cell DNA replication and cell cycle control factors.
- These findings offer insights into the unique replication strategies of adenoviruses and can be compared to other viruses like polyoma virus.
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