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Functional complementation between chromosomal and plasmid mutagenic DNA repair genes in bacteria
S G Sedgwick1, D Lodwick, N Doyle
1Genetics Division, National Institute for Medical Research, London, UK.
Summary
Investigating DNA repair operons like umuDC, mucAB, and impCAB revealed subunit interchangeability in bacteria. Specific protein sequence conservation dictates functional interactions, explaining differences in induced mutagenesis.
Area of Science:
- Microbiology
- Molecular Biology
- Genetics
Background:
- The umuDC operons (E. coli, S. typhimurium) and analogous plasmid operons (mucAB, impCAB) are crucial for DNA repair and induced mutagenesis.
- These operons play vital roles in cellular responses to DNA damage caused by radiation and chemicals.
Purpose of the Study:
- To examine the interrelationships of these mutagenic DNA repair operons.
- To investigate the functional interchangeability of operon subunits in conferring UV resistance and UV mutability phenotypes.
- To compare DNA and protein sequences between these operons and the samAB operon.
Main Methods:
- In vivo functional tests of subunit interchangeability.
- DNA and protein sequence comparisons.
- Analysis of UV resistance and UV mutability phenotypes.
Main Results:
- E. coli and S. typhimurium umu operon components were reciprocally interchangeable.
- Certain heterologous combinations (e.g., mucA and impB) showed mutagenic responses.
- Higher protein sequence conservation correlated with functional subunit interactions.
- The E. coli umuD44 mutation dominated over umuD.
- S. typhimurium umuD's poor activity was linked to S. typhimurium umuC, not an inherent defect.
Conclusions:
- Functional interactions within mutagenic DNA repair operons are determined by specific protein sequence features.
- The interplay between umuD and umuC subunits in S. typhimurium limits induced mutability.
- Understanding these operon dynamics provides insights into bacterial DNA repair mechanisms and evolution.