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Mismatch repair in recombination of bacteriophage T4
Abstract:
Abstract The review focuses on the mechanism of mismatch repair in bacteriophage T4. It was first observed in T4 as an extra recombination mechanism, which contributed to the general recombination only when particular rII mutations were used as genetic markers (high-recombination markers), whereas it was inactive toward other rII mutations (low-recombination markers). This marker-dependent recombination pathway was identified as a repair of mismatches in recombinational heteroduplexes. Comparison of the structure of markers enabled us to make several specific conclusions on the nature of the marker discrimination by the mismatch repair system operating during T4 crosses. First, heteroduplexes with one mismatched base pair (either of transition or of transversion type) as well as single-nucleotide mismatches of indel type are not efficiently repaired. Second, among the repairable mismatches, those with two or more contiguous mismatched nucleotides are the most effectively repaired, whereas insertion of one correct pair between two mismatched ones reduces the repairability. Third, heteroduplexes containing insertion mutations are repaired asymmetrically, the longer strand being preferentially removed. Fourth, the sequence environment is an important factor. Inspection of the sequences flanking mismatches shows that runs of A:T pairs directly neighboring the mismatches greatly promote repair. The mismatch is recognized by T4 endonuclease VII and nicked on the 3' side. The nonpaired 3' terminus is attacked by the proofreading 3'→5' exonuclease of T4 DNA polymerase that removes the mismatched nucleotides along with several (~25) complementary nucleotides (the repair tract) and then switches to polymerization. The residual nick is ligated by DNA ligase (gp30). Most probably, the T4 system repairs replication and other mismatches as well; however, it might not discriminate old and new DNA strands and so does not seem to be aimed at repair of replication errors, in contrast to the most commonly studied examples of mismatch repair.
Insights
Bacteriophage T4 mismatch repair fixes DNA errors during recombination, particularly with specific markers. It efficiently repairs multiple mismatches and is influenced by DNA sequences, involving T4 endonuclease VII and T4 DNA polymerase.
Area of Science:
- Molecular Biology
- Genetics
- Virology
Background:
- Mismatch repair (MMR) is a crucial DNA repair system.
- In bacteriophage T4, MMR was initially observed as a marker-dependent recombination mechanism.
- This pathway repairs mismatches in recombinational heteroduplexes.
Purpose of the Study:
- To elucidate the mechanism of mismatch repair in bacteriophage T4.
- To understand the discrimination of different mismatch types by the T4 MMR system.
- To identify factors influencing the efficiency of T4 mismatch repair.
Main Methods:
- Analysis of marker structures in T4 crosses.
- Comparison of repair efficiency for various mismatch types (single base, indel, contiguous mismatches).
- Investigation of sequence context effects on repair.
- Identification of key enzymes involved: T4 endonuclease VII, T4 DNA polymerase (3'→5' exonuclease), and DNA ligase (gp30).
Main Results:
- Single base mismatches and small indels are poorly repaired.
- Contiguous mismatches (≥2 bp) are repaired more efficiently than single mismatches.
- Insertion mutations are repaired by asymmetric removal of the longer strand.
- AT-rich sequences flanking mismatches enhance repair.
- T4 endonuclease VII nicks the mismatched strand, followed by exonuclease and polymerase activity, and ligation.
Conclusions:
- The T4 MMR system exhibits specific substrate preferences, favoring longer contiguous mismatches.
- Sequence context, particularly AT-rich regions, significantly impacts repair efficiency.
- The T4 MMR mechanism involves a coordinated action of endonuclease, exonuclease, and ligase.
- Unlike other systems, T4 MMR may not distinguish between old and new DNA strands, suggesting a different role than repairing replication errors.
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